| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs34988080 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147983188 | TTTTTTTTTTTTTTT[-/T]GAAGCAGAGTCTCAC | 79658 |
| rs34997883 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147970921 | GGCAAAACCCCATCT[C/T]TACTTAAAAGAAAGT | 79658 |
| rs35002847 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147991142 | CATGTGTACCCCTGA[A/C]CCTAAAAAAAAAAAA | 79658 |
| rs35032347 | in-del | -/GA | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148059993 | AGAGAGAGAGAGAGA[-/GA]GGGGAGAGAGAGGAG | 79658 |
| rs35037019 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147902944 | TGTGTGGGGCAGGCT[-/T]ATATACTTTCCAAAA | 79658 |
| rs35038176 | snp | A/T | 0.365439 | 0.221752 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148049010 | TCAGAAACTTGATTT[A/T]TTTTTTTCTGTGCCA | 79658 |
| rs35046542 | in-del | -/A | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147927298 | TTAAGCCATTCTAAA[-/A]GTTAGACCTGCCTTT | 79658 |
| rs35053440 | in-del | -/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147836463 | ACTAGTCGATTTGGG[-/G]ATATATACTTTAAAA | 79658 |
| rs35055570 | in-del | -/A | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147838019 | ATTTACTTGATTAAA[-/A]TATGTGTCCATATTT | 79658 |
| rs35056453 | snp | G/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147985733 | CCTTGTCATTCCTGG[G/T]TCTGAGAAAATACAT | 79658 |
| rs35080016 | in-del | -/A | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147820644 | GCCTAGGCTGGAGTT[-/A]CAGTGGCATGATCTT | 79658 |
| rs35088268 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147930526 | TACTCTCTTTTAATT[C/T]TAATTGTCTGTTTAA | 79658 |
| rs35089971 | in-del | -/A | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147879489 | TGTTTTTGAGTGAAA[-/A]TGGGCCAGAAGACAG | 79658 |
| rs35099145 | in-del | -/T | 0.453209 | 0.145623 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147836654 | TGGGTTCCTTAAATC[-/T]TAAGTACCAAGTAAG | 79658 |
| rs35101234 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147826885 | TGCCTCTTTCCCTCC[C/T]CAAGCCCCGCCCTCA | 79658 |
| rs35106992 | in-del | -/A | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147746044 | TTCCCGCCTCTGCCT[-/A]CCCAAAGTGCTGGGA | 79658 |
| rs35115631 | snp | C/T | 0.217551 | 0.247885 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147834420 | GCTGCAGAGAGCTAT[C/T]ATTGTGCCACTGCAC | 79658 |
| rs35116202 | in-del | -/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147733896 | TTTTGTTTTTAAGTC[-/C]TCTGCTGCTTGAATC | 79658 |
| rs35131588 | snp | C/T | 0.251014 | 0.249998 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148052272 | AGAGGGCTTCCTCAA[C/T]CCCAGCACTCCTTGA | 79658 |
| rs35133175 | snp | C/T | 0.227369 | 0.248974 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147972669 | CAAGGATGCCAGATA[C/T]GTCCCATGAGATGGG | 79658 |
| rs35148494 | in-del | -/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148006620 | TTGTGAATTTGATTT[-/C]CCCTGTTGACTTACT | 79658 |
| rs35151398 | in-del | -/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147890296 | AGCCATTACTACTTT[-/G]ATTATCAATGGTTAG | 79658 |
| rs35175853 | in-del | -/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147962194 | TGGTGGAATTGGCCC[-/C]TGTTGCCAGACTACC | 79658 |
| rs35177834 | in-del | -/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147990071 | CTCCTGATATTCAGC[-/G]CTTCTGCCTGAATGA | 79658 |
| rs35192758 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148010546 | CCTTTATAGTATAAT[-/T]CTATTATTGCTATTT | 79658 |
| rs35196280 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147886252 | AATTCTGCTCTTTTT[-/T]ACAAGTCTTGGTAAT | 79658 |
| rs35217152 | in-del | -/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148021401 | TCTGTCCATCACCAG[-/G]TTGTTGGGATATAAC | 79658 |
| rs35222813 | in-del | -/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147906052 | TTATTTGTGTATAAG[-/C]AATGCTTGTGATTTT | 79658 |
| rs35243600 | snp | A/T | 0.379746 | 0.213696 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147881622 | CAGCCTGGGTGAAAG[A/T]GCGAGGCTCCCTTCT | 79658 |
| rs35278062 | in-del | -/T/TTT | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148012940 | TTTTTTTTTTTTTTT[-/T/TTT]AAACCTTCTTTAAAG | 79658 |
| rs35295439 | in-del | -/CCC | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148032344 | CCCCCCCCCCCCCCC[-/CCC]ATATTGTAGGCCAAA | 79658 |
| rs35305706 | in-del | -/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147972119 | GTTCAAGATAAGTCC[-/C]ATTAGACAGAGATTT | 79658 |
| rs35309386 | in-del | -/T | 0.454544 | 0.143743 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147947944 | TCCTACCTGCCACTG[-/T]TTTTTTTTTTTTTTT | 79658 |
| rs35315585 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147914953 | AACAGGCTATTTCTG[G/T]AGGTTGACATTCTCT | 79658 |
| rs35317484 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147920913 | AACTTGGTTGTGAAG[C/G]AAACATGGAGAAACA | 79658 |
| rs35323687 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147833550 | GAAAAACCAGATTTT[-/T]GATGACTGAGATGAA | 79658 |
| rs35339331 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147833173 | TATGTGTGGTGATAC[A/G]GTTTGGCTCTGTGTC | 79658 |
| rs35344532 | in-del | -/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147971239 | GGGGTTGTGCCTTAG[-/G]ATTTGTGAGTTTTGC | 79658 |
| rs35344745 | snp | C/T | 0.251014 | 0.249998 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148061070 | AAACACACCCACCCA[C/T]CCGCGGGTGTTTTCA | 79658 |
| rs35350473 | snp | G/T | 0.264906 | 0.249555 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148050264 | ATTTCTTATTTTAAT[G/T]ATGTATTTATAGAAA | 79658 |
| rs35371855 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147921784 | TCCCACCTGCCGTCT[A/C]TGTGTGACATCTGGC | 79658 |
| rs35420361 | in-del | -/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147962968 | CCTGGCCACCACTCC[-/C]TTTCATTTCTTTTTT | 79658 |
| rs35435758 | in-del | -/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148012499 | ACTTAAGTTGACAGG[-/C]AGTGAGAGGGGGAAC | 79658 |
| rs35438984 | in-del | -/A | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147825447 | CTCAAAAAAAAAAAA[-/A]GTGACAGAGACATAT | 79658 |
| rs35449374 | in-del | -/T/TTTT | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148052412 | TTTTTTTTTTTTTTT[-/T/TTTT]GGGCTAATTGACCAA | 79658 |
| rs35454464 | in-del | -/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147771349 | TGGGTACACAGTAGG[-/G]TATATATATTTGTGG | 79658 |
| rs35456613 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147900015 | AATAATGTCTCCTTA[A/G]ACTTGTGAATGTTTC | 79658 |
| rs35457654 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147919468 | CCGGCTCTACCACTA[A/G]GAAGTGACTGCTTTT | 79658 |
| rs35458775 | in-del | -/AGTGTTTT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147751712 | TCAGAGACTGTGCCC[-/AGTGTTTT]CACAGGAGTTAGCAT | 79658 |
| rs35463632 | in-del | -/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147780024 | GTATCTTTAATTTTT[-/G]CTGGAAGTTACTAAT | 79658 |
| rs35466591 | in-del | -/TCTT | 0.310386 | 0.242597 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147917839 | TTACTCAGAGGTCTT[-/TCTT]AAAGTCGCATTTATT | 79658 |
| rs35472561 | in-del | -/TA | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148017653 | TTATGAGCCAGTAAC[-/TA]TATATATATATATAT | 79658 |
| rs35472809 | in-del | -/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147978996 | CAGATATTTTCTCCC[-/C]GTTTTGTAGATTGTC | 79658 |
| rs35482083 | in-del | -/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147934585 | CTTGCCTGTAATCCC[-/C]AGCACTTTGGGATGC | 79658 |
| rs35484289 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147924724 | TTGATTGTAATCTCA[A/G]TTTTACTCCTTATTA | 79658 |
| rs35486212 | in-del | -/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147870481 | AAACTTTATAATCAG[-/C]AAAAAGGTAAAAGGT | 79658 |
| rs35490978 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147742751 | CGGCCTCCCAAAGTT[C/T]TAGGATTACAGGCAT | 79658 |
| rs35503875 | in-del | -/T | 0.488545 | 0.074807 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148061614 | CTTAGAAGAATAATG[-/T]TTTTTTTTTTTAAAT | 79658 |
| rs35519368 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148035223 | GTCATAGTAGCTTTT[-/T]GGGCAAGCATTATGC | 79658 |
| rs35521843 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147924571 | GGTGTTTTTAGAACA[G/T]AAGAAACTTGGTGGA | 79658 |
| rs35524232 | in-del | -/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147861324 | CACGGTGGCACCCGG[-/G]AAACTTGGAGACACC | 79658 |
| rs35525596 | in-del | -/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147845073 | CCTTTTGACATTCCC[-/C]TGTAATGCTCAAACT | 79658 |
| rs35527038 | snp | C/T | 0.251859 | 0.249993 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148049252 | AGGATTCTGTAGGTC[C/T]GAGAAGGGTCCTGAG | 79658 |
| rs35546204 | in-del | -/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148065445 | TCAGAGACAGAGACT[-/C]CCTGGTAGTGTCAGA | 79658 |
| rs35548212 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147924574 | GTTTTTAGAACAGAA[C/G]AAACTTGGTGGAACT | 79658 |
| rs35571591 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147850660 | CCATCTTTAAGAACT[-/T]GTAACACTCACTGCG | 79658 |
| rs35623963 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147830699 | TAATTTTTGTATTTT[-/T]AGTAGAGACGGGGTT | 79658 |
| rs35636277 | in-del | -/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147963072 | AGGCATACCTTCCCC[-/C]AAATATAACTCTATT | 79658 |
| rs35640507 | in-del | -/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147879521 | CAATATATATGTTTT[-/G]CTGAATTACATGCAT | 79658 |
| rs35642916 | in-del | -/A | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147902752 | CTCAAAAATAAAGAA[-/A]GGGGAGGGGAAGGGA | 79658 |
| rs35679243 | in-del | -/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147767380 | ATCTTTTTTTTTTTT[-/T]AATCCACATGGCAAA | 79658 |
| rs35691766 | in-del | -/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147868885 | CCTGCCATGTGACCC[-/C]GGTTCCTAACAGGCC | 79658 |
| rs35695401 | snp | A/G | 0.0970103 | 0.197722 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147883233 | AATATGAAAGAGAAT[A/G]TCAGTGAAAAAGAGG | 79658 |
| rs35696967 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147984853 | GGCCAATCTGTGGAG[C/T]GCACAGTGGTCTGAG | 79658 |
| rs35707046 | in-del | -/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148046240 | AATAAAATGGTCCCC[-/C]TGTGAATGGATACAT | 79658 |
| rs35709427 | in-del | -/A | 0.0748431 | 0.178382 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147737483 | TTGATAAAGTGGTGT[-/A]AATTGTAAATTTTGT | 79658 |
| rs35711281 | in-del | -/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147842214 | GCTAGGGTTATGGGG[-/G]TGTGAGCCACCATGC | 79658 |
| rs35719237 | in-del | -/GA | 0.392881 | 0.205147 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148060027 | GAGACGAGAGAGAGA[-/GA]CGAGAGACAGATATG | 79658 |
| rs35721766 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147850840 | CTCCTTCACCCTTTT[-/T]GAGCTTGGCACTTAT | 79658 |
| rs35738981 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147982571 | TTTTTTTTTTTTTTT[G/T]GGGATTTTGTGTTGA | 79658 |
| rs35739014 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147967718 | TTGCAACAGAGACCA[A/G]ATAGCCCGCAAGGCA | 79658 |
| rs35740795 | in-del | -/CT | 0.206336 | 0.246157 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148014769 | GTCTGCTATGCATCA[-/CT]CTATTTAGCGTATAG | 79658 |
| rs35761456 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147928399 | GAGTCTCTGGTTTGT[G/T]TGGGAGTGGGAAGAC | 79658 |
| rs35774782 | in-del | -/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147763771 | TTTTTTTTTTTTTTT[-/T]AAAAACAGAGTTTTG | 79658 |
| rs35780665 | in-del | -/A | 0.444444 | 0.157135 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147906546 | AAAGTAAAAAAAAAA[-/A]TGGTTACAACAGTTA | 79658 |
| rs35799308 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147919323 | AAAAACTCCATTTTG[C/T]TACAGTATCAGCATA | 79658 |
| rs35810358 | snp | C/T | 0.438386 | 0.164349 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147866045 | TGGGAATGGAGCCTG[C/T]TGGGTGTCAGAGCCC | 79658 |
| rs35819831 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147824245 | GAGAATTGCTTGAAT[A/C]TGGGAGATGGAGGTT | 79658 |
| rs35830686 | in-del | -/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147844924 | GCTTGAAAACCCTCC[-/C]TGTGGCTTTCCACTG | 79658 |
| rs35835995 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148050559 | TTTGTGTTTTTAGTA[A/G]AGACGGGGTTTCACT | 79658 |
| rs35857601 | in-del | -/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147744798 | CCAGGAGACATGTTC[-/C]AGTAGTGTGTTTCTT | 79658 |
| rs35862342 | in-del | -/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148043723 | GTATATGCATTTTTC[-/C]ATATATATATGTGTA | 79658 |
| rs35864245 | in-del | -/TT/TTTT/TTTTTT | 0.146314 | 0.227484 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147869996 | AAAAAGTCCCAGTTT[-/TT/TTTT/TTTTTT]GTGTGTGTGTGTGTG | 79658 |
| rs35887819 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147954419 | TTTTGGCTTCATGAT[C/G]AGTTGACACTTTTGT | 79658 |
| rs35899247 | snp | A/T | 0.379746 | 0.213696 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147881608 | CTGCCACTGCACTCC[A/T]GCCTGGGTGAAAGAG | 79658 |
| rs35904603 | in-del | -/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148054055 | TGCATCAGTCATTTT[-/G]TGGTTTTTAGTTTAA | 79658 |
| rs35906862 | in-del | -/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148008088 | GTGGCCTCATCCTAG[-/G]CTTCCTGTTTATGTT | 79658 |
| rs35906887 | in-del | -/G | 0.119281 | 0.213102 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147788138 | TAAAAAATTTGATTT[-/G]TTTTTTTTTAAAAAG | 79658 |
| rs35941586 | in-del | -/AAA | 0.0759472 | 0.179459 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147751191 | CTCAAAACCAAAAAC[-/AAA]AAAAACAAACAATGA | 79658 |
| rs35956876 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147764062 | ACCATGCCTGGCCCA[A/G]ACAGTGATTCTTGAT | 79658 |
| rs35975487 | snp | A/G | 0.160577 | 0.23346 | synonymous-codon, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148023316 | CACCTGCCTGTCAGC[A/G]TCACCCCCAAATGCG | 79658 |
| rs35977132 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147942787 | TGATGAGAGGGTATT[C/T]TTAGTTGTCTTCCCC | 79658 |
| rs35980618 | snp | G/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147925638 | ATACTAGAAATATGG[G/T]TCCTGTTCTTAAAGA | 79658 |
| rs35994502 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147983366 | AATTTTTTGTATTTT[-/T]AGTAGAGACAGGGTT | 79658 |
| rs36025358 | in-del | -/A | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148005928 | CAATATTAGGTGAAA[-/A]CAAATACATGTATCT | 79658 |
| rs36025529 | in-del | -/T | 0.480539 | 0.0967035 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147753355 | TTCTTTTTTTTTTTT[-/T]GAGACACAGTCTGTT | 79658 |
| rs36033014 | in-del | -/A | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147833911 | GGGCACCTCTCAGAT[-/A]AGAGGAAGGAGGAGT | 79658 |
| rs36037094 | in-del | -/T | 0.287085 | 0.247234 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147803026 | AGTTTTGTTTATTGC[-/T]TTTTTTTTTTGAGAT | 79658 |
| rs36067753 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148059522 | AAGGACTCTCAAAAA[-/T]TTTCATTATGTTCTA | 79658 |
| rs36114707 | in-del | -/ACA | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147900845 | ACAACAACAACAACA[-/ACA]CGCCTTGAGACAGGT | 79658 |
| rs36133786 | in-del | -/CA | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147783817 | TATTTATATAACACA[-/CA]TTAAATTGTGTATTA | 79658 |
| rs36202812 | in-del | -/TATATAT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147784662 | ATATATATTATAAAA[-/TATATAT]TATATATTATAAATA | 79658 |
| rs36205660 | in-del | -/AA | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147872119 | AAAAAAAAAAAAAAA[-/AA]GCCTTCCATTCCCAG | 79658 |
| rs36217593 | in-del | -/GT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911995 | TTTAAGAACATTCAC[-/GT]GTGTGTGTGTGTGTG | 79658 |
| rs41280455 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148064649 | TGGATTAAGCGGCTG[C/T]GTTAGGCTCCCAGAC | 79658 |
| rs41320648 | snp | C/T | 0.077417 | 0.180873 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148006348 | ATGACGTGGGGAAAA[C/T]GGAGGCACCCAGCTG | 79658 |
| rs41435251 | snp | A/G | 0.0700422 | 0.173537 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147927977 | CTCGGCACTTTGCCA[A/G]TAGCTTGGGTAGAAA | 79658 |
| rs41515750 | snp | C/T | 0.114036 | 0.209795 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147925398 | TCTTGCAAAAAGCAA[C/T]GGCCCACTTTTGCCT | 79658 |
| rs55650760 | snp | A/G | 0.475613 | 0.107697 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147902494 | GCACTTTAGGAGGCC[A/G]AGGTGGGCCGATCAC | 79658 |
| rs55657699 | snp | C/T | 0.0788843 | 0.182262 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147899108 | AGTCCTGCTCTCAGA[C/T]TTCCTCATGAGCGCT | 79658 |
| rs55689306 | snp | A/G | 0.0912534 | 0.193131 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147847081 | GGATGGAAGAGGGAA[A/G]TGAAATACTAATTTT | 79658 |
| rs55706053 | snp | G/T | 0.154993 | 0.231244 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147746884 | AGATGACAAGATTCA[G/T]TAATTCTGTTTTAAT | 79658 |
| rs55714518 | snp | A/G | 0.27008 | 0.249192 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147805220 | GTTCCAGCACTGTTT[A/G]CTGAATAGGGAGTCC | 79658 |
| rs55752555 | snp | A/G | 0.409212 | 0.192748 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147937256 | CTCTGGCATGGGGAT[A/G]GCTGTCTTCTCCCTG | 79658 |
| rs55771362 | snp | C/G | 0.0788843 | 0.182262 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147898964 | CCTTACACCAGATCC[C/G]TTTCTCGACATGTGG | 79658 |
| rs55820558 | snp | G/T | 0.413748 | 0.188909 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147898965 | CTTACACCAGATCCC[G/T]TTCTCGACATGTGGG | 79658 |
| rs55881523 | snp | G/T | 0.0941369 | 0.195465 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147985178 | CACAAGAAGGGAAGG[G/T]TAGCTCTGGCTGCAG | 79658 |
| rs55888188 | in-del | -/A | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148003380 | GTGGTGCTGAGAAGA[-/A]TTTATATTCTGTCGA | 79658 |
| rs55902656 | in-del | -/CTGCCCA | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911208 | GAAAACCACTGCCCA[-/CTGCCCA]ATTCATTAAAATTCT | 79658 |
| rs55912417 | snp | A/G | 0.258843 | 0.249844 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148005671 | CAGGTTTTAATTTGA[A/G]GAAACTTTAAACAGT | 79658 |
| rs56028529 | in-del | -/GTGTGTGTGT | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147912031 | TGTGTGTGTGTGTGT[-/GTGTGTGTGT]ATAGTTTTCTTTAAC | 79658 |
| rs56093867 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147846050 | GCTTTGTTGCCCCAG[C/T]TATTTTACACCCAAG | 79658 |
| rs56178834 | snp | C/G | 0.146314 | 0.227484 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147870006 | TCCCAGTTTGTGTGT[C/G]TGTGTGTGTGTGTGT | 79658 |
| rs56199012 | in-del | -/A | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147852734 | TTTTTTTTTTTTAAA[-/A]TGGAGCGGAGTTTCG | 79658 |
| rs56280979 | snp | A/G | 0.0865458 | 0.189163 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147998693 | TTTGAAAATACATTA[A/G]TATATCCTACTATTA | 79658 |
| rs56316266 | snp | G/T | 0.191461 | 0.24305 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148002683 | CCATTTCTTCTAGAT[G/T]TTCTAGTTTATTTGC | 79658 |
| rs56320153 | snp | A/G | 0.0930568 | 0.194599 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147990333 | ACTAAACATTTTGAC[A/G]AATGAATGTTAGCCA | 79658 |
| rs56320699 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148049804 | AAAATTGTTTTTTTT[G/T]TTTGTTTGTTTGTTT | 79658 |
| rs56356409 | snp | A/T | 0.242775 | 0.249896 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147793322 | TATATATATATATAT[A/T]TTTTTTTTTTTACAA | 79658 |
| rs56376203 | snp | C/G/T | 0.281577 | 0.247998 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147870002 | AAAGTCCCAGTTTGT[C/G/T]TGTGTGTGTGTGTGT | 79658 |
| rs56385546 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147863783 | GTTCATGTTAGCTTA[A/G]TAACACGTTATGTTT | 79658 |
| rs56401722 | snp | C/G | 0.029116 | 0.117091 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147985281 | ACGGTCTCTGCACAG[C/G]AAAGATGGGTGGCTC | 79658 |
| rs56407863 | snp | A/C/G/T | 0.0143052 | 0.0836363 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911584 | AGCCAGGATGGTCTT[A/C/G/T]ATCTCCTGACTTCGT | 79658 |
| rs56657155 | snp | C/T | 0.228253 | 0.249052 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147991567 | GCATCCTTTACCTAG[C/T]GTGTACCAAAATTCC | 79658 |
| rs56664679 | snp | C/T | 0.046775 | 0.145601 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147836530 | TCTGAAAGAATGAGG[C/T]ATTATTCAACAGCCA | 79658 |
| rs56670397 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147926557 | GATATTCTGAATGCA[A/G]GTGGCATGTTATAAG | 79658 |
| rs56740685 | in-del | -/A | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147867886 | AAAAAAAAAAAAAAA[-/A]GTTGAGAGTGAATAC | 79658 |
| rs56742479 | snp | C/T | 0.121717 | 0.214577 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147886587 | TTTTAATACCCTTCA[C/T]TCCACTGCTTCTTTC | 79658 |
| rs56743769 | snp | C/T | 0.0984431 | 0.198823 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147981205 | GTTTTGTGCAGTAAA[C/T]GTTCCTCTTAACATT | 79658 |
| rs56756471 | snp | C/T | 0.0792508 | 0.182605 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147886590 | TAATACCCTTCACTC[C/T]ACTGCTTCTTTCCTT | 79658 |
| rs56763356 | in-del | -/T | 0.267908 | 0.249358 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147976542 | CTGTTTTGTGTGTGG[-/T]TTTTTTTTTTTTTTC | 79658 |
| rs56781517 | in-del | -/TT | | | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147781697 | TTTTTTTTTTTTTTT[-/TT]GAGACAGTCTTGCTC | 79658 |
| rs56814891 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147939695 | AAACACTTGATTTTT[C/T]CAAAGGTTATTTTTA | 79658 |
| rs56834952 | snp | A/G | 0.293807 | 0.246132 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147970941 | TAAAAGAAAGTACAA[A/G]AATTAGCCAGGCGTG | 79658 |
| rs56912243 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147778443 | CCTGTTGGAGACCTG[C/T]CTGCCAAGGGCACAG | 79658 |
| rs56946313 | snp | A/G | 0.294064 | 0.246086 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147742677 | TTTTAGTAGAGATGG[A/G]GTTTCACCATGTTTG | 79658 |
| rs56946602 | in-del | -/TTTT | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147830535 | TTTTTTTTTTTTTTT[-/TTTT]GATGGGGGGAGCCTT | 79658 |
| rs56995861 | in-del | -/A | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147793322 | ATATATATATATATT[-/A]TTTTTTTTTTTACAA | 79658 |
| rs57021076 | in-del | -/ATAT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147793240 | TGTGTGTGTGTATAT[-/ATAT]GTATGGTAGGTGTTT | 79658 |
| rs57021418 | snp | A/T | 0.261608 | 0.24973 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148006689 | AAAAGGGAACATTTT[A/T]AAAAGATTATGTGTT | 79658 |
| rs57058691 | in-del | -/TT | 0.194278 | 0.243711 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147867927 | GATTTTGTTTCTAAC[-/TT]TTTTTTTTTTTTATG | 79658 |
| rs57062177 | in-del | -/A | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147793145 | CTCTCTGGAAAAAAA[-/A]GAAAATGTGTGTGTA | 79658 |
| rs57095399 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147769448 | GGTATAATATACATT[A/T]AAAATTGTGCATCAA | 79658 |
| rs57114670 | in-del | -/C | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147893063 | TTGAATGGAAGTAAA[-/C]TTTTTTTTTTTTTGA | 79658 |
| rs57188427 | in-del | -/A | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147793324 | ATATATATATATTTT[-/A]TTTTTTTTTACAAAT | 79658 |
| rs57194632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147937800 | GCCTGACCAACATGG[C/T]GAAACCCCATCTCTA | 79658 |
| rs57348496 | in-del | -/GTGTGTGTGTGTGTGT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147870960 | TGTGTGTGTGTGTGT[-/GTGTGTGTGTGTGTGT]TTGAGATGGAGTCTT | 79658 |
| rs57395713 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147754717 | AACATAAAGCAAAAT[A/T]ACAGGAAAAAGACAA | 79658 |
| rs57423070 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148025498 | TGCCCTCAGTTTTTT[A/G]TAGTTAAGTTTTAGT | 79658 |
| rs57437177 | snp | A/G | 0.377187 | 0.215229 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147966960 | TCTTTCATTCTCACT[A/G]TGATGAGCTTGGTTC | 79658 |
| rs57521374 | in-del | -/CTTTT | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147953641 | TTGTTTGTTTTCTCT[-/CTTTT]ATTTCCTAATCATTC | 79658 |
| rs57534364 | in-del | -/TT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147820609 | TTTTTTTTTTTTTTT[-/TT]GAGACAGGGTCTCCC | 79658 |
| rs57536956 | snp | C/T | 0.196149 | 0.244131 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147993206 | CAGAGATACATTTAT[C/T]TAGAATTCTAGAGCA | 79658 |
| rs57544959 | snp | A/G | 0.089084 | 0.191327 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147907389 | TAGAAAACGCCACAG[A/G]ACCAATTTAAATAAA | 79658 |
| rs57572532 | in-del | -/ATATATATATATAT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147766826 | TATATATATATATAT[-/ATATATATATATAT]TTATTTATTTATTTA | 79658 |
| rs57613352 | in-del | -/A/AAA | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147824334 | TCAAAAAAAAAAAAA[-/A/AAA]TACGGATTCTTTTTT | 79658 |
| rs57627764 | in-del | -/AATTA | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147783181 | TTATATAACACATTA[-/AATTA]TATATTGTATAATTT | 79658 |
| rs57640571 | snp | G/T | 0.0637235 | 0.166737 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147876013 | TTTACAGTTTTCACT[G/T]CATTTAAGTGTGGCT | 79658 |
| rs57680318 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147855685 | TATTGTCAGATGGTT[G/T]TTTTTTTTTTTTTTT | 79658 |
| rs57726071 | snp | A/G | 0.142947 | 0.22592 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147906979 | TTGAGGAGGTCATCT[A/G]AATTCTCAATTTCAT | 79658 |
| rs57760152 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147756604 | TCATGTGCCATCCTG[C/T]TCCATCCCACCTGGG | 79658 |
| rs57795453 | in-del | -/A | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147784732 | ATAATATATTATAAA[-/A]TATATATTATAAATA | 79658 |
| rs57919251 | in-del | -/ATGAGTAT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148017683 | TATATATATATATAT[-/ATGAGTAT]GTGTGTGTATGTAAA | 79658 |
| rs57931206 | in-del | -/ATATATATAT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148043643 | TATATATATATATAT[-/ATATATATAT]TTTAGGTGTATAAAT | 79658 |
| rs57981912 | in-del | -/T/TT | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147878794 | TTTTTTTTTTTTTTT[-/T/TT]GAGTCGGAGTCTCGC | 79658 |
| rs57984081 | snp | C/T | 0.095934 | 0.196885 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147946112 | GCATGTATAGGCAAG[C/T]CTTATGTGCACAATG | 79658 |
| rs58014715 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148071488 | AGGCATGGTGGTGCG[C/T]GCCTGTAATCCCAGC | 79658 |
| rs58028291 | snp | G/T | 0.113334 | 0.209338 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147919593 | TTTTTTTTTTGTGGA[G/T]ATGCAGTCCCTCTCT | 79658 |
| rs58068435 | snp | C/T | 0.254385 | 0.249962 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147794646 | GTTATATGGTACATA[C/T]TTTGTTATGTTTCAT | 79658 |
| rs58111026 | snp | G/T | 0.0193772 | 0.0965046 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147770150 | CTTAGTATGAATGTT[G/T]TAATTGGAGAATCTG | 79658 |
| rs58165362 | snp | C/T | 0.0759472 | 0.179459 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148069087 | CGCGTAGACACTGCT[C/T]GGGGGAGGAGTGGTG | 79658 |
| rs58201461 | snp | G/T | 0.257454 | 0.249889 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147990119 | GATTGGAGGGCAGAT[G/T]AAGAAGGCACCCCGT | 79658 |
| rs58234592 | snp | A/G | 0.0626037 | 0.165477 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147890752 | GAATCACTTGAACCC[A/G]GGAGACGGAGGTTGC | 79658 |
| rs58265111 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147870004 | AGTCCCAGTTTGTGT[G/T]TGTGTGTGTGTGTGT | 79658 |
| rs58274809 | snp | C/T | 0.255782 | 0.249933 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147792016 | TATGATGTGTATGTG[C/T]GTTTCTCTGGGGACA | 79658 |
| rs58289718 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148061864 | TACTTGAAGGCATCA[A/G]AGAACAACCAGTATC | 79658 |
| rs58355236 | in-del | -/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147828558 | TTTCCAACATGCTTC[-/G]TGGTAATCAAGTGAT | 79658 |
| rs58357782 | snp | C/G | 0.261608 | 0.24973 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148001599 | TTTCATTGAGCAGTG[C/G]TTTATAGTTCTCCTT | 79658 |
| rs58379522 | in-del | -/A | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147881282 | TCAAAAAAAAAAAAA[-/A]GTAACATTGGTATTG | 79658 |
| rs58411489 | in-del | -/CC | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147759591 | CACCGCCCCCCCCCC[-/CC]TTTAAAAAGGAAACA | 79658 |
| rs58421633 | snp | A/C | 0.031825 | 0.122064 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147788679 | ACAGTGGGTTATAAA[A/C]AGTCTGATTATCTCA | 79658 |
| rs58443426 | snp | A/G | 0.0618563 | 0.164627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147909387 | TGAAGAGATTGGTGG[A/G]TAGGGCTGAAAGAAA | 79658 |
| rs58463407 | in-del | -/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148006005 | CGCAGAGATATGGGG[-/G]TCTAAGTATCTCTTT | 79658 |
| rs58497080 | snp | C/T | 0.229136 | 0.249128 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148028841 | AAATCGGGGACTTCT[C/T]AACTGACTAGATGGA | 79658 |
| rs58575818 | in-del | -/ATTTATTT | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147762521 | TTTATTTATTTATTT[-/ATTTATTT]TTATTTATTTATTTA | 79658 |
| rs58694083 | snp | A/C | 0.0726307 | 0.176182 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147966060 | TCACTGCACAGTGAT[A/C]CTGGGCTGAAAGAGT | 79658 |
| rs58710671 | snp | A/T | 0.084364 | 0.187256 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147991618 | GGTATTCAGCATGAC[A/T]ACTGCACATGCACAG | 79658 |
| rs58740360 | snp | A/G | 0.0633504 | 0.166319 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147880341 | CCCTGAAAAATATTT[A/G]AAGCAGCTTTTAATA | 79658 |
| rs58762227 | snp | C/T | 0.227664 | 0.249 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147802995 | TCTCTCCACTTTTTT[C/T]CCCTTAGTTTTGTTT | 79658 |
| rs58776118 | snp | A/G | 0.128632 | 0.218563 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147996339 | TGCCTCAGGAGAGGA[A/G]GGTGGGAAAGATGAA | 79658 |
| rs58833680 | in-del | -/A | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147931327 | AGAAAAAAAAAAAAA[-/A]CTTGGGGCCTGTAAA | 79658 |
| rs58858904 | in-del | -/CTCTTAGCCCCAG | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147733348 | CGGAATTAGCCCCAG[-/CTCTTAGCCCCAG]TGAGGAGCTGGGCAG | 79658 |
| rs58928158 | in-del | -/A | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148037848 | CAAAAAAAAAAAAAA[-/A]GAAAAGAATGGATGT | 79658 |
| rs58929565 | snp | A/G | 0.0633504 | 0.166319 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147880372 | AAAACACATTTATAT[A/G]ATAATGAAACAGACA | 79658 |
| rs58943146 | in-del | -/A | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148030882 | AAAAGAAAAAAAAAA[-/A]CCATTTAAGCCTATT | 79658 |
| rs58965352 | snp | C/T | 0.0562307 | 0.157967 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147747378 | CTAAAAATATCTTCT[C/T]TTGCTCTTTTCTAGC | 79658 |
| rs59020830 | snp | A/T | 0.0360663 | 0.129354 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147970267 | CAGCTGACCTAAGTA[A/T]ACCCTTCAGAGGATC | 79658 |
| rs59081829 | snp | A/G | 0.206642 | 0.246211 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147755257 | TTTTTACTTATTTTT[A/G]CTTGTTAAATTTTCT | 79658 |
| rs59091659 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147872145 | TCCCAGTGCAGAAAA[A/T]AAACCTCTGAGGAAG | 79658 |
| rs59129054 | snp | A/G | 0.0858192 | 0.188533 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147860589 | TCCATCCACACCCCT[A/G]CATTCTACTTAATAG | 79658 |
| rs59135572 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148066298 | TCACATCCCAGTATG[C/T]AGAACTGAGTCACAT | 79658 |
| rs59178803 | snp | A/G | 0.0633504 | 0.166319 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147888493 | CATTCCTACCATATA[A/G]ATACTAATATGTAAA | 79658 |
| rs59222333 | snp | A/G | 0.0908922 | 0.192833 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147886550 | ACTAGTTGAAATTTC[A/G]TAGTCACTCATCACA | 79658 |
| rs59226567 | in-del | -/TGTG | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147736154 | GTGTGTGTGTGTGTG[-/TGTG]AAGCTAAAGGGGCCC | 79658 |
| rs59228616 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147876043 | TGATTTACAGGACTT[C/G/T]CAATCCGACCTAAAA | 79658 |
| rs59246980 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147740066 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTTGC | 79658 |
| rs59333422 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147874630 | ACAGATTGATTGAGT[C/T]AGATTGGTTGTTGCA | 79658 |
| rs59346541 | snp | A/C | 0.0197687 | 0.0974348 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147811805 | TGAGCTCCGATATAA[A/C]GATGGTGATTTATTT | 79658 |
| rs59356913 | snp | C/T | 0.029116 | 0.117091 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148042364 | CAGAGTAAATTCATA[C/T]GCCTTTACATTAGAT | 79658 |
| rs59378015 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148052279 | TTCCTCAACCCCAGC[A/G]CTCCTTGAGGGCCAG | 79658 |
| rs59418577 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148051462 | AAGAAAATCTCTTTT[A/G]AGAAATATCGGGCAT | 79658 |
| rs59470864 | in-del | -/A/ATATA | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147793321 | TATATATATATATAT[-/A/ATATA]TTTTTTTTTTTTACA | 79658 |
| rs59476202 | in-del | -/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148061108 | TTCCTTTTTTTTTTT[-/T]AAAGAAAGATGTGAG | 79658 |
| rs59513990 | in-del | -/ATCTGTCT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147839142 | TCTATCTATCTATCT[-/ATCTGTCT]GTCTGTCTATGTATA | 79658 |
| rs59532898 | snp | G/T | 0.141934 | 0.225437 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147908369 | GGAAAGTCAGTTTGC[G/T]TAGCGAAAAGACTAA | 79658 |
| rs59533896 | snp | G/T | 0.14933 | 0.228835 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147853893 | AATTAATTTTGATAT[G/T]AGATGAGGTTCTCTT | 79658 |
| rs59535925 | snp | A/C | 0.269809 | 0.249214 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147800304 | ATGGAATCTCTCTAC[A/C]TGTGCCCCACGGTTT | 79658 |
| rs59590301 | in-del | -/T/TT | 0.370974 | 0.218781 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147848091 | AGTTTTTTTTTTTTT[-/T/TT]CTCTTCCTAAAAGAA | 79658 |
| rs59613700 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147951682 | GGTCTTAAACTCGTC[A/G]TCTCAAGTGATCCTC | 79658 |
| rs59630516 | snp | A/C | 0.0777841 | 0.181223 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147981313 | TAATTTTGTGGTTTA[A/C]CCAAAAGTCATTCAG | 79658 |
| rs59659659 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147762522 | TTTATTTATTTATTT[A/T]TATTTATTTATTTAT | 79658 |
| rs59663731 | in-del | -/TATATA | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147912594 | ATATATATATATATA[-/TATATA]AAATTCCTGTGTATA | 79658 |
| rs59688253 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147959050 | CTTTGTCAATCAGTA[A/G]CAATTAAAATAAATT | 79658 |
| rs59721708 | in-del | -/A | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147971115 | AAAAAAAAAAAAAAA[-/A]GAGTTCCTGGGCCAA | 79658 |
| rs59769427 | snp | C/T | 0.251859 | 0.249993 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148001913 | CCTTTATTTCTTTCT[C/T]CTGCCTGATTGCCCT | 79658 |
| rs59845678 | snp | A/G | 0.0858192 | 0.188533 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147856374 | AGCGTTACAGAAATC[A/G]CTGGAAAGGTTTGGG | 79658 |
| rs59860658 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147921144 | CAGTGGGGTAGATAG[C/T]GCAGATACAGCCGAA | 79658 |
| rs59893291 | in-del | -/GT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148036105 | TGTGTGTGTGTGTGT[-/GT]ATACTTTTCCAGTTA | 79658 |
| rs59933316 | in-del | -/TTTTTT/TTTTTTTTTTTTTTTT | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147837662 | TTTTTTTTTTTTTTT[-/TTTTTT/TTTTTTTTTTTTTTTT]AAAGCAGTAGCTTTT | 79658 |
| rs59965552 | in-del | -/A | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147739203 | AAAAAAAAAAAAAAA[-/A]GAAAAGAAAATACAT | 79658 |
| rs59966461 | snp | A/G | 0.0926964 | 0.194308 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147981415 | ATTCCATTGTGGTCT[A/G]AGAAGATGCTTGGTA | 79658 |
| rs59966813 | in-del | -/T | 0.259021 | 0.249837 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147853741 | GCTTGATTATTATGA[-/T]TTTTTTTTTATATTG | 79658 |
| rs60016652 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148013388 | CTTTTGGAGAATGAA[A/G]AGGTCCATGGCTTAT | 79658 |
| rs60032318 | snp | A/G | 0.0644693 | 0.167566 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147830445 | TTTTTGTTCCAAACT[A/G]TTAGGTTGGTACAAA | 79658 |
| rs60042554 | snp | A/G | 0.254944 | 0.249951 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147789814 | ATCTGTAAAACAGAT[A/G]GAAGTCATTAAAAAT | 79658 |
| rs60042934 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148004137 | AGGAGACTGAGGCTG[A/G]AGGAGCCCAGGAGTC | 79658 |
| rs60059737 | snp | A/G | 0.419616 | 0.183658 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147793383 | GAATACCCAGGATGT[A/G]CCAGTGAAGAAAGAA | 79658 |
| rs60060102 | in-del | -/ATATA | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147784861 | TATATTATAAATATA[-/ATATA]TTATAAAATATATAT | 79658 |
| rs60115613 | snp | G/T | 0.300421 | 0.244863 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148020546 | GAACATGCGTTTTTT[G/T]TTTTTTTTTTTATTC | 79658 |
| rs60146389 | snp | C/T | 0.0422008 | 0.138995 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147756723 | CATGGTTTTAGGCAT[C/T]CACTGGGGATCTTGG | 79658 |
| rs60201372 | snp | G/T | 0.15698 | 0.23205 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147959241 | CCAGAGTATTTTTTT[G/T]TTTGTTTTTGAAGAA | 79658 |
| rs60233014 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147915562 | TGGAGTGTTACATAC[A/C]TTGAATGGCATAAAT | 79658 |
| rs60237503 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148020557 | TTTGTTTTTTTTTTT[-/T]ATTCCTGCATTAGTG | 79658 |
| rs60280395 | snp | C/G | 0.0788843 | 0.182262 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147898913 | CTATCAGGAGAGCAG[C/G]ACGGGGGAACCACTC | 79658 |
| rs60333839 | in-del | -/A | 0.365232 | 0.22186 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147838473 | CTCTTAAAAAAAAAA[-/A]CACACACACACACAC | 79658 |
| rs60361452 | snp | C/T | 0.0988009 | 0.199095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147972361 | CCCATTGCATAAATA[C/T]ATGTAATAGTATCCC | 79658 |
| rs60374690 | snp | G/T | 0.0107246 | 0.0724382 | downstream-variant-500B | ARHGAP10 | GRCh38.p7 | 4:148072948 | GGGGCGTGTTCCTGG[G/T]GGCAGCAGCAGCCTC | 79658 |
| rs60552583 | snp | A/G | 0.117188 | 0.211804 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147951716 | CCTTGGCCTCCCAAA[A/G]CACTGGGGTTACAGG | 79658 |
| rs60635047 | snp | A/G | 0.396 | 0.202938 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147970917 | ACATGGCAAAACCCC[A/G]TCTCTACTTAAAAGA | 79658 |
| rs60642008 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148010893 | ATGACATTTTTAATA[G/T]AAAAATTGCCCCAAT | 79658 |
| rs60677226 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147813911 | TACCTCTTCTGCAAT[G/T]TAAAGTGATATAAAT | 79658 |
| rs60682964 | snp | A/G | 0.0629771 | 0.165899 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147757611 | TGCTGTAGCATTGAC[A/G]ACTTCCATCCGTTCA | 79658 |
| rs60691462 | snp | G/T | 0.0263992 | 0.111815 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147872164 | CCTCTGAGGAAGTTG[G/T]GTGGTGAGGGAGAGG | 79658 |
| rs60770463 | snp | A/G | 0.0916144 | 0.193427 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147930644 | GTTATGTAATTTCTA[A/G]CCTATCTTCTCATTT | 79658 |
| rs60865948 | in-del | -/AGAG | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147921561 | TTGGGATAATGACAG[-/AGAG]CATGTGGATGTAAGG | 79658 |
| rs60882169 | snp | A/G | 0.0726307 | 0.176182 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147965882 | TAAAAATATAAAACA[A/G]CTTCAGATGATAAAT | 79658 |
| rs60902361 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147785001 | ATATATATTATGAAA[C/T]ATATGTTATATATTA | 79658 |
| rs60979828 | in-del | -/A | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147793323 | TATATATATATATTT[-/A]TTTTTTTTTTACAAA | 79658 |
| rs60984359 | snp | A/T | 0.228547 | 0.249078 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148040994 | TGTTAATTAGAAGTA[A/T]CTAAGTTTATTCTGA | 79658 |
| rs61012783 | snp | G/T | 0.0528381 | 0.153711 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147874704 | TTTTAAACCTAAAAT[G/T]TAGTAATAGTGTGAG | 79658 |
| rs61064255 | in-del | -/ATATATATATATAT/ATATATATATATATATAT | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148043652 | TATATATATATATAT[lengthTooLong]TTTAGGTGTATAAAT | 79658 |
| rs61078731 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147969345 | TTTTTTTTTTTTTTT[-/T]GCCAGTGGTGGTGAA | 79658 |
| rs61080266 | snp | A/G | 0.208169 | 0.246476 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147979840 | CTTCTCAGCTCAGAT[A/G]TTACTGATATAAAGA | 79658 |
| rs61085580 | snp | C/T | 0.0777841 | 0.181223 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147980216 | TCTTCTTTCAATGCC[C/T]AGTTTGTTGGTTTTT | 79658 |
| rs61120930 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148001832 | AGATGATGGGGTTTT[C/T]TAAATATGCAGTCAT | 79658 |
| rs61167574 | in-del | -/A | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147910361 | CTCAAAAAAAAAAAA[-/A]TTGTACAAAATACTT | 79658 |
| rs61300612 | snp | A/G | 0.113685 | 0.209567 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147930466 | AAAACTGCCCCTGAA[A/G]CTGAAAAGATAAGAA | 79658 |
| rs61479941 | snp | C/T | 0.121717 | 0.214577 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147867587 | AAGTTGAGAGTGGGC[C/T]GGGCACAGTGGTTCA | 79658 |
| rs61613124 | in-del | -/A | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147801769 | AGGTCATCGCTGTTT[-/A]CTCCACAGACATCAG | 79658 |
| rs61659434 | snp | A/G | 0.198014 | 0.244535 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148029042 | TACGTATTCTTATGC[A/G]TAACTGCTTTGAAAA | 79658 |
| rs61688243 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147906521 | GATAAATTTTAGGTT[A/G]CATGTATTTTACCAC | 79658 |
| rs61692055 | in-del | -/GTGT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148036102 | TGTGTGTGTGTGTGT[-/GTGT]ATACTTTTCCAGTTA | 79658 |
| rs61748165 | snp | C/T | 0.00843659 | 0.0643981 | synonymous-codon, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147906644 | GTCTTTCAGGCCTGG[C/T]GTTTCCTTGACCATG | 79658 |
| rs61748167 | snp | C/T | 0.00789085 | 0.062315 | synonymous-codon, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148023382 | CAAGAGGCCCGTGGC[C/T]GTCTACAATCTTTGT | 79658 |
| rs61758693 | snp | A/C | 0.0051093 | 0.0502847 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148023409 | TTGTCTGGAGCTGGA[A/C]GATGGTAAGATGTTA | 79658 |
| rs61758694 | snp | A/G | 0.00190918 | 0.0308374 | synonymous-codon, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147881876 | GAAAGAATGTACCAA[A/G]AGGCATACTGACTCC | 79658 |
| rs62330666 | snp | A/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147755987 | CTTGACCCTGTTGGT[A/T]ATTTTTTTTTTCTGT | 79658 |
| rs62330667 | snp | A/G | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147766167 | TGGTGGTGGGTGTCT[A/G]TAGTCCCAGCTACTC | 79658 |
| rs62330668 | snp | G/T | 0.407502 | 0.194147 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147766569 | GGGTGTGTGTGGGTG[G/T]GTGTGTATATATACA | 79658 |
| rs62330669 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147766689 | CTCCAGCCTGGGCGA[C/T]AGAGCAAGACTCCAT | 79658 |
| rs62330670 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147766816 | TATATATATATATAT[A/T]TATATATATATATAT | 79658 |
| rs62330671 | snp | A/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147766820 | TATATATATATATAT[A/T]TATATATATATATAT | 79658 |
| rs62330672 | snp | A/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147766824 | TATATATATATATAT[A/T]TATATATATATATAT | 79658 |
| rs62330673 | snp | A/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147766828 | TATATATATATATAT[A/T]TATATATATATTTAT | 79658 |
| rs62330674 | snp | A/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147766832 | TATATATATATATAT[A/T]TATATATTTATTTAT | 79658 |
| rs62330675 | snp | C/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147776872 | TGCTGTGAAGAGTTT[C/T]GAGGACTTTCGTTAG | 79658 |
| rs62330676 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147783826 | AACACACATTAAATT[A/G]TGTATTATATTTATA | 79658 |
| rs62330693 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147818764 | CTTATGCTTTTGTTT[A/T]GAAAAGAAGAAGACA | 79658 |
| rs62330694 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147820150 | CTAGTAAAGATGTAG[C/G]CTCAGGGAATAGCAA | 79658 |
| rs62330695 | snp | C/T | 0.416708 | 0.186302 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147827928 | TTCCTGCCTCAGCCT[C/T]CTGAGTAGCGGGGAC | 79658 |
| rs62330696 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147836284 | TAGGCAGATATTCAG[G/T]GAATTAAATCAGAGA | 79658 |
| rs62330697 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147840805 | TTTAGCTCGAGAGCT[C/T]CTTGAACTGTGATTC | 79658 |
| rs62330698 | snp | A/C | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147852388 | CTGGGTCTGGATTCA[A/C]GTGCTCCATTCTGTG | 79658 |
| rs62330729 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147865975 | GATAAGGAAATAGAA[A/G]TAGAGAAAGGCTGAG | 79658 |
| rs62330731 | snp | A/G | 0.190833 | 0.242898 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889356 | CCAGTGTGCAGTGCA[A/G]TGGCACGATCTCGGT | 79658 |
| rs62330732 | snp | C/T | 0.466824 | 0.124448 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147897860 | CTTTTTTTGGCTATA[C/T]GTGTATATTTATTTA | 79658 |
| rs62330733 | snp | G/T | 0.415891 | 0.18703 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147898185 | CTTAGGCTGCCTTAG[G/T]CTGCATTTCTTGTAA | 79658 |
| rs62330734 | snp | C/G/T | 0.41408 | 0.188621 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147898186 | TTAGGCTGCCTTAGG[C/G/T]TGCATTTCTTGTAAT | 79658 |
| rs62330735 | snp | A/C | 0.467132 | 0.12391 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147898204 | CATTTCTTGTAATGC[A/C]GGTCTGCTAGAGAAG | 79658 |
| rs62330737 | snp | C/T | 0.47709 | 0.104548 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147899152 | ACAAGAGTTGGAGGG[C/T]GGGTTCAGACTCTCT | 79658 |
| rs62330738 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147899874 | AACTTGTTACGTGCT[G/T]GGTTTTTTTTTTTTT | 79658 |
| rs62332176 | snp | G/T | 0.430434 | 0.173042 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147904650 | TGGACATTTGGGTTG[G/T]TTCCAAGTCTTTGCT | 79658 |
| rs62332178 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911573 | TTCACCGTGTTAGCC[A/G]GGATGGTCTTGATCT | 79658 |
| rs62332179 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147923369 | ACACCTAGGTGCATG[C/T]ACTGTATGATATGCA | 79658 |
| rs62332200 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147966842 | AAACCATGAAAAGGT[A/T]AAATTTTTTTTTTCT | 79658 |
| rs62332201 | snp | A/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147999944 | TTTTTTTTTTTTTAA[A/T]TTATACTTTAGTAGG | 79658 |
| rs62332202 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148001793 | TGCTGAAGTTGCTTA[C/T]CAGCTTAAGGAGATT | 79658 |
| rs62332203 | snp | G/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148009943 | TGGTATCTGAATAAG[G/T]AACAGTTCTGTTCCT | 79658 |
| rs62332204 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148012335 | AGGTCATCCAAGAAT[C/T]TAAGCAGGAACATTT | 79658 |
| rs62332926 | snp | A/T | 0.0283406 | 0.115616 | upstream-variant-2KB | ARHGAP10 | GRCh38.p7 | 4:147731583 | GAAAGGAACCGGGAT[A/T]AGGAAAAGAGCCCCC | 79658 |
| rs62332927 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147747171 | TTTTTTTTTTTCCCC[C/T]AAAGTATTAAAACCG | 79658 |
| rs62642441 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147784207 | ATTGTGTATTATATA[A/T]TTTACATAACATTAA | 79658 |
| rs62857260 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147899877 | TTGTTACGTGCTGGG[G/T]TTTTTTTTTTTTTTC | 79658 |
| rs63684062 | snp | G/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147768756 | CTTTTTTTTTTTTTT[G/T]GGCAGGGAATCTTGC | 79658 |
| rs66465708 | in-del | -/GTCT | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147839154 | TCTATCTGTCTGTCT[-/GTCT]ATGTATATATAAAGT | 79658 |
| rs66466446 | multinucleotide-polymorphism | CT/TG | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147776115 | ATCATTTATGGCCTC[CT/TG]CGTAATCATTAACTT | 79658 |
| rs66488204 | snp | C/T | 0.263535 | 0.249633 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147826681 | TTTCTCCTGTGATCC[C/T]TACTCCCCTTGACCC | 79658 |
| rs66538210 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147868244 | TTTGTTTTTTTTTTT[-/T]GAGACAGGGTGTCAC | 79658 |
| rs66576812 | in-del | -/T | 0.444267 | 0.157354 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147811584 | CAAATATGCAATGGC[-/T]TTTTTTAAAAAAAAA | 79658 |
| rs67176657 | in-del | -/T | 0.0322114 | 0.122752 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148038910 | TTTTTAAAATGACAG[-/T]TTTTTTTGTTTCTAA | 79658 |
| rs67269531 | in-del | -/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147788139 | AAAAAATTTGATTTT[-/G]TTTTTTTTAAAAAGC | 79658 |
| rs67509221 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147919568 | ATCTTTTAAAAACAA[-/T]TTTTTTTTCTTTTTT | 79658 |
| rs67614445 | in-del | -/G | 0.375 | 0.216506 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148020546 | GAACATGCGTTTTTT[-/G]TTTTTTTTTTTATTC | 79658 |
| rs67845807 | in-del | -/A | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147833912 | GGCACCTCTCAGATA[-/A]GAGGAAGGAGGAGTG | 79658 |
| rs67852364 | in-del | -/ACACACACACACACACACACACACAC | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147873723 | CACACACACACACAC[-/ACACACACACACACACACACACACAC]TCTTAGCCTGGTGTG | 79658 |
| rs67913037 | snp | C/G | 0.335559 | 0.234904 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147925524 | TCCCATCCTTTCCAG[C/G]TTACTTTAATACTTA | 79658 |
| rs68077800 | in-del | -/TCT | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889668 | TGTAAACATACTTTG[-/TCT]TCTTTACAAGTATCT | 79658 |
| rs70958581 | in-del | -/T | 0.49907 | 0.0215454 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147745790 | CTTTTTTTTTTTTTT[-/T]GAGATGGAGTTTCGC | 79658 |
| rs70958582 | in-del | -/ACTTTT | 0.450734 | 0.149016 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147748995 | CCTATACATAAGATA[-/ACTTTT]ACTTTTGAAACTCAC | 79658 |
| rs70958583 | in-del | -/ATATATATATATATATATATTTAT | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147766820 | TATATATATATATAT[-/ATATATATATATATATATATTTAT]TTATTTATTTATTTA | 79658 |
| rs70958585 | in-del | -/AT/ATA | 0.434976 | 0.168179 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147784831 | ATATATATTATAAAT[-/AT/ATA]ATATATTATAAAATA | 79658 |
| rs70958586 | in-del | -/CTCTCTCTCTCTCTCTCTCTCTCTATATATATAT | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147798759 | TCTCTCTCTCTCTCT[lengthTooLong]ATATATATATATATA | 79658 |
| rs70958587 | in-del | -/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147829056 | GCTAATTTTTTTGTA[-/T]TTTTTTTTTTTTTGA | 79658 |
| rs70958588 | in-del | -/AAAAAAAAA | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147832664 | AAAAAAAAAAAAAAA[-/AAAAAAAAA]GGAAATTGGAGCTCA | 79658 |
| rs70958589 | in-del | -/A | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147838474 | AGACCCTTGTCTCTT[-/A]AAAAAAAAACACACA | 79658 |
| rs70958590 | in-del | -/A | 0.330249 | 0.23677 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147865580 | CATGTGGATTTCAGC[-/A]AAAAAACACTGGATC | 79658 |
| rs70958591 | in-del | -/GT | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147870974 | TGTGTGTGTGTGTGT[-/GT]TTGAGATGGAGTCTT | 79658 |
| rs70958592 | in-del | -/A | 0.375 | 0.216506 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147887442 | TATTTCATTCATCTT[-/A]AAAAAAACAAAAGCC | 79658 |
| rs70958593 | in-del | -/A | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147895535 | AAAAAAAAAAAAAAA[-/A]TTAGCCAGGTATGGT | 79658 |
| rs70958594 | in-del | -/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147912670 | TTTTTTTTTTTTTTT[-/T]GGGGAGACAGGGTAT | 79658 |
| rs70958598 | in-del | -/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147936318 | TTTTTTTTTTTTTTT[-/T]GAGACGGAGTCTTGC | 79658 |
| rs70958599 | in-del | -/T | 0.4944 | 0.0526182 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147982366 | TCTTTTCTTTCTTTC[-/T]TTTTTTTTTTTTTTT | 79658 |
| rs70958602 | in-del | -/TTTTTTTTT | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148039397 | TTTTTTTTTTTTTTT[-/TTTTTTTTT]GAGATAGAGTCTCAC | 79658 |
| rs70962703 | in-del | -/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148050391 | TTTTTTTTTTTTTTT[-/T]AAGATGTAGTCTCGC | 79658 |
| rs70962704 | in-del | -/AG/GA | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148059974 | GAGAGAGAGAGAGAG[-/AG/GA]GGGAGAGAGAGGAGA | 79658 |
| rs71250029 | in-del | -/G | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147837650 | TTTTTTTTTTTTTTT[-/G]TTTTTTTTTTTTAAA | 79658 |
| rs71593789 | multinucleotide-polymorphism | CGT/TGC | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147832082 | TCCCCCTGACTGCCC[CGT/TGC]CCGACATACACACAC | 79658 |
| rs71593790 | in-del | -/TTTTTTTTTT | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147837644 | AATCTCTGGTCACTG[-/TTTTTTTTTT]TTTTTTTTTTTTTTT | 79658 |
| rs71593791 | in-del | ATATA/GAG | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148017676 | TATATATATATATAT[ATATA/GAG]TATGTGTGTGTATGT | 79658 |
| rs71594235 | in-del | -/C | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147757157 | TTGGATATCAGAACC[-/C]TGAAAGTTAATGGGA | 79658 |
| rs71594240 | in-del | -/T | 0.267334 | 0.249398 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147853741 | TATGATTTTTTTTTT[-/T]ATATTGGCAAGTTCT | 79658 |
| rs71594244 | in-del | -/CAA | 0.389903 | 0.207189 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147900819 | GTCTATAAATAAATT[-/CAA]CAACAACAACAGCAA | 79658 |
| rs71594247 | in-del | -/A | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147983141 | CCGCCTTGGCCTCCC[-/A]AAAGTGCTGGGACTA | 79658 |
| rs71594248 | in-del | -/C | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147983166 | GACTACAGGCATGAG[-/C]CCATGGTGCCTGGCT | 79658 |
| rs71594250 | in-del | -/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148052392 | TTTTTGCACATTTGC[-/T]TTTTTTTTTTTTTTT | 79658 |
| rs71616568 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147783634 | AGAACACATTAAATT[A/G]TGTATTGTATAATTT | 79658 |
| rs71616569 | snp | A/C | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147798795 | TCTCTCTCTCTCTAT[A/C]TATATATATATATAT | 79658 |
| rs71616570 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147856430 | AATCTTATTGCTATA[C/T]AGGTTGATCATCCTG | 79658 |
| rs71616571 | snp | C/T | 0.0614824 | 0.164198 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147860420 | GCACTCCAGCCTGGG[C/T]GACAGCTCCGTCTCA | 79658 |
| rs71616573 | snp | A/C | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147945090 | GGGCCAGGTTGTTAG[A/C]GGCGTGTAAGCCCAG | 79658 |
| rs71616574 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147964210 | TACGCTACAGGCTGT[A/G]CTCTCCTGCCCTTGT | 79658 |
| rs71616575 | snp | G/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148028921 | AGGTAAATCTATCAT[G/T]GTGTTTATGTTTTTG | 79658 |
| rs71616576 | snp | C/T | 0.171704 | 0.237423 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148048305 | ATGATTGTGAACTTA[C/T]TAAGTATTAAGAGAG | 79658 |
| rs71616577 | snp | G/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148054682 | CCTAGCCTCTTGCTT[G/T]GGGGATCTGCTTTGT | 79658 |
| rs71640642 | multinucleotide-polymorphism | AA/GG | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147873888 | TTTAAAAAAAAAAAA[AA/GG]GGGGGGATAAGAAAA | 79658 |
| rs71686498 | in-del | -/TCTG | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147839143 | CTATCTATCTATCTA[-/TCTG]TCTGTCTGTCTATGT | 79658 |
| rs71889384 | in-del | -/ATATATATATATATATATATATAT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148043615 | GAGACCCTCTCTCTA[-/ATATATATATATATATATATATAT]ATATATATATATATT | 79658 |
| rs71892750 | in-del | -/ACAAC | 0.336474 | 0.234568 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147920123 | AACGTCTTTTAAAAA[-/ACAAC]ATAACCTCGCTGGGC | 79658 |
| rs71973085 | in-del | -/T | 0.424037 | 0.179474 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147767368 | GCTGCAGAATTTATC[-/T]TTTTTTTTTTTTAAT | 79658 |
| rs72024363 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148052393 | TTTTGCACATTTGCT[-/T]TTTTTTTTTTTTTTT | 79658 |
| rs72123695 | in-del | -/CC/CTAAGCC/TAAGCC | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148003894 | TCTTTTATCTGAGTG[-/CC/CTAAGCC/TAAGCC]TAAGCCTAAATCAGC | 79658 |
| rs72246174 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147765339 | TGTGTGTGTGTGTGG[-/T]GGGGGGGGGTGTGAG | 79658 |
| rs72393784 | in-del | -/TCTC | 0.0607341 | 0.163335 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148005735 | AATTCTTATGTCCTT[-/TCTC]TTTCATGATTGAGGT | 79658 |
| rs72399544 | in-del | -/ATTAA | 0.319376 | 0.240181 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147783177 | TAATTTATATAACAC[-/ATTAA]ATTATATATTGTATA | 79658 |
| rs72470150 | in-del | -/CT | 0.0178098 | 0.0926698 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148013861 | CATTTAAGGAAGACT[-/CT]TTTTTATCAGGGTTC | 79658 |
| rs72522237 | in-del | -/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147983073 | TTTTAGTGGAGATGG[-/G]GTTTCACCATGTTGG | 79658 |
| rs72527110 | in-del | -/A | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147924746 | CCTTATTAACTCTGC[-/A]CWKTAACCTCTCTGT | 79658 |
| rs72617450 | snp | A/G | 0.409382 | 0.192607 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147937601 | CTGTTATACACACAC[A/G]TGCACATGTATATTC | 79658 |
| rs72617451 | snp | A/G | 0.155987 | 0.23165 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147995433 | TGATCTACTTACAGT[A/G]TGGAGTGTGGGAGGA | 79658 |
| rs72619778 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148036490 | ATAGTGAGTTCTCAC[A/T]AGATCTGATGGTTTT | 79658 |
| rs72724333 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147812217 | GCATTTCTAAAAGGC[C/T]GCGTAGGAAGTGGGG | 79658 |
| rs72724335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147813105 | GTACTGCCTGTTGCA[A/G]TTTTTTACATGGATT | 79658 |
| rs72724337 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147825790 | ATTTTTTTTCTTAAC[C/G]CTCTTTGATAGTTGT | 79658 |
| rs72724339 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147827660 | GAAAGACTCTTGTTT[C/T]ACTTAAATTTTTTTT | 79658 |
| rs72724342 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147849773 | TTTTGAAAAGCCCCC[A/G]GGTATTGTCTACTGT | 79658 |
| rs72724348 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147860961 | TTCTTGTAAGTGAGG[A/G]CTGTTGTCACGGAAT | 79658 |
| rs72724349 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147862246 | TGGGTGGCAACAGTA[C/T]CTGGGCTTGGCTACA | 79658 |
| rs72724356 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147891022 | AAAATCCTCATACAC[C/T]GAGAGTGAGAATTTA | 79658 |
| rs72724361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147903064 | TCCAACTTTGGGAAT[C/T]GTAAATGCTACATGA | 79658 |
| rs72724371 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147920845 | GAAAGTATATTTTGG[C/T]GTTTAGAGGAAACTC | 79658 |
| rs72724377 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147942243 | TTGTCTTTGTAGAAA[G/T]GGGAAATAATTTAAT | 79658 |
| rs72724386 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147972508 | AACTGAGATTGACCC[C/T]CAAAGCCTTTGCTTT | 79658 |
| rs72724389 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147975066 | ATAGCCTTTATGTAT[C/T]ACAGTTTTTGTGGAT | 79658 |
| rs72724393 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147984371 | GTCCGCCACAGCACA[C/T]TGAGGAGGCGGGAAG | 79658 |
| rs72724397 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148004568 | TTGGAAGTAATCAAC[C/T]ACGTGAACTGTCTGT | 79658 |
| rs72724400 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148008849 | GATATTAAGACATTG[A/G]ATTAAAACATTGAAT | 79658 |
| rs72724402 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148017182 | AGAAACCCAGCAATG[C/G]CTGACTGTTCAGATT | 79658 |
| rs72726605 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148052035 | GATACCAGAGTACCC[C/T]GCTCCCCCAAATATG | 79658 |
| rs72726618 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148063460 | CCTTGTATCAGGGCC[C/G]TGCCTCACCCAGTTC | 79658 |
| rs72951429 | snp | G/T | 0.00953873 | 0.0683987 | upstream-variant-2KB | ARHGAP10 | GRCh38.p7 | 4:147730612 | ACAAAAGGGCTTATT[G/T]AGTAGGAGGCTTATT | 79658 |
| rs72951430 | snp | A/C | 0.185788 | 0.241613 | upstream-variant-2KB | ARHGAP10 | GRCh38.p7 | 4:147731243 | TTTCATAACACACAA[A/C]ATAGGCTTTTTGAGG | 79658 |
| rs72953456 | snp | C/T | 0.121369 | 0.214369 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147737446 | AGGTGTCAGCCACTG[C/T]GCCTGGCCTTAATGG | 79658 |
| rs72953462 | snp | A/G | 0.128288 | 0.218372 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147744115 | AGCAATTACATTCAC[A/G]TTGTTGAATCAGTAT | 79658 |
| rs72953473 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147754084 | TCTGTCTTTCGTCCT[C/T]CAGCAGTGTCTAGAA | 79658 |
| rs72953475 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147755277 | TTAAATTTTCTCTTA[C/T]ATAACCAGTCTTTTG | 79658 |
| rs72953477 | snp | C/T | 0.0562307 | 0.157967 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147756224 | TAATACCTCATGGGC[C/T]GCAGTTCTTAATTGC | 79658 |
| rs72953481 | snp | C/T | 0.0554779 | 0.157039 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147757813 | GTCAGGCCTGGCTCA[C/T]GCTGGTCATTGGCCA | 79658 |
| rs72953485 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147758409 | TAAAATGTATAATCA[A/G]TGGCTTTTAGTGTAG | 79658 |
| rs72953487 | snp | C/G | 0.0696718 | 0.173152 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147758478 | AACATATTCATCACC[C/G]CAGAAAGAAAGCCTG | 79658 |
| rs72953492 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147763088 | TGTATAAGATTTATT[A/G]CAAGATGGCTACTAA | 79658 |
| rs72953495 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147767820 | AAAATTGAAAATAAT[C/T]GTGATGGCAGTGGAG | 79658 |
| rs72953496 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147768522 | AAAAAAGTAATTAAA[A/G]GTTGAGATTTAATGA | 79658 |
| rs72953498 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147769329 | GAAGAAGGAAAAATG[A/G]AGGTATCCATCCATA | 79658 |
| rs72953501 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147773621 | TGTTGCCATGATGTC[A/G]TAAGGATTTAAAAAC | 79658 |
| rs72953502 | snp | C/G/T | 0.0547245 | 0.156101 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147774374 | AATTTATTTCTGCAG[C/G/T]TATCCAATGTTGTTG | 79658 |
| rs72955506 | snp | A/G | 0.0584853 | 0.160693 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147777627 | ACCTTCCTGTCAGAC[A/G]GTCAGATCTCTTAAC | 79658 |
| rs72955514 | snp | C/T | 0.0341408 | 0.126114 | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147781234 | CTGTAGTCCCAGCTA[C/T]TCAAGAGGCTGAGGC | 79658 |
| rs72955517 | snp | A/G | 0.163892 | 0.234703 | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147782407 | TACATTTTCAGGAGT[A/G]GGTTCTTCCGGTATG | 79658 |
| rs72955519 | snp | A/G | 0.0333695 | 0.124785 | intron-variant, nc-transcript-variant | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147782619 | ATCTAAATGCAGCAT[A/G]CCAGTCCTGAGATGC | 79658 |
| rs72955524 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147786220 | AGAGCCTGGAAGCCT[C/T]TCTTAAGCAGCTGCA | 79658 |
| rs72955525 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147787250 | TTTATTTATTTATTT[A/T]TTCTTTTCCTTGGGA | 79658 |
| rs72955541 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147796580 | CCATGGCTGGAATGC[A/C]GTGGTGTCATCTCGG | 79658 |
| rs72955545 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147802759 | CTGTCAAAATTCAGA[A/G]CAGATGTTGTGACTT | 79658 |
| rs72955555 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147815756 | CTGTAGTCCCAGCTA[C/T]TCAAGAGGTTGAGGT | 79658 |
| rs72955557 | snp | G/T | 0.0197687 | 0.0974348 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147815932 | CTCCAAAAACTGTTA[G/T]ATAATAAGTTAGCGT | 79658 |
| rs72955571 | snp | C/T | 0.046775 | 0.145601 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147821273 | TGGCTACAAGACTAG[C/T]CCAGGTTCAAGGGGT | 79658 |
| rs72955575 | snp | G/T | 0.0391387 | 0.134304 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147824981 | CACATTACCTTGCCC[G/T]AGATCACATGGCATC | 79658 |
| rs72955587 | snp | C/T | 0.039522 | 0.134904 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147834633 | AGACTTACCCCAGAA[C/T]GGCACTGCAGCCTCA | 79658 |
| rs72955600 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147851714 | GCATAGTATTAGAGG[C/T]CCTGAGATACAACTA | 79658 |
| rs72957722 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147865342 | ACAATCGTTTGTAAC[A/G]TGACTTCAAACACAA | 79658 |
| rs72957723 | snp | G/T | 0.124491 | 0.216211 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147865755 | GATTAAAAATGAGCA[G/T]TTGTGGAGCTATGGT | 79658 |
| rs72957736 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147872453 | ATAGGTAGATAAAGA[A/G]GTAGTGATTGTGTGT | 79658 |
| rs72957750 | snp | A/G | 0.0501905 | 0.150254 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147877517 | AGGTGTAGAAACTTT[A/G]TTTGTTTGTACATGA | 79658 |
| rs72957758 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147882591 | GTAGCTAGCTACTAA[C/T]ACAGAACAACATTCA | 79658 |
| rs72957761 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147883718 | CTTTTTTTTTGAGAC[A/G]AGTCTCACTTTTTTT | 79658 |
| rs72957764 | snp | A/G | 0.0825414 | 0.185628 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147884897 | CAGTGAGTGACAATT[A/G]TATTTGTATTTCTCA | 79658 |
| rs72957767 | snp | C/T | 0.121717 | 0.214577 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147886132 | TCCATTCCCAAGATA[C/T]CTCATTTCGTATGTG | 79658 |
| rs72957775 | snp | A/T | 0.0178098 | 0.0926698 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147890381 | TTTTTCTTAGCTAAG[A/T]GACACCATTTAAGAC | 79658 |
| rs72957780 | snp | C/T | 0.0670745 | 0.170406 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147892222 | TATCTGAAGCACTGG[C/T]GTTTTACAGTGATTT | 79658 |
| rs72957786 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147896404 | ATATTCAGATTTTCT[A/G]TTTTTCTTGGGTTTT | 79658 |
| rs72957792 | snp | C/G | 0.0825414 | 0.185628 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147899365 | TCTGTGTCTGTGTGT[C/G]TTTGTCTTCTGTCCA | 79658 |
| rs72957793 | snp | C/T | 0.0629771 | 0.165899 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147899427 | TCATTAGGTCTTTTT[C/T]ACATCTTTGCTCTTA | 79658 |
| rs72957795 | snp | A/G | 0.0825414 | 0.185628 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147901133 | TTTGAAATGTGTCCA[A/G]TGTTTCTCAAAGTCT | 79658 |
| rs72959712 | snp | G/T | 0.0821764 | 0.185298 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147910492 | TTATATCGAGGCCCT[G/T]TTTCCTAGCCTTGAT | 79658 |
| rs72959724 | snp | A/C/T | 0.0115144 | 0.0749975 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147918036 | TTTATAATCTTACTG[A/C/T]TTCTACAACATATGT | 79658 |
| rs72959726 | snp | C/G | 0.284209 | 0.247648 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147918594 | GGTGGGTCACATTGT[C/G]TTTCTGTTGGCCATC | 79658 |
| rs72959736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147934498 | TCCTCTATCCGTTAA[C/T]GCTTTTGATTTTGGG | 79658 |
| rs72959753 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147957671 | TGTTCTGTGGTGATG[A/G]GATAGTTTCTTCTCT | 79658 |
| rs72959754 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147965329 | CTTAACATCTCTGCC[A/G]GCAACTCAGGGTTTG | 79658 |
| rs72959758 | snp | A/G | 0.0759472 | 0.179459 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148010708 | CATGACTCTAATTGT[A/G]GCCCGTAGTCCAACA | 79658 |
| rs72959761 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148042516 | GTTTTGATACTTTCT[C/T]GACCAGAGGCTTTTT | 79658 |
| rs73853711 | snp | C/T | 0.132751 | 0.2208 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148049050 | TACATCTATGTTTCT[C/T]TGAAGTATATACTAA | 79658 |
| rs73853714 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148055902 | CAGTGAAGATGGAGG[A/G]GATTCTCCATCCGAA | 79658 |
| rs73853716 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148064348 | TTGGGGAAGGGGGGT[G/T]GGGGGGTGAAGTTTC | 79658 |
| rs73853717 | snp | C/T | 0.00552256 | 0.0522569 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148064545 | TCTGTTAATCCTGTC[C/T]GCAGGATTAATAAGT | 79658 |
| rs73853718 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148064890 | GCTTCGGGTTTACCA[A/C]CTCTGAGTCAACAGA | 79658 |
| rs73853720 | snp | A/G | 0.0115144 | 0.0749975 | utr-variant-3-prime, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148072228 | GTCAGCCCTGGGGGT[A/G]GGGGGTGGTGGGCAG | 79658 |
| rs73853980 | snp | G/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147765339 | GTGTGTGTGTGTGTG[G/T]GGGGGGGGGTGTGAG | 79658 |
| rs73853983 | snp | C/T | 0.132409 | 0.220618 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147818963 | AAAGGGGAAAATGAG[C/T]GATAGAAATGCTTAT | 79658 |
| rs73853986 | snp | A/G | 0.108048 | 0.20579 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147870556 | TGTATTGTAAAAGTG[A/G]CTAGACTTTTTTTTT | 79658 |
| rs73853987 | snp | A/G | 0.0792508 | 0.182605 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147880370 | TAAAAACACATTTAT[A/G]TAATAATGAAACAGA | 79658 |
| rs73853989 | snp | G/T | 0.142947 | 0.22592 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147903161 | CAGTCTGCCTCCACA[G/T]CTTTCTGTTGTGCCA | 79658 |
| rs73853990 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147924698 | GAAGAACATTAGCCC[A/C]AAAGACTATCTTGAT | 79658 |
| rs73853992 | snp | A/G | 0.0955749 | 0.196603 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147970742 | TGTTTTTATAAATCT[A/G]TGTATACTTTATAGG | 79658 |
| rs73853995 | snp | C/T | 0.093417 | 0.194889 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147986462 | TACTTGTTTGCTTTT[C/T]GAGAAAATCAAGGGG | 79658 |
| rs73853997 | snp | A/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147991161 | AAAAAAAAAAAAAAA[A/T]AAATAAAAGAAAACA | 79658 |
| rs73853998 | snp | A/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147991165 | AAAAAAAAAAATAAA[A/T]AAAAGAAAACAAATA | 79658 |
| rs73853999 | snp | G/T | 0.196771 | 0.244268 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147991398 | CCAAATCCACATCCC[G/T]GCTTCCTCATGTTTT | 79658 |
| rs73854000 | snp | A/G | 0.253824 | 0.249971 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147991682 | CCCTAACCATTTAGG[A/G]AATGTTTTATATCAG | 79658 |
| rs73857327 | snp | G/T | 0.0260105 | 0.111035 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148026692 | TAAATCTTTGTGAGA[G/T]TCTCATCTTTTATTT | 79658 |
| rs73857329 | snp | A/G | 0.202343 | 0.245416 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148027696 | TTAGAACTTTGAATA[A/G]TTAGCTAAAATTTAA | 79658 |
| rs74288686 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147868236 | CTAATGTTGTTGAGT[A/T]TTTTTTGTTTTTTTT | 79658 |
| rs74288690 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147933223 | GTTCTTTTAAAAATT[A/G]TTTATTTTTTTAGGG | 79658 |
| rs74318231 | snp | C/G | 0.0402882 | 0.136092 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148016280 | AGGCTGGGGTGGGAG[C/G]GTCACTTGAGACCAG | 79658 |
| rs74320883 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147776899 | TTAGGACGATAGTAC[C/T]ATGGTAAAAGCTTTG | 79658 |
| rs74331713 | snp | G/T | 0.0799831 | 0.183287 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147998826 | AATATATCTTAAAAT[G/T]TGTATTTTAGCCCTT | 79658 |
| rs74333812 | snp | C/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147814292 | TTGCTAGGATGCATC[C/T]TTTTTTTTTTTTCCA | 79658 |
| rs74341385 | snp | A/T | 0.0189856 | 0.0955633 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147929415 | CACATTTTTGACAGA[A/T]TGTTATAATGTTATG | 79658 |
| rs74356019 | snp | C/G | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147879711 | CCCCCAGCCCCCTCA[C/G]AGACCCCAGTGTGTG | 79658 |
| rs74358332 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889519 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTCA | 79658 |
| rs74409420 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147809933 | TTTTCCAAAAGATAC[C/G]TAACTTTACTTTGTT | 79658 |
| rs74417823 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147771552 | CTAGGTGGCACAATT[G/T]TTTTGTACCCATTCA | 79658 |
| rs74422252 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147794988 | TGCTTTTGCAGTTGA[C/T]TATAGTCAGTTCCAT | 79658 |
| rs74430061 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147788148 | TGATTTTTTTTTTTT[A/T]AAAAGCGTTTCTGAA | 79658 |
| rs74445292 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147758278 | CAAAAAAAAAAAAAA[A/G]GATTTTGATGTAGTT | 79658 |
| rs74473706 | in-del | -/GCC | 0.00795532 | 0.062565 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147761872 | TGAATTAAATGAGTA[-/GCC]ACTTGCTTTGGACTT | 79658 |
| rs74490287 | snp | G/T | 0.0667028 | 0.170006 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147857231 | TGTTATTTTTCTTAC[G/T]TATTTTGTTTCATTC | 79658 |
| rs74491927 | snp | A/G | 0.29175 | 0.246489 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147972352 | CATAAAATTCCCATT[A/G]CATAAATATATGTAA | 79658 |
| rs74507810 | snp | A/T | 0.242201 | 0.249878 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147972994 | TCCTGATCTCAAGTG[A/T]TCCACCGGCCTTGGT | 79658 |
| rs74509096 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147808779 | GCCCCCTCTGGTTCT[A/G]CACTCTTCTAGGACC | 79658 |
| rs74516285 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147985690 | AAGAATGACTGCCTT[G/T]TTTGAGCCTGGATTA | 79658 |
| rs74523651 | snp | A/G | 0.00117314 | 0.0241907 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148047050 | GACTGGGCATCCACT[A/G]TGTAAGTAACCGTGC | 79658 |
| rs74544408 | snp | C/T | 0.093777 | 0.195178 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147984941 | CACCTACAGGTCCCC[C/T]AATGGCAGGTCCGAG | 79658 |
| rs74546383 | snp | A/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148048960 | GCCTGGAAAGGAGAT[A/T]TTTTTTTTTTTTTTA | 79658 |
| rs74555562 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147969319 | TGTGAGAAGTTTTGT[C/T]TTGCCTTTTTTTTTT | 79658 |
| rs74559306 | in-del | -/A | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147784938 | ATATATGTTATAAAA[-/A]TATAAAACATGTTAT | 79658 |
| rs74565140 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147924990 | TTTTTTTTTTAAAAT[A/G]GCAATTTACATTGGG | 79658 |
| rs74596313 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148064383 | TGTTTTCCACATTTT[A/C]ATTGGTGTCTTTTGT | 79658 |
| rs74597103 | snp | A/C/T | 0.0225045 | 0.103662 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148006448 | GCCTGACCCCAGCAG[A/C/T]GTCTGATCATTGTTG | 79658 |
| rs74599272 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147756763 | TCCCTGGATAAGGGG[A/G]GACCACTATATTGTT | 79658 |
| rs74599503 | snp | G/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147768513 | AATTAAAAAAAAAAA[G/T]TAATTAAAGGTTGAG | 79658 |
| rs74608924 | snp | A/T | 0.0352966 | 0.128072 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147833742 | AAGATTAGCAGGATT[A/T]TTTTGTGGTAGGATA | 79658 |
| rs74623914 | snp | C/T | 0.0670745 | 0.170406 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147847923 | AGAAATAATTTCCAC[C/T]GGTCTTTCCTGAATT | 79658 |
| rs74628945 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889460 | ATACACCGCCACGCC[C/T]GGCTAATTTTTGTAT | 79658 |
| rs74665904 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147739238 | AAATCAGAGCTCAGT[A/G]GTATCTTGGGAAAAT | 79658 |
| rs74670711 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147775103 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 79658 |
| rs74673387 | snp | A/G | 0.154661 | 0.231107 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147959697 | ACAAAGGACATGAAC[A/G]CATCCTTTTTAATGG | 79658 |
| rs74706893 | snp | A/C | 0.0444908 | 0.142359 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147900654 | AGCTGAACCAGTAGA[A/C]TGCATTGCAGCAATA | 79658 |
| rs74729351 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147883035 | AATGCTGCTTCCTCT[C/T]TTAGATGATATAGTT | 79658 |
| rs74771124 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147853942 | GTCATGCCAGCACCA[A/G]TGGTTGAATCGTCTC | 79658 |
| rs74774738 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147791998 | CATGTCTCCTGACGC[A/G]TGTATGATGTGTATG | 79658 |
| rs74788103 | snp | A/G | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147785099 | AAAAAAAAAAAAAAA[A/G]AGAATAACATCTAAG | 79658 |
| rs74790012 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147775861 | TAGAATGCTTACTAT[A/G]TACCAGATATTGTCA | 79658 |
| rs74837872 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147767540 | AAGAAGACTGAGCCT[A/G]TATTAAAAGATTATC | 79658 |
| rs74865824 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147964197 | CTCTGCGGGCCCTTA[C/T]GCTACAGGCTGTACT | 79658 |
| rs74866651 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147861740 | GGTCATCCTGACTAG[A/T]GGAGGAGACCCCCAG | 79658 |
| rs74871968 | snp | A/G | 0.105214 | 0.203807 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148062317 | CTCGGGAAACTGCTC[A/G]TGGAAACTGGTGTAC | 79658 |
| rs74880402 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147961799 | CTCTCCTTACCTCTC[A/G]AGTCCACTGGCTGTG | 79658 |
| rs74905184 | snp | A/C | 0.0696718 | 0.173152 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147995134 | ATTATTGAGATAGAT[A/C]CAAACTGTTATAAAT | 79658 |
| rs74908388 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147788139 | TAAAAAATTTGATTT[G/T]TTTTTTTTAAAAAGC | 79658 |
| rs74978856 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147970220 | AACTTCATATGGATG[C/T]GTGGATCTATGTTAG | 79658 |
| rs74979568 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147772911 | AGTTTGAGTCATTGG[A/G]TGGGCGGAACTGATT | 79658 |
| rs75019253 | snp | A/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147910677 | CTCTGTACCCTTGAT[A/T]TTTTTTTTTAACTTA | 79658 |
| rs75027476 | snp | C/T | 0.021333 | 0.101051 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147795256 | CTATGCCCATTTGAG[C/T]TTTGATATGTAATCT | 79658 |
| rs75036872 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148044301 | AACCCCTGGTCTCCA[G/T]TTCCCCAAAGTTGCT | 79658 |
| rs75076449 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147828557 | ATTTCCAACATGCTT[C/T]GTGGTAATCAAGTGA | 79658 |
| rs75093101 | snp | C/G | 0.0785177 | 0.181917 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147986759 | CATGATTCAGATCCT[C/G]CTCAACAACTCTGAA | 79658 |
| rs75096424 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148012978 | TTGTGTTTGCCAACA[C/T]TTCTACAAGGAATAT | 79658 |
| rs75111636 | snp | A/C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148045412 | CTAGCTTAATCAGAG[A/C/T]CTGGAATTTCTCTTA | 79658 |
| rs75181114 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148035081 | GGTTCCTGGAGTTGT[A/G]ACCTGATGCCTATTA | 79658 |
| rs75193717 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147900846 | ACAACAACAACAACA[C/T]GCCTTGAGACAGGTT | 79658 |
| rs75218969 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147841868 | TTTGCCACAACTACT[A/G]CTATCCTTGTTTTGG | 79658 |
| rs75220338 | snp | A/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147858344 | TCCCACAAAATTGTA[A/T]TTTTTTTTCTTGTTT | 79658 |
| rs75224309 | in-del | -/TTTT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148060363 | TTTTTTTTTTTTTTT[-/TTTT]GGCCTTCCAAAAAAT | 79658 |
| rs75236996 | snp | A/T | 0.0633504 | 0.166319 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147836194 | GTTCGTAGAAGATAG[A/T]TACTAAGAGAATCGT | 79658 |
| rs75243581 | snp | C/G | 0.0611083 | 0.163768 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147890168 | GCTTCTAAATCCTAA[C/G]GTTGGGAAATTGCTG | 79658 |
| rs75244583 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147929880 | GTTTGTTGTATAACC[C/T]ATAGAGAAATCTGTC | 79658 |
| rs75244672 | snp | A/G | 0.129664 | 0.219133 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147987274 | ACTGTTGAAGCTTCT[A/G]TAATCATATAGCCAT | 79658 |
| rs75261200 | snp | A/C | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147959525 | CTCCCCGCTCCCCCC[A/C]CCCCACGACAGGCCC | 79658 |
| rs75319180 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147863639 | TGGTAATACTATTTT[C/T]CATTTGAGGGAAAAA | 79658 |
| rs75336104 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148024326 | ATCTTTCATTTATTA[A/T]CCTTGAGCTACCCAG | 79658 |
| rs75350560 | snp | A/G | 0.0926964 | 0.194308 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147967686 | TACTCTTACGATACA[A/G]CAGAAGAGTCTGGTA | 79658 |
| rs75386394 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147877612 | TTGTCAACTTCTGCT[A/G]GGCCTAACCTTTAAT | 79658 |
| rs75391232 | snp | A/G | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911995 | TTTAAGAACATTCAC[A/G]TGTGTGTGTGTGTGT | 79658 |
| rs75400218 | snp | G/T | 0.277778 | 0.248452 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147960096 | TGTGAATTGAAATTG[G/T]TATATTGTTTTTATT | 79658 |
| rs75418649 | snp | A/G | 0.0554779 | 0.157039 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147775742 | CTCCCTAGGCATGGG[A/G]GCTCTAAATCCTTTT | 79658 |
| rs75430723 | snp | A/C | 0.0189856 | 0.0955633 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147944859 | CATTTCCTGCCTCCT[A/C]CCTTTGGGTAGGTAC | 79658 |
| rs75468729 | snp | A/C | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147755082 | AGTGAAACTCCGTCT[A/C]AAAAAAAAAAAAAAA | 79658 |
| rs75476371 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147875682 | AGTCTGAGATAGCTG[G/T]TTCTTACTAAAATCA | 79658 |
| rs75492156 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147955483 | CAGTTTGTGTTAAAA[A/G]TAGAAATCGCTTTAA | 79658 |
| rs75523766 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147994088 | AAGGGATTTCGGGCA[A/G]CTAAGCCACACAGTT | 79658 |
| rs75533512 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147818155 | CTATTTTTTTTTCTT[C/T]TTCTTTTTCTTTTTT | 79658 |
| rs75534650 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147818164 | TTTCTTCTTCTTTTT[C/T]TTTTTTTTTTTTTTA | 79658 |
| rs75550010 | snp | C/G | 0.0700422 | 0.173537 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147928251 | GGTTTAGACCCAGAA[C/G]TGAGTATTTGCTTTG | 79658 |
| rs75559966 | snp | C/T | 0.089084 | 0.191327 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147843835 | CCTTTCTTCTTTTAT[C/T]CAACACCTTGGTAGC | 79658 |
| rs75563088 | snp | A/C | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147983078 | CTAGAGATGGGGTTT[A/C]ACCATGTTGCCTAGG | 79658 |
| rs75582832 | snp | A/C | 0.0283406 | 0.115616 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147793784 | CTGTGTACGTGCCTT[A/C]CCCCTTAACAGTAAG | 79658 |
| rs75588995 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147794817 | TTAGTGTTTTTTGAA[A/G]CATGATTTTAATGTT | 79658 |
| rs75591083 | snp | A/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147959233 | TAAAAAGCCCAGAGT[A/T]TTTTTTTTTTTGTTT | 79658 |
| rs75595958 | snp | A/G | 0.0876345 | 0.190099 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148066156 | TCTTGTTTCCCTGGC[A/G]GGAGCGAGATGACTA | 79658 |
| rs75629264 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147747166 | CATCTTTTTTTTTTT[C/T]CCCCCAAAGTATTAA | 79658 |
| rs75643193 | snp | C/T | 0.0689305 | 0.172377 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147867842 | GCACTCCAGCCTGGG[C/T]GACAGAGTGAGACTC | 79658 |
| rs75669754 | snp | A/C | 0.0644693 | 0.167566 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147950896 | GAAACTTCTTTTAAG[A/C]CTGGAAATTGTAATG | 79658 |
| rs75669915 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147917674 | TTATTCTAGATTAGG[G/T]TGTATATTTTATAGA | 79658 |
| rs75682900 | snp | A/T | 0.046775 | 0.145601 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147991221 | CCGCTTCTCTGGGTA[A/T]GTTAGCGGTCCTTAG | 79658 |
| rs75702255 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147739581 | ATTCACAATAAAAGA[A/C]GACGACCAGAGACAT | 79658 |
| rs75742953 | snp | C/G | 0.0741063 | 0.177655 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147991911 | CATAAAGATTCATAG[C/G]CTTTCCTCTTTTGCT | 79658 |
| rs75746892 | snp | G/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147870576 | ACTTTTTTTTTTTTT[G/T]TGAGAAATTGAGTCT | 79658 |
| rs75759772 | snp | A/G | 0.081446 | 0.184634 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147990880 | AACGGGCCTGGTGTT[A/G]TGGTGCATACCTGTG | 79658 |
| rs75764360 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147805496 | AGAATAGTTTTTCTA[A/G]TTCTATGAAGAATGT | 79658 |
| rs75773364 | snp | C/G | 0.0505692 | 0.150756 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147808822 | CCTTTTCTCCCTCTG[C/G]CCCCTCCCTTCTGTT | 79658 |
| rs75782353 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148069569 | TCTTTTATTAATACC[G/T]AGTCTGTGCTTGCGC | 79658 |
| rs75796272 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147790547 | ACTAGATTAATAATT[C/T]GACTTTTTTCTACCT | 79658 |
| rs75800826 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148048468 | TGCTGAGGATTGTGG[A/G]TTTAAATCCTACATT | 79658 |
| rs75800990 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148017426 | AAACTATGTTTACCA[C/G]GTATAGACAGTACCT | 79658 |
| rs75835276 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147749000 | ACATAAGATAACTTT[A/T]ACTTTTGAAACTCAC | 79658 |
| rs75836572 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147745288 | TTGGGTACGGATAGC[C/T]CTCCTAAATTATTTG | 79658 |
| rs75841859 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147748123 | GTAATCTAAACCCAG[A/G]TACTCTTGAGAAGTA | 79658 |
| rs75851130 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147812315 | CCCTCTTTGAACACA[A/G]CTAGTTTTCAGGAGG | 79658 |
| rs75862873 | snp | A/G | 0.0850919 | 0.187897 | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147782280 | GGCGTGTTGAACTAC[A/G]TTGAGTTTTCATGAG | 79658 |
| rs75875518 | snp | C/G | 0.0573587 | 0.15934 | downstream-variant-500B | ARHGAP10 | GRCh38.p7 | 4:148072884 | TCTCTCTGCTGTTGG[C/G]CTGCTCACAGGTAGA | 79658 |
| rs75902022 | snp | C/T | 0.021333 | 0.101051 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147804782 | GAACTTTTCAAAAGA[C/T]GACATACATGTGGCC | 79658 |
| rs75938467 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148051355 | TCATTTTTTCCCCAC[A/G]ATAAGGTAGTTTTCG | 79658 |
| rs75955913 | snp | C/G | 0.0667028 | 0.170006 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147851974 | AGTGACTTAAGGCCT[C/G]TAAGTCTCAGTTTCC | 79658 |
| rs75960535 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147896875 | GAAGTATTTTTTAAA[A/G]ATTCCAAATGGCTGG | 79658 |
| rs75963497 | snp | C/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147977811 | TCTCTCTCTCTCCCC[C/T]TCCCCCTCCCCTTTT | 79658 |
| rs75984929 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147890154 | TAGTTGCAAGGGAGG[C/T]TTCTAAATCCTAAGG | 79658 |
| rs75988127 | snp | C/T | 0.152001 | 0.229992 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147844982 | CAGAGCCCACAAGGC[C/T]CGGCACGCTCTGATC | 79658 |
| rs76001514 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147914592 | TTTAACATCTTCAGC[A/T]TTTTTGTACAAATGG | 79658 |
| rs76010485 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147969311 | TTTATGGATGTGAGA[A/G]GTTTTGTTTTGCCTT | 79658 |
| rs76014141 | snp | C/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147969327 | GTTTTGTTTTGCCTT[C/T]TTTTTTTTTTTTTTT | 79658 |
| rs76015456 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147995489 | TTGCCACATGTTACC[A/G]TATATTATGTTTTCC | 79658 |
| rs76017069 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148021143 | TCTGGAGACCAACCC[A/G]GGTTGGACCCAGCCC | 79658 |
| rs76033915 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147885178 | AAGACAGTAAAATTA[C/G]TTTGGGTCATTGTAT | 79658 |
| rs76043087 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147873431 | CATATGTGTATATAT[A/G]TTATACACACATGGG | 79658 |
| rs76066654 | snp | C/T | 0.0663309 | 0.169604 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147851708 | CATACAGCATAGTAT[C/T]AGAGGCCCTGAGATA | 79658 |
| rs76072543 | snp | A/T | 0.0193772 | 0.0965046 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147790047 | AGCTCAGGCTGCCAT[A/T]ACAAAATACCACAGA | 79658 |
| rs76076505 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147915946 | CTGTCTGTATAAAAA[A/T]TTTTTTAAAAAAATT | 79658 |
| rs76086241 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147891478 | GGAGTGATGGCTAAT[A/G]GGTACAGGTTTTCTT | 79658 |
| rs76091072 | snp | A/G | 0.0733688 | 0.176922 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147956840 | TTTTAAATGACCACA[A/G]TCATTAGTATTATTA | 79658 |
| rs76104623 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147855414 | GCAGAAAAGAGAGTA[A/G]CTATGTAATATCAAT | 79658 |
| rs76106161 | snp | A/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147818582 | AAAAAAAAAAAAAAA[A/T]AAAGTTAGTTTGTTA | 79658 |
| rs76143204 | snp | A/T | 0.300926 | 0.244758 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147748594 | TTTGGATGTGATAGC[A/T]TTGATAATGATGGTG | 79658 |
| rs76156969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147971731 | GGAGGTTGAGAATGC[C/T]GCTTTAGGACTTTTG | 79658 |
| rs76168260 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148026090 | ATTTGAGGAACTGGA[C/T]TGGATGACTGGAGAT | 79658 |
| rs76170971 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147872569 | GTAACTTTTGACTTC[C/T]CCCAAATTTGACTAC | 79658 |
| rs76175519 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147821777 | AGACACACAGGAAGA[C/T]AGCAGCTGTGTGAAG | 79658 |
| rs76181806 | snp | G/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147761033 | TTTTTTTTTTTTTTT[G/T]TGACACAGAGTCTTG | 79658 |
| rs76189473 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147971377 | AGACAGTCCAGTAGG[A/G]GAAAGAAGAAATGTC | 79658 |
| rs76200988 | snp | C/T | 0.3748 | 0.216622 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911994 | ATTTAAGAACATTCA[C/T]GTGTGTGTGTGTGTG | 79658 |
| rs76205193 | snp | C/T | 0.0592355 | 0.161582 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148069601 | AGTGTGTGGTGTGTA[C/T]AGGGTAGGAGGAGAA | 79658 |
| rs76222724 | in-del | -/TTT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148050536 | CACCACCACGCCTGG[-/TTT]CTAATTTTTTGTGTT | 79658 |
| rs76227551 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147805952 | AGATTATTTACTCTC[C/T]AACCCTGAAGGCTAA | 79658 |
| rs76227849 | snp | A/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147895163 | TAGAAGTCATGGGCA[A/T]TTTTTTTTTGGTGTT | 79658 |
| rs76239182 | snp | A/G | 0.163564 | 0.234582 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147972989 | CGAACTCCTGATCTC[A/G]AGTGATCCACCGGCC | 79658 |
| rs76246628 | snp | A/T | 0.0482946 | 0.147699 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148060935 | CTGCTGATTCTGTGT[A/T]CCTGTTTTGGGATGA | 79658 |
| rs76262383 | snp | A/G | 0.0792508 | 0.182605 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147882179 | TAAAAAATAACCTTG[A/G]AGGCCAGGTGCAGTG | 79658 |
| rs76273537 | snp | A/C | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147818568 | TGAAACTGTCACCAA[A/C]AAAAAAAAAAAAAAA | 79658 |
| rs76277205 | snp | G/T | 0.0803491 | 0.183626 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147998208 | GAAGGATAAAAGAGA[G/T]AAACTGTGGGCTAGT | 79658 |
| rs76296072 | snp | A/C | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147767727 | AATGAGATTACATAC[A/C]TGAAAAAATAAAACA | 79658 |
| rs76296361 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147841950 | CTCCCACGTCACCCC[C/T]AAGATGGAGTCTTGC | 79658 |
| rs76325021 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147845258 | AATGCATTCCTCACT[A/G]TACTCCTACTTTTCT | 79658 |
| rs76331492 | snp | C/T | 0.0509478 | 0.151255 | intron-variant, synonymous-codon | ARHGAP10 | GRCh38.p7 | 4:147854818 | CATACCATATATGGA[C/T]GAAGATATTTCTATT | 79658 |
| rs76360005 | snp | C/T | 0.0722614 | 0.17581 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147999857 | GATTAAAAGGAATTA[C/T]CAGAATGGATAGCTT | 79658 |
| rs76361146 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147855257 | TGGCTAGGACTGCAG[C/T]TTGGGTCTTCTGACA | 79658 |
| rs76363573 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889426 | TGCCTCAGCCTCCCA[A/G]GTAGCTGGGATTACA | 79658 |
| rs76365133 | snp | C/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147976556 | GTTTTTTTTTTTTTT[C/T]CTTCTTCTCAGCAGG | 79658 |
| rs76366413 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147803641 | CTCTACCTCCATGAG[A/G]TCAACTTTATTGGCC | 79658 |
| rs76370445 | snp | G/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148010116 | CTCCACTTTTTTTTT[G/T]TCATGAGGTTGGAGG | 79658 |
| rs76371736 | snp | A/C | 0.040671 | 0.13668 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147834966 | ACTAACAAAAATGAA[A/C]CATTTGGAGTAAAAG | 79658 |
| rs76376257 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147925431 | AGTTTGAGTCTCTTT[C/T]TGATTTATTGTAGTA | 79658 |
| rs76385065 | in-del | -/TATAAAATATATATTATAAATAT | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147784860 | ATATTATAAATATAT[-/TATAAAATATATATTATAAATAT]ATTATAAAATATATA | 79658 |
| rs76404373 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147806125 | GACGGAGCTGAGTGA[C/G]TGAATCCAGGCAGGG | 79658 |
| rs76405273 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147778222 | TGAATTTCCTCACCT[C/T]TGAAAGAGTGGGTGC | 79658 |
| rs76406342 | snp | C/T | 0.0898077 | 0.191933 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147817556 | TCTCCATGTGGTATC[C/T]TACCTCTCAAACTCA | 79658 |
| rs76413235 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147764315 | TTAGACTTGGAGATA[A/G]GTGAGGCTGGAGACC | 79658 |
| rs76416891 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147982573 | TTTTTTTTTTTTTTG[G/T]TATTTTGTGTTGAGA | 79658 |
| rs76424856 | snp | A/G | 0.150333 | 0.229274 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147848451 | AGCTTTCACTTCTGC[A/G]ACCTTGACTAAGTAA | 79658 |
| rs76433445 | snp | A/G | 0.0733688 | 0.176922 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147872648 | ATTACCACACATTTT[A/G]TGTGTTCTATGTATG | 79658 |
| rs76451865 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147952781 | GTTCATCAGTTTTTC[C/T]TTTTATGGACTGTGC | 79658 |
| rs76464399 | snp | C/G | 0.0364509 | 0.129988 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148019402 | AATCCCTGTAGTACA[C/G]GCATTATGGTTCTCA | 79658 |
| rs76521020 | snp | G/T | 0.0228947 | 0.104514 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147743269 | CGAATGCTTGACCTC[G/T]TGATCCACCCGCCTC | 79658 |
| rs76525018 | in-del | -/TTT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148034499 | ATTTTTTTTTTTTTT[-/TTT]GTATTTTTAGTAGAG | 79658 |
| rs76528715 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147919397 | GTTTTGGCATGTGTG[A/G]GAGTCACATCAACTC | 79658 |
| rs76530427 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147945339 | TAGAACTTACTAGCC[A/G]TTTTGAATTTTCTTC | 79658 |
| rs76532761 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147966397 | TGGTGTCTGTAGGGA[G/T]TCTGGCATCAATTCC | 79658 |
| rs76547287 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147888257 | GCCATCCGTATGTTG[A/G]TAACTTGCAAATTTA | 79658 |
| rs76552483 | snp | A/C | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147998931 | CCCTGGAAGAACTAG[A/C]CAAGAAGAGAGAAGA | 79658 |
| rs76558092 | snp | A/G | 0.0663309 | 0.169604 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147851074 | TGGATGCAACTAACT[A/G]GATTGAGAATGGAAT | 79658 |
| rs76564917 | snp | A/G | 0.0618563 | 0.164627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147955708 | AATGGCATGAGCAAA[A/G]TGCTGAGGGAACACA | 79658 |
| rs76569727 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147852665 | TTGACGTAAACAAAA[C/G]TTTTTATGTCATATT | 79658 |
| rs76574292 | snp | G/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147768755 | TCTTTTTTTTTTTTT[G/T]TGGCAGGGAATCTTG | 79658 |
| rs76611239 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147777917 | ATAAAACTTGAGGAA[C/T]TGGAATCCTCATGCT | 79658 |
| rs76645385 | snp | G/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147919588 | TTTTCTTTTTTTTTT[G/T]TGGAGATGCAGTCCC | 79658 |
| rs76654940 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147896164 | ATGAGAGATGTGTGC[A/G]TTATGATCTTCATTT | 79658 |
| rs76656138 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147984869 | GCACAGTGGTCTGAG[C/T]GCCCTGCTCCAACCT | 79658 |
| rs76658248 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147799313 | CCTAATGCTGGGATG[A/G]CCTCTCTTTGTTTAT | 79658 |
| rs76665662 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148054866 | GTGGATTTTTCTGAG[C/T]GGAGTATCTGTGTCC | 79658 |
| rs76666635 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148027537 | AATACTACTGTTGAG[C/T]GGGGCAGAGATGGAT | 79658 |
| rs76667703 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147951420 | TTTTTTTTTTTTTTC[A/T]TTTTCTTTGTGAAAT | 79658 |
| rs76677444 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147953698 | TGATTATCTTAAAAG[A/T]TATGGTTTTGGATTA | 79658 |
| rs76683244 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147844554 | TCTCACACATGGGAG[A/C]TAAAAGTTAAAACAA | 79658 |
| rs76696106 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148058398 | TTCTTTTCTTAATGC[A/G]TATTCTCCTCGCTCT | 79658 |
| rs76714223 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911696 | ACAAGAATTGTCATT[A/C]ATTAAGGATATACAG | 79658 |
| rs76726928 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147853863 | GTTTACTTGTGACTC[C/T]TTCAATCCATCTGGA | 79658 |
| rs76749408 | snp | A/C/G | 0.00358923 | 0.042236 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147890190 | AAATTGCTGTCTTTT[A/C/G]TTTTCAGAGGTCCAT | 79658 |
| rs76769475 | snp | A/C | 0.0349115 | 0.127424 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147839270 | ACATTAGAATTGGAA[A/C]ACAGAATTTTCCCTT | 79658 |
| rs76778483 | snp | C/T | 0.0752113 | 0.178743 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148069030 | ACACTGAGACTGCCA[C/T]GTTCTCCACCCATAA | 79658 |
| rs76797526 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147941175 | AAGAGTATATTGATA[A/G]CAGAATGGGAAATGT | 79658 |
| rs76802479 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148043101 | ACCAGGTTATAAAAC[C/T]AGTATATGATGGCGA | 79658 |
| rs76836671 | snp | G/T | 0.0360663 | 0.129354 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147868093 | GCTGTGGTCTCACAA[G/T]TTGTGAAAACAGTTA | 79658 |
| rs76846050 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147896742 | CTTGTTTTTGAGATG[C/G]GCATTTGAATCTATA | 79658 |
| rs76847375 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889429 | CTCAGCCTCCCAGGT[A/G]GCTGGGATTACAGGC | 79658 |
| rs76860652 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147780113 | ATTTTCAAAGTAATA[C/T]GTGCTCATTGTAGAA | 79658 |
| rs76888325 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147849238 | TTAAAAGACTCTGCT[C/T]TTTTTTTTTTTTTTA | 79658 |
| rs76895095 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147896849 | GCTATAGATCGAAAA[C/T]GTGATATTTAGAAGT | 79658 |
| rs76906713 | snp | C/G | 0.0168055 | 0.0901129 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147912705 | CTGTCACCCAGTGCA[C/G]TGGTATGATCATAAC | 79658 |
| rs76907971 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147774161 | TGGCACATAGTTAGC[A/C]CTGTATAAAAATGTT | 79658 |
| rs76908336 | snp | C/G | 0.0479149 | 0.147179 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147842852 | CCTTTTCCCTTCCTT[C/G]CTGGAGAAAATCCCA | 79658 |
| rs76915474 | snp | G/T | 0.375 | 0.216506 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147920191 | GGAGGTCGAGGTGGG[G/T]GGATCACCTGAGGTC | 79658 |
| rs76933341 | snp | A/C | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147983958 | TTTGTTATTGTTTGG[A/C]TGAGAGTTCTTGATT | 79658 |
| rs76938699 | snp | A/G | 0.093777 | 0.195178 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147985302 | TGGGTGGCTCAGGCT[A/G]CTGATCCAGGTGAGC | 79658 |
| rs76947806 | snp | C/T | 0.228842 | 0.249103 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147973757 | AAATTGTTTCAGTTT[C/T]TTGCTCCCACAAATA | 79658 |
| rs76953078 | snp | A/G | 0.159951 | 0.233219 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147815858 | GTGACAGAGTGAGAC[A/G]GTCCTGCTGACACCT | 79658 |
| rs76953492 | snp | G/T | 0.0146672 | 0.084371 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147793510 | GCCTTGAAAGGAGGA[G/T]TTGGACCTGGGATCT | 79658 |
| rs76955305 | snp | A/C | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889416 | GTGATTCTTCTGCCT[A/C]AGCCTCCCAGGTAGC | 79658 |
| rs76960646 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147954595 | AATATCTTGCGAGAT[A/T]ACCCTCCAGAAAGGC | 79658 |
| rs76993576 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147984931 | CAGGCAGGCCCACCT[A/G]CAGGTCCCCCAATGG | 79658 |
| rs77041827 | snp | A/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147767728 | ATGAGATTACATACC[A/T]GAAAAAATAAAACAT | 79658 |
| rs77044362 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147844653 | GCCAGAAATCTGGGA[A/G]GGATCCTGGAAATCT | 79658 |
| rs77049699 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147948090 | AGATTACAGGCACTC[A/G]CCACCATGTCCGGCT | 79658 |
| rs77059630 | snp | A/G | 0.0614824 | 0.164198 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147952430 | CTCTTAAGCTGGTCA[A/G]TCTTTTTCATTTTAG | 79658 |
| rs77059657 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147786361 | CCACCTGAGTAACTG[C/T]CCGGTGAGACTGGGA | 79658 |
| rs77060274 | snp | G/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147768758 | TTTTTTTTTTTTTTG[G/T]CAGGGAATCTTGCTC | 79658 |
| rs77063685 | snp | A/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147909643 | GCTTATAAAAATGTA[A/T]TTTTTTTTGTATGGT | 79658 |
| rs77076922 | in-del | -/A | 0.153332 | 0.230554 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147843457 | CACCTTGCCATGGAT[-/A]TTGCTGAGCTCTCAT | 79658 |
| rs77084502 | snp | G/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148012923 | GGTGGGTATCTGTCT[G/T]GTTTTTTTTTTTTTT | 79658 |
| rs77097440 | snp | A/C | 0.0988009 | 0.199095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147838484 | CTCTTAAAAAAAAAA[A/C]ACACACACACACACA | 79658 |
| rs77113106 | snp | A/G | 0.0655868 | 0.168795 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147901376 | ATGTTAAAGTAATGC[A/G]TTGCAAGTGTGAAGT | 79658 |
| rs77136496 | snp | C/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147799047 | TGTCCTTTTTTTTTT[C/T]TCTTCGAGATGGAGT | 79658 |
| rs77136575 | snp | A/G | 0.0633504 | 0.166319 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147836608 | TAATTTATAGCACCT[A/G]AGCACCTGTGTCCCA | 79658 |
| rs77158691 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147780560 | GAAGAAGGAGACTAG[A/G]AAAAAAAGACTGAAC | 79658 |
| rs77160448 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148068505 | TCTGAGAAAAAAATA[C/T]CGAGTGAAAAAATAA | 79658 |
| rs77162961 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889446 | CTGGGATTACAGGCA[C/T]ACACCGCCACGCCCG | 79658 |
| rs77195333 | snp | A/T | 0.0858192 | 0.188533 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147999941 | GTTTTTTTTTTTTTT[A/T]AAATTATACTTTAGT | 79658 |
| rs77196060 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147914292 | GAAAATTTCTGTTTC[C/T]CTCACTGAGTTCTTT | 79658 |
| rs77210196 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147862680 | GGGTGGTGATAGAGG[A/T]TGACTGGTAATGCAA | 79658 |
| rs77214072 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147849237 | TTTAAAAGACTCTGC[C/T]TTTTTTTTTTTTTTT | 79658 |
| rs77219098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148039105 | ATTTTGGTTATGTTA[C/T]TTTCCTTTTCTTTTG | 79658 |
| rs77236889 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148025384 | TTTTTTTTTTAAGTT[G/T]TCAGAATCAGGAAAA | 79658 |
| rs77250666 | snp | A/G | 0.0663309 | 0.169604 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147849977 | GGTGGGGACTTGGAG[A/G]ACTTTTCTGTCTAGC | 79658 |
| rs77259326 | snp | A/T | 0.0283406 | 0.115616 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147794515 | GTAGCATCCAGAGCA[A/T]AACAGAACATATACA | 79658 |
| rs77266227 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147876855 | GCCCTATGAAGTATA[A/G]GGTACTATTACTGTT | 79658 |
| rs77276930 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147906908 | ACATATAAGACTAGT[A/G]TATCATTAGTTTTTA | 79658 |
| rs77278375 | snp | A/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148042150 | TGCTCCTTGTTTTTT[A/T]ATTCCCTATTTCAGT | 79658 |
| rs77296211 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889865 | ATTTGGTTGCATGTA[A/G]CAGAAAAAGTCAAAA | 79658 |
| rs77299897 | snp | A/G | 0.0700422 | 0.173537 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147930296 | TTCTCCTTTGTTGTT[A/G]TATCTTTTTCTGTCA | 79658 |
| rs77312033 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148043094 | ACCTAAAACCAGGTT[A/G]TAAAACCAGTATATG | 79658 |
| rs77314624 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147983579 | AATTCTTTCTTTTGC[A/G]TGGTCTCATCTGCCG | 79658 |
| rs77316842 | snp | C/T | 0.102014 | 0.201495 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147862822 | CAAATGAGGAAATCA[C/T]CCTTCTTATGTCTTT | 79658 |
| rs77349773 | snp | G/T | 0.0240643 | 0.107019 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147870801 | GGAAGGAAATACAGT[G/T]TGCAAAATTTTAGGA | 79658 |
| rs77352317 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147750395 | GAAGAAAGAATGGAA[C/T]GGGATTAATACATAA | 79658 |
| rs77384670 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147796440 | AGAGACAACAACGGA[A/G]CTTCCTCTTAGAGGA | 79658 |
| rs77404396 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147814995 | AACCAGGCTTTCTTG[A/G]CGTCGAAGCCAAGAA | 79658 |
| rs77407170 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147901492 | ACAAATGGAATTCTT[G/T]CCTTGTGAATGATCC | 79658 |
| rs77409685 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147843066 | TAGCCATTTGGTAGC[A/G]ACTCTCAGCTTTTTG | 79658 |
| rs77412028 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147946410 | TTTTTTGCTTTGATC[C/T]CTACTACAGATTTTA | 79658 |
| rs77448759 | in-del | -/CCC | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147914566 | TGCGCTCCCCCCCCC[-/CCC]TTTTTTTTTTTAACA | 79658 |
| rs77459396 | snp | C/T | 0.0919752 | 0.193722 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148064777 | TCATCTCTCTCCTGA[C/T]GGGAAGAAGCTAGTG | 79658 |
| rs77485679 | snp | C/T | 0.152001 | 0.229992 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147846262 | CATTAAGAATCTTTT[C/T]CTATTCCAAATCACT | 79658 |
| rs77487968 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147921662 | TCATTGTGTCAGAAG[A/C]CAAAAGCAGTTACAA | 79658 |
| rs77508207 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147807047 | CAGTGCCATTTAGTG[C/T]GGGGGCAGGTAATTC | 79658 |
| rs77515906 | snp | C/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147808338 | GCATTTTTTTTTTTT[C/T]CCAGGAACAGAAGGG | 79658 |
| rs77521627 | snp | A/G/T | 0.0433465 | 0.140692 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147886518 | TGTTGTTCGTCGTGC[A/G/T]CTCACTTTCTTCCTT | 79658 |
| rs77523887 | snp | C/G | 0.444444 | 0.157135 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147914543 | CTATTTTTTAATTAC[C/G]CATGTTCTGCGCTCC | 79658 |
| rs77527396 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147767512 | TTAAAAAATAGCTGG[C/T]TTTGCTCCTATAAAG | 79658 |
| rs77581990 | snp | C/T | 0.444444 | 0.157135 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148055104 | GAAGGAAGGTAGGAT[C/T]CAAGGAGAACTCTTT | 79658 |
| rs77598068 | in-del | -/GT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147999926 | GCTCCTATTAACAGT[-/GT]TTTTTTTTTTTTTTA | 79658 |
| rs77601198 | snp | A/G | 0.0693013 | 0.172766 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147847510 | GAATAGAAGGAGCTT[A/G]TTACTGGGGGGAGTG | 79658 |
| rs77606865 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147795003 | CTATAGTCAGTTCCA[C/T]ATAGTGTGGCAGCTA | 79658 |
| rs77611272 | snp | G/T | 0.0267878 | 0.112589 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148028132 | AAGTCTGTAGGGGGT[G/T]CTTTCTGGTTTCCTT | 79658 |
| rs77618404 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147775214 | CACCGCACCGGCCTG[A/G]TGGTCATTAAGTGCC | 79658 |
| rs77637354 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147783667 | AGAACACATTAAATT[A/G]TGTATTGTATAATTT | 79658 |
| rs77653564 | snp | A/C | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147783781 | ATTATATTTATATAA[A/C]ACACATTAAATTATG | 79658 |
| rs77667290 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148016079 | AAGTCAAGCACTTGG[C/T]ATAATGTCAGGCATG | 79658 |
| rs77711987 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911842 | ATAAAATATTATTTT[A/G]AAAGCTTGGAGCATG | 79658 |
| rs77723329 | snp | C/T | 1.64757e-05 | 0.00287012 | missense, utr-variant-5-prime, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147822756 | CAGCGGAAGTTTGCT[C/T]ATTCACTCAGAGACT | 79658 |
| rs77727364 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147901766 | TCAACAGTTATTTCT[A/G]TGTTTTAGGTTACTA | 79658 |
| rs77739246 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147855047 | GATTAAATCAAATAA[C/G]GTGGTAAAAATGTTT | 79658 |
| rs77742673 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148011914 | ATTACATAAAAATCT[A/G]TGTGCTAATCCCCCA | 79658 |
| rs77743884 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147893844 | GAGTGGGTAGAATTA[A/G]AAACAGCATTTCTAG | 79658 |
| rs77762492 | snp | C/T | 0.0655868 | 0.168795 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147944500 | TTCAGAAAGTTTCAG[C/T]CCAACATTGAGTTGT | 79658 |
| rs77768411 | snp | G/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147919763 | TTTTTGTATTTTTAG[G/T]AGAGGTGGTGTTTCA | 79658 |
| rs77781709 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147896401 | ATGATATTCAGATTT[C/T]CTATTTTTCTTGGGT | 79658 |
| rs77795867 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147764499 | GTAAAAAAAAAAAAC[C/T]TCCAAATCTGGAATC | 79658 |
| rs77797032 | snp | G/T | 0.067446 | 0.170804 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147958301 | TGACAACTAAAGGCT[G/T]AATGCCTGTTGTATC | 79658 |
| rs77856376 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147882696 | TTCAAAGGTGAATTC[C/T]TTTTTTTCCTTATTG | 79658 |
| rs77858603 | snp | A/G | 0.0528381 | 0.153711 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147821772 | GAAGGAGACACACAG[A/G]AAGACAGCAGCTGTG | 79658 |
| rs77883533 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911002 | CTTTTCTTCCTTCCT[C/T]CCTCCTCCTCTTCCT | 79658 |
| rs77889855 | snp | C/T | 0.270351 | 0.24917 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147999007 | CACTATCCACAGATA[C/T]GATTGTGTACATAGA | 79658 |
| rs77908951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147896476 | TTGACTTTATTGGCA[C/T]AAATGTCATATCTAC | 79658 |
| rs77913055 | snp | A/C | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147910349 | TTGTGAGTCTTTCTC[A/C]AAAAAAAAAAAATTG | 79658 |
| rs77913334 | snp | G/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889481 | ATTTTTGTATTTTTG[G/T]TAGAGATGGGGTTTC | 79658 |
| rs77923277 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148036425 | GGAGGGACCCAGTGG[A/G]AAGTGATGAATCACG | 79658 |
| rs77934553 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147787455 | GAGTGATGGAAGCGG[G/T]GGGGGAGGAGGCTCG | 79658 |
| rs77936882 | snp | G/T | 0.0633504 | 0.166319 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148024136 | CCCATTGCTAATTTG[G/T]AATCATATGGTTATT | 79658 |
| rs77938127 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148009349 | GTTGACCAGGCTGGT[C/T]TCGAACTCCTGACCT | 79658 |
| rs77939149 | snp | A/T | 0.0114959 | 0.0749385 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147909699 | TTTGCTGATTTGATT[A/T]AAAAATTCTGTTTTT | 79658 |
| rs77954836 | in-del | -/TT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911948 | CTAGGTTTTTTTTTT[-/TT]AAAGGATTGTGTTCT | 79658 |
| rs77995339 | snp | A/T | 0.152001 | 0.229992 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147845480 | TTAAAGTTTATTAAG[A/T]TGGCAACTTTGGAGA | 79658 |
| rs77996806 | snp | A/C | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147867867 | AGACTCTGTCTCAAA[A/C]AAAAAAAAAAAAAAA | 79658 |
| rs77997727 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889488 | TATTTTTGTTAGAGA[C/T]GGGGTTTCACCATAT | 79658 |
| rs78064921 | snp | A/G/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147919568 | ATCTTTTAAAAACAA[A/G/T]TTTTTTTTCTTTTTT | 79658 |
| rs78071235 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147938943 | ATGAATTCCCATATT[A/C]TCATCCAGATTCAAT | 79658 |
| rs78072816 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147930488 | AGATAAGAAAGAACT[C/T]CTTGGCCTATTTAGT | 79658 |
| rs78087548 | snp | A/T | 0.291235 | 0.246576 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147974557 | TACAATTCAGATTAC[A/T]TTGATCTTATTGAGG | 79658 |
| rs78112698 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147744886 | ACACCATATGGATGG[C/G]AAACGATGCCATGCA | 79658 |
| rs78132591 | in-del | -/AG | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147898188 | GGCTGCCTTAGGCTG[-/AG]CATTTCTTGTAATGC | 79658 |
| rs78137022 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147932890 | CTCCAGGCAGGTTTG[G/T]TGTGGAAATTACTTT | 79658 |
| rs78160800 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147924800 | ATAAGGATCAGATCT[C/G]CTTCATGGGGTTGTT | 79658 |
| rs78164058 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148029287 | AGGCTCATATTAAGG[A/G]ATGGGAGGCCACTCA | 79658 |
| rs78174941 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147806973 | AAGTCTCTAGTAAGC[A/G]TGAAACCCGGTGAAA | 79658 |
| rs78181235 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147969717 | CACCTTGTTAATAAA[C/T]CTTACAGGAATTTTC | 79658 |
| rs78189210 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147787358 | GAGTATTTTCAGTTT[A/G]GGAAACACATGAACA | 79658 |
| rs78190867 | snp | A/G | 0.0633504 | 0.166319 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147887550 | ATTCTTCAAAAAGCT[A/G]TCATATTTATGGTCT | 79658 |
| rs78191921 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147919031 | CCTCCAATTGCTTCC[A/G]AAGGTGGCTCAGTTC | 79658 |
| rs78214040 | snp | G/T | 0.0524604 | 0.153226 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147896155 | TTTATGTTCATGAGA[G/T]ATGTGTGCGTTATGA | 79658 |
| rs78223604 | snp | A/T | 0.0581099 | 0.160244 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147821303 | TGGGAAATAGATGAG[A/T]TTCCATGGGAGGAGC | 79658 |
| rs78223837 | snp | C/T | 0.0566069 | 0.158427 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147836383 | AGGATTGAAAGTTGA[C/T]AAAATTCTTACTGGG | 79658 |
| rs78227712 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147815588 | CAGGCTGGGCACTGT[C/G]TCTCACACCTGTAAT | 79658 |
| rs78246940 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889480 | AATTTTTGTATTTTT[A/G]TTAGAGATGGGGTTT | 79658 |
| rs78250017 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147776948 | GAGAGAGCGTGTCTT[G/T]CCTTCCTGGTGGCCT | 79658 |
| rs78251381 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147865126 | GTCAAGGAATTGCCT[C/T]TAAATCAGTGGTTCT | 79658 |
| rs78266135 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148065842 | GACACAACTGTTTGA[A/G]TCAATCATGAAGATG | 79658 |
| rs78282648 | snp | C/G | 0.0667028 | 0.170006 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147857020 | ACCACACCCTGCTAA[C/G]TTTTGTATTTTTAGT | 79658 |
| rs78283456 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147909924 | ATAATCCTCTRTTGC[A/G]TGTGTTCTGTTTTAC | 79658 |
| rs78288637 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148054523 | ACCCCAACTTCCTGG[C/T]TCATCAGTTACATAA | 79658 |
| rs78294755 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147848147 | CCTTGGTGGAAATAA[A/G]CACTGTGGCCTCAGT | 79658 |
| rs78299570 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147744953 | GAGAAGGCAGGGAGA[A/G]GGTCAGGGCAAATCC | 79658 |
| rs78309357 | snp | G/T | 0.0146672 | 0.084371 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147991752 | AACAGGTCCAAGTTT[G/T]CAGGCAGGCCTTTCT | 79658 |
| rs78320242 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147782136 | CCACATTGCCATAAG[A/G]TGAATGTCCTGCAGA | 79658 |
| rs78334046 | snp | A/T | 0.0189856 | 0.0955633 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148031074 | CAACAACAACAACAA[A/T]AAAATGAATTTTGAG | 79658 |
| rs78335024 | snp | C/G | 0.220544 | 0.248259 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147770971 | GTCTTACCTCTGTGC[C/G]TGTATCTTTGTCCTA | 79658 |
| rs78337743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147976995 | AATATTTATAATAAT[A/G]AGAACATGTTCATGT | 79658 |
| rs78348867 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148015300 | GGCAAGATAGGAAGT[A/G]GCAGTTGGCTGTGAG | 79658 |
| rs78360374 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889895 | ACAAAATGGCTTAAA[C/T]GGGGTTAAAGTTTAT | 79658 |
| rs78377788 | snp | A/G | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147968381 | AACACTTATTCTTTA[A/G]GGCAGTACTTTTCAA | 79658 |
| rs78387706 | snp | A/G | 0.0633504 | 0.166319 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147986600 | GTACACCCCACAGCC[A/G]AGACAGTCTCTCTAG | 79658 |
| rs78401137 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147990347 | CGAATGAATGTTAGC[C/T]AGAAAATGGCTAAAC | 79658 |
| rs78414658 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147775604 | CCTTTTCACCCAGAA[A/G]GCAGAGTGGGTATAT | 79658 |
| rs78434180 | snp | A/G | 0.0792508 | 0.182605 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148003954 | GCAAAATTATGCTAA[A/G]AGACGTGAGAGAAAT | 79658 |
| rs78442989 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148014998 | AGTCAGGGCCTGAGC[C/G]TGTGGGATGGGTGAC | 79658 |
| rs78453474 | snp | A/C | 0.0854556 | 0.188216 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148006200 | TGCCAAGCATTGAGG[A/C]AGCCCATGCTCACCG | 79658 |
| rs78470840 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148045409 | GAGCTAGCTTAATCA[G/T]AGCCTGGAATTTCTC | 79658 |
| rs78531415 | snp | C/T | 0.108048 | 0.20579 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147793776 | ATCCGTGCCTGTGTA[C/T]GTGCCTTCCCCCTTA | 79658 |
| rs78534864 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147744045 | GTTTGTGAGAAGAAA[C/T]GTGTATATTAGTGCA | 79658 |
| rs78562948 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148031903 | TGATATTAAGTACTG[C/T]AAAAGCATTTTATTG | 79658 |
| rs78567986 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147976555 | GGTTTTTTTTTTTTT[C/T]TCTTCTTCTCAGCAG | 79658 |
| rs78569028 | snp | G/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148020548 | ACATGCGTTTTTTGT[G/T]TTTTTTTTTATTCCT | 79658 |
| rs78574876 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147855990 | CATTATTTTTGCTTT[C/G]GAAAATACAAGTTGG | 79658 |
| rs78619931 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147738982 | GAGGTTAGGAGCTCA[A/G]GACTAGTCTGGAGAA | 79658 |
| rs78627949 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148035235 | TTTTGGGCAAGCATT[A/T]TGCTTAATTTCTTTA | 79658 |
| rs78644428 | snp | A/G | 0.0633504 | 0.166319 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147837247 | TGTAATTAATTGATA[A/G]TGAATTGGTTTAATT | 79658 |
| rs78658935 | snp | A/G | 0.0667028 | 0.170006 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147860865 | TTGGAGTAGTAAAAC[A/G]TATAGTGATTGCCTT | 79658 |
| rs78661620 | snp | C/G | 0.0777841 | 0.181223 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147974663 | CTCTGATGTTTCATT[C/G]ATTTCCTGATGATCA | 79658 |
| rs78681009 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147943230 | TAGTTTGTGTGGTCT[A/G]GTGAGCTCAGTGGTT | 79658 |
| rs78687125 | snp | C/G | 0.0648419 | 0.167978 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147977097 | ATCTGGAGATGCGGA[C/G]CTGCAAAGAGAGCTC | 79658 |
| rs78702601 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147776510 | CAGGCATGAGCTACC[C/G]TGCCCAGCCTGAGTG | 79658 |
| rs78708796 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889489 | ATTTTTGTTAGAGAT[A/G]GGGTTTCACCATATT | 79658 |
| rs78723951 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148025052 | GAATCGTAATATCCA[A/G]TCAAATTTATTTAGT | 79658 |
| rs78729566 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147845154 | TTGCCCTTTGCACCA[C/T]GGATTCCTTCTCACC | 79658 |
| rs78761969 | snp | A/C | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147818567 | GTGAAACTGTCACCA[A/C]AAAAAAAAAAAAAAA | 79658 |
| rs78790841 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147791437 | TTTAGGAGGAAAAAA[A/G]GCCACATTATTTTTT | 79658 |
| rs78793407 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148034307 | TTGGTAACTAGCATC[A/T]CCCTCTGGCAATTAC | 79658 |
| rs78793767 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148030617 | TTAATAGAACAAAGC[C/T]AACCTGTGGCCAGTT | 79658 |
| rs78804150 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147844843 | TCCGGTTTTCTGTAC[C/T]TTTCATCTCTCCCTC | 79658 |
| rs78838620 | in-del | -/CAACA | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147920124 | ACGTCTTTTAAAAAA[-/CAACA]TAACCTCGCTGGGCA | 79658 |
| rs78839287 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147968779 | TGCTTGGTCACTCAT[C/T]TGTTTATTAAAAAGA | 79658 |
| rs78854719 | snp | C/T | 0.0670745 | 0.170406 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147952912 | TAGTTCTGTGATCCA[C/T]TTTGAGTTAATTTTT | 79658 |
| rs78888960 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147755633 | TGGCGAGCTGCTGGA[A/G]TATTTTAGGAAGTAG | 79658 |
| rs78896655 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147993311 | TGGGAATATAGATGA[A/G]CTAAGATTGGTCATG | 79658 |
| rs78899653 | snp | A/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147959234 | AAAAAGCCCAGAGTA[A/T]TTTTTTTTTTGTTTT | 79658 |
| rs78919355 | in-del | -/A | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147813574 | GTGACATGGCAGCAA[-/A]CCCAGAGTCTGACAG | 79658 |
| rs78920995 | snp | A/C | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148071642 | AAACAAACAAACAAA[A/C]AAAAACACAAAAAGC | 79658 |
| rs78935613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889452 | TTACAGGCATACACC[A/G]CCACGCCCGGCTAAT | 79658 |
| rs78964327 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147899328 | GTGTGTGTGTGCATG[C/T]GTGTGTGTGTGTGTG | 79658 |
| rs78979045 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147772910 | CAGTTTGAGTCATTG[G/T]GTGGGCGGAACTGAT | 79658 |
| rs78991020 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147810578 | GTGGTGCAGAGTTGC[C/T]AGTCTGAGAGATTCA | 79658 |
| rs78997646 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147868392 | CAGGTGCATGCCAGC[A/G]CACCCAGCTAATTTT | 79658 |
| rs79001455 | snp | A/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147924971 | ATTGAAGAACTTTCT[A/T]TTTTTTTTTTTTTAA | 79658 |
| rs79008209 | snp | G/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147947958 | GTTTTTTTTTTTTTT[G/T]TGAGACAGAGTCTTG | 79658 |
| rs79064289 | snp | A/G | 0.0629771 | 0.165899 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147833089 | CCTGGATACAAGAAT[A/G]GAGCTCCTTAAGAGC | 79658 |
| rs79064290 | snp | A/C/T | 0.0263992 | 0.111815 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147860971 | TGAGGGCTGTTGTCA[A/C/T]GGAATTTTTAGGATG | 79658 |
| rs79081369 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148045414 | AGCTTAATCAGAGCC[A/T]GGAATTTCTCTTATG | 79658 |
| rs79124193 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148036537 | CTTTTGCCTGGCACT[C/T]CTCCTTCCTGCTGCC | 79658 |
| rs79128067 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147901237 | ACATGTTCTAGCAAA[C/T]GTTTTATTTTTCCTA | 79658 |
| rs79130509 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147982889 | TTACTTTCTTTTTTT[C/T]CCTGAATTTTCGAGA | 79658 |
| rs79147860 | snp | G/T | 0.0236746 | 0.106192 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148051679 | ACTGAGAGGCTTGGC[G/T]TTGTTTATCCTGAAT | 79658 |
| rs79176115 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147861708 | GACCTGTAGTGCATA[A/G]CTCCTTTCCACAGGC | 79658 |
| rs79184035 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147771724 | TGTCAGTGAAATTGT[A/G]TTTTAAGTATGTAGG | 79658 |
| rs79198254 | snp | A/G | 0.228253 | 0.249052 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147976920 | GAAAGCATACTGAGT[A/G]CAAGTGAGCAGTACT | 79658 |
| rs79210558 | snp | G/T | 0.5 | 0 | upstream-variant-2KB | ARHGAP10 | GRCh38.p7 | 4:147730900 | CTTTTTTTTTTTTTT[G/T]AGACATTGTCTCGCT | 79658 |
| rs79231899 | snp | C/T | 0.0554779 | 0.157039 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147797375 | TGTGCATGTCTGGAG[C/T]TGTTTGTTTTTCTCA | 79658 |
| rs79236135 | snp | G/T | 0.106278 | 0.204558 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147862730 | AACAACCAGGAGAGA[G/T]AATTTACTAAAAGAT | 79658 |
| rs79247023 | snp | C/T | 0.0596104 | 0.162024 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147991447 | CGGAGCTTACTCTTC[C/T]CCAGCAACAAAAATG | 79658 |
| rs79265259 | snp | C/G | 0.0700422 | 0.173537 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147930136 | ATGCCAGGCAATCTG[C/G]TGGTTACTAGATGAG | 79658 |
| rs79267731 | snp | A/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147755989 | TGACCCTGTTGGTAA[A/T]TTTTTTTTTCTGTCA | 79658 |
| rs79280575 | snp | C/G | 0.0807149 | 0.183963 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147995651 | AAAAAATAATAACCT[C/G]GTATCAGTCAGAGAC | 79658 |
| rs79324443 | snp | A/T | 0.106278 | 0.204558 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147862677 | AGGGGGTGGTGATAG[A/T]GGTTGACTGGTAATG | 79658 |
| rs79325966 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147734230 | AGCCAGTTTGGCCAC[G/T]GGTAGAAAGCTATTT | 79658 |
| rs79327073 | snp | A/T | 0.104859 | 0.203554 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147924985 | TATTTTTTTTTTTTT[A/T]AAATAGCAATTTACA | 79658 |
| rs79344048 | snp | A/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147835793 | CTCTTATGTAAAACA[A/T]AAAAAAAATTCAAAA | 79658 |
| rs79369720 | snp | A/C | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148019774 | CACCTAAAAAAAAAA[A/C]AACAAAACAAAAAAC | 79658 |
| rs79370438 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147866368 | TTTTACTTTCTTAAA[A/G]ATTGTGTCAACCTAT | 79658 |
| rs79391866 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147768512 | TAATTAAAAAAAAAA[A/G]GTAATTAAAGGTTGA | 79658 |
| rs79394083 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147849236 | CTTTAAAAGACTCTG[C/T]TTTTTTTTTTTTTTT | 79658 |
| rs79395321 | snp | C/T | 0.0611083 | 0.163768 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147996158 | ACTTCCACAAAGGTA[C/T]AGTCTCCTCCTGATT | 79658 |
| rs79404467 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147970064 | TTTCCCCATTACCTC[A/G]CCTTGTCTCTCCCAT | 79658 |
| rs79410952 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147997025 | GCAGCCCCAGCCGAC[C/T]AATAACCATTCTCTC | 79658 |
| rs79439463 | snp | G/T | 0.0667028 | 0.170006 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147854583 | TTACATTTATATATT[G/T]TTTTCTGTAATGCAG | 79658 |
| rs79440497 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147860217 | GGAGGCCGAGGCGGG[G/T]GGATCACGAGATCAG | 79658 |
| rs79445761 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147854994 | TTTTGACCGCTGATT[A/G]AAGCGTCACCCCTTC | 79658 |
| rs79477018 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147847541 | TAGTTATTTCTGTGC[A/G]CACCTCAGTTTTATG | 79658 |
| rs79482026 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147785994 | ACTTCTTTCTGATTT[C/T]GGGAAAATTGAGATT | 79658 |
| rs79489490 | snp | A/C | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889448 | GGGATTACAGGCATA[A/C]ACCGCCACGCCCGGC | 79658 |
| rs79506668 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147808110 | TGAAGTTAGAAAGTA[G/T]GGATCACACATCCTG | 79658 |
| rs79516735 | snp | A/T | 0.0441095 | 0.141807 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147983805 | TGTCATTTCAGACAT[A/T]CATTCCGGTTAGAAT | 79658 |
| rs79562055 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147795376 | TCCCTTTTTCCTACA[A/C]AACTTCCTGTAAGGA | 79658 |
| rs79588294 | snp | C/T | 0.031825 | 0.122064 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148044896 | CCCTTCTATTGGCGC[C/T]GAGTTTCTCCAATTA | 79658 |
| rs79590127 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147974674 | CATTGATTTCCTGAT[C/G]ATCAGGAGGTTTTTT | 79658 |
| rs79593636 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147984932 | AGGCAGGCCCACCTA[C/T]AGGTCCCCCAATGGC | 79658 |
| rs79593813 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148045410 | AGCTAGCTTAATCAG[A/T]GCCTGGAATTTCTCT | 79658 |
| rs79599413 | in-del | -/TT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148061624 | TAATGTTTTTTTTTT[-/TT]AAATGACCCCCTTTT | 79658 |
| rs79599992 | snp | C/T | 0.0648419 | 0.167978 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147973123 | TGTGAATGAGTGTTT[C/T]GGAATGAGTGATATT | 79658 |
| rs79601068 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147791438 | TTAGGAGGAAAAAAA[A/G]CCACATTATTTTTTC | 79658 |
| rs79629186 | snp | G/T | 0.0267878 | 0.112589 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147884081 | AATTGACAAAGATGA[G/T]CTAGCAGTCTACTAG | 79658 |
| rs79658952 | snp | C/T | 0.046775 | 0.145601 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147864302 | GATGGGCGTCCAGCC[C/T]TGGCCCGCCTTTGAG | 79658 |
| rs79713249 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147734203 | AGAGGTGTGGAGAGA[C/G]GCAGAGGGCAAAGCC | 79658 |
| rs79751415 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147963208 | TTCTATCTATACCCT[C/T]GAAGAGCTGTCTCTG | 79658 |
| rs79780617 | snp | A/C | 0.0908922 | 0.192833 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147845317 | CTTATATATCTCCTT[A/C]GGTGTTCATGTATCT | 79658 |
| rs79789847 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147830952 | AATATGCTATTCTTT[C/T]TTTAGTATGCCCTAG | 79658 |
| rs79798576 | snp | G/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148010115 | CCTCCACTTTTTTTT[G/T]GTCATGAGGTTGGAG | 79658 |
| rs79806464 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148055933 | TTGTCTTCATCTCCC[A/C]CAAACCCCACGTCCC | 79658 |
| rs79823199 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148046581 | TTCTTGATTTCATTG[G/T]TTTATACCTGGACTC | 79658 |
| rs79830436 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148045183 | CAGAATGTTCTGCAC[A/G]GTGTCCTCCAGGGGT | 79658 |
| rs79841688 | snp | A/G | 0.067446 | 0.170804 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147957199 | TTGCACCTAAGTGCC[A/G]TTGTGGTTGGAATGG | 79658 |
| rs79848599 | snp | C/G | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148003894 | GTCTTTTATCTGAGT[C/G]TAAGCCTAAATCAGC | 79658 |
| rs79881963 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148043040 | TCCCAAGACCAAGAC[A/G]TGGTCTGCACCCTGA | 79658 |
| rs79888265 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147836208 | GATACTAAGAGAATC[A/G]TAGACTTTGGTGATA | 79658 |
| rs79893746 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147814576 | CTCCCACATGTGGGA[A/G]TGTTTTTCTTTTGGT | 79658 |
| rs79904962 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147752542 | ACTCACAGTTTGATC[C/T]TTTTTTTTTTTTTGG | 79658 |
| rs79929689 | in-del | -/TTTTTTTG | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147830529 | TTTTTTTTTTTTTTT[-/TTTTTTTG]ATGGGGGGAGCCTTG | 79658 |
| rs79937933 | in-del | -/ACA | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147900843 | ACAACAACAACAACA[-/ACA]CGCCTTGAGACAGGT | 79658 |
| rs79952475 | snp | A/G | 0.0926964 | 0.194308 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147836183 | CTAACATACTTGTTC[A/G]TAGAAGATAGATACT | 79658 |
| rs79953824 | snp | C/G/T | 0.444444 | 0.157135 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147839093 | TGTTTAGATCTATCG[C/G/T]ATCTATCTATCTATC | 79658 |
| rs79958772 | snp | G/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147736487 | GGTTTCCTTTTTTTT[G/T]GTAAAATGGGACTGA | 79658 |
| rs79961279 | snp | A/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147818583 | AAAAAAAAAAAAAAA[A/T]AAGTTAGTTTGTTAG | 79658 |
| rs79964283 | snp | A/G | 0.152001 | 0.229992 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147846357 | CTTAAATAGTGTTTC[A/G]AGATTTTCTTTTCTA | 79658 |
| rs79966540 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889457 | GGCATACACCGCCAC[A/G]CCCGGCTAATTTTTG | 79658 |
| rs79992885 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147919577 | AAACAATTTTTTTTT[C/T]TTTTTTTTTTGTGGA | 79658 |
| rs80003949 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148047602 | AGGACAAATAATATT[A/G]ATACAAATAAAGTAC | 79658 |
| rs80026408 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147993387 | TTATATTATTCTTTT[C/T]CCTTACATTTATGTC | 79658 |
| rs80034292 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147876086 | ACATGACTCAGGGAA[C/T]GGTTACAGGGTATCT | 79658 |
| rs80044485 | snp | A/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147784145 | ATTGTGTATTATATA[A/T]TTTACATAACATTAA | 79658 |
| rs80046286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148027836 | AAGCAGGCCACTGTG[C/T]GGTCTTTTTAAATGT | 79658 |
| rs80048164 | snp | A/C | 0.00557542 | 0.0525036 | upstream-variant-2KB | ARHGAP10 | GRCh38.p7 | 4:147731310 | GCGGTGAAAACCACA[A/C]GTTACCTGGCATGTT | 79658 |
| rs80049072 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147769459 | CATTAAAAATTGTGC[A/G]TCAAGGATTTTATTT | 79658 |
| rs80057641 | snp | C/T | 0.0923359 | 0.194016 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147830322 | CGGTCACAGGCAAGA[C/T]GTGATGCCTGCTCTC | 79658 |
| rs80059293 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147835916 | GAGGTTCTTACTGTC[C/T]CTTATGCACAGAGGG | 79658 |
| rs80074790 | snp | C/T | 0.0498117 | 0.149749 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147815270 | TGTGTCTGTGTCCTC[C/T]TCTGTTGTAGTGATA | 79658 |
| rs80107847 | snp | C/T | 0.277778 | 0.248452 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147978623 | CTTTCCCTTCACCTT[C/T]CACCATGACTGTAAG | 79658 |
| rs80116261 | snp | C/G | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147991086 | AAATAACCTTTACAC[C/G]AAACCCCCGTGACAC | 79658 |
| rs80132475 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148044956 | GGAAAAAGTGGCTTC[A/G]CTGAAAGAGCAATCA | 79658 |
| rs80136345 | snp | G/T | 0.0984431 | 0.198823 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148070742 | TGAAATTATTCTCCT[G/T]GGTTGTGATCAGAAG | 79658 |
| rs80146386 | snp | G/T | 0.109461 | 0.206758 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147779221 | GAGCATGTAAGCTGC[G/T]GCCAGAGGAGTCATG | 79658 |
| rs80148116 | snp | A/C | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147739189 | GAGACTCTGTCTCAA[A/C]AAAAAAAAAAAAAAG | 79658 |
| rs80155417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147780415 | AAGGGTGAAACAAAA[C/T]GGTACCATAGTGGAG | 79658 |
| rs80175110 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147915628 | ATAAGTATATAGATG[C/T]TGAATAGGTCTACAC | 79658 |
| rs80184160 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147874365 | TGTTTTCGGTGTAGC[C/G]GTTTGACAGATATTG | 79658 |
| rs80201109 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147952366 | ATGTATTTCTTTACA[C/T]CCTCACCAACAATAT | 79658 |
| rs80211380 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147831012 | TCCAGCATCACTTTA[A/G]GAACGTGCAAGAAAT | 79658 |
| rs80226866 | snp | C/G | 0.0279526 | 0.114869 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147810842 | CCATCATGACAGGGT[C/G]TGTCACTTCATTAAC | 79658 |
| rs80227779 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147857031 | CTAACTTTTGTATTT[G/T]TAGTAGGGACGGGAT | 79658 |
| rs80271450 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147877565 | ATGTTAATTGCTTTT[C/T]TAAAAGTGTCTTGAC | 79658 |
| rs80279499 | snp | A/G | 0.093417 | 0.194889 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147988355 | AATTTCATTTACTAG[A/G]TCATGTTTTCTGAGA | 79658 |
| rs80305223 | snp | C/G | 0.021333 | 0.101051 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147844479 | CATCCCTACCTCCCC[C/G]CTACTATACTTCCCA | 79658 |
| rs80315009 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147945432 | AACACATAATTACAC[A/G]CTATTTGGATAAAGA | 79658 |
| rs80344637 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147928103 | CAGTCCATTTTGACC[A/G]TAATACAGAGGTTAC | 79658 |
| rs80356295 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148035523 | TCTAGCAACTGACTG[C/T]CATTCATCTGTACAT | 79658 |
| rs111216524 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147784264 | ATTAAATTGTGTATT[A/T]TATAATTTACATAAC | 79658 |
| rs111274014 | snp | G/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147961719 | ATTTTAGTAGAAAGG[G/T]GCTCTCAGTTGATAA | 79658 |
| rs111286686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147895389 | ACAAAAACAGCCTTA[A/G]GGCCAGGCATGGTGG | 79658 |
| rs111297537 | in-del | -/A | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147895699 | GAGAGACCCTGTCTC[-/A]AAAAAAAAAAAAAGA | 79658 |
| rs111300055 | snp | C/G | 0.0197687 | 0.0974348 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147896253 | GTTTTCCCTTCTTCA[C/G]TGTTTTTTCATAAAT | 79658 |
| rs111306626 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147936462 | GCCTCCCGAGTAGCT[C/G]GGACTACAGGCGCCC | 79658 |
| rs111315044 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147750182 | GTCAACACAGTTTCT[C/T]GGTTTAATGTATGCA | 79658 |
| rs111325310 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147808771 | AACTCTGGGCCCCCT[C/G]TGGTTCTGCACTCTT | 79658 |
| rs111326167 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148001345 | TTTGAAGTCAGGTAG[C/T]GTGATGCCTCCAGCT | 79658 |
| rs111348284 | snp | A/G | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147962898 | ACTCCTGACCTCAAG[A/G]GATCTGCCTGCCTCG | 79658 |
| rs111368634 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148041981 | TTCAACTCTCTGTGC[A/G]TGACTTTCAGATCAA | 79658 |
| rs111379548 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147921062 | AGTCATGCATGGGAT[A/G]CCCCAGGGTTCTGCT | 79658 |
| rs111387593 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147839126 | TCTATCTATCTATCT[A/G]TCTATCTATCTATCT | 79658 |
| rs111390651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148070930 | GTGAGGAGTGCTTGG[A/G]CCTGTGCCCTTTGCT | 79658 |
| rs111397229 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147837151 | TAAACTTGAGCCTAG[A/C]ATGATGGGGAAGGTA | 79658 |
| rs111407604 | snp | A/G | 0.14933 | 0.228835 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147850639 | GAAGGGACAAACTCC[A/G]GACACACCATCTTTA | 79658 |
| rs111411181 | snp | A/G | 0.021333 | 0.101051 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147757109 | ATATAAATCAAAGAT[A/G]ATAATCTTTTCAGCT | 79658 |
| rs111415098 | in-del | -/ATTAA | 0.439918 | 0.162576 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147771496 | ATTTTAAAATGTATG[-/ATTAA]ATTATTTTTGACTAT | 79658 |
| rs111417179 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148041348 | TTTCAGGGGGGAACT[A/G]TCTCTGACGTAACTG | 79658 |
| rs111426389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147764979 | AGTAGGAGCTGCTTT[C/T]CCACAAAAATGCCCA | 79658 |
| rs111427464 | snp | A/G | 0.095934 | 0.196885 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148017682 | TATATATATATATAT[A/G]TGTGTGTGTATGTAA | 79658 |
| rs111445094 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148005864 | CATTTACATGTTGAA[C/G]TTACTTTGGGAATGA | 79658 |
| rs111451451 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147892594 | TGTGGGGTTGGCTGG[A/G]AGTGTGGGGTTGGCT | 79658 |
| rs111453742 | in-del | -/G | 0.0818113 | 0.184966 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147877764 | TTCAGAGAGTGTTCT[-/G]GGGGCATACTTGGAC | 79658 |
| rs111472639 | snp | C/G | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147746543 | GTAGCTCGCTTGCCA[C/G]CACTCCCCGTTAATT | 79658 |
| rs111479139 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147846332 | TTTCTAAAAAGAGGG[A/C]TGGCACATTCTTAAA | 79658 |
| rs111480139 | snp | G/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147874847 | GCTATTTTTTTTTCT[G/T]TGCACATGAATCTCA | 79658 |
| rs111491090 | snp | G/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147920804 | GACTGTCTTTAGGAG[G/T]AGGCTTCCTCAGATT | 79658 |
| rs111491837 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147936482 | TACAGGCGCCCGCCA[C/T]CGTGCCCGGCTAATT | 79658 |
| rs111493889 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147833825 | TATTAAGTTGGTGGT[A/G]GAGATTGTGTTAGAT | 79658 |
| rs111500152 | snp | A/G | 0.0599851 | 0.162463 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147856704 | CCAAAATTCAAAAAT[A/G]TCCAAAAATCTCTAC | 79658 |
| rs111506471 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148008123 | TTTTGCATTGCTCCT[C/T]CTGAGGCATACAGTC | 79658 |
| rs111508049 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147794363 | CAACATAATGTTAAT[G/T]CTCACAACATTCCTA | 79658 |
| rs111519412 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147909207 | AACTCTGCAAGGGCC[C/T]AGTGGAAGAGATGCA | 79658 |
| rs111520799 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147783941 | ATTATATTTATATAA[C/T]ACACATTAAATTGTG | 79658 |
| rs111525874 | snp | A/C | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147918335 | AGAGACAGGGTTTCA[A/C]CGTGTTAGCCAGGAT | 79658 |
| rs111543831 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147887841 | CACTCCAGCCTGGGC[A/G]ACAGAGCGAGACTCC | 79658 |
| rs111545632 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147903334 | ATAGTTTTCAGTTCA[C/T]AGTCAGAAGAGGAAG | 79658 |
| rs111548830 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148058409 | ATGCGTATTCTCCTC[A/G]CTCTACCCTTTTGAA | 79658 |
| rs111560424 | in-del | -/A/AA/AAA | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147882462 | GTGAGACTCCGTTTC[-/A/AA/AAA]CAAAAAAAAAAAAAA | 79658 |
| rs111575300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147890713 | GTGCCTATAATCCCA[A/G]CTACTCGGGAGGCTG | 79658 |
| rs111586597 | snp | C/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147985501 | TACAGCGACTCTCCT[C/T]TTACTTTTGGACCTG | 79658 |
| rs111625866 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147917248 | AGCAGAAGAGCCACA[A/G]TGAACCTCCCCCATC | 79658 |
| rs111627385 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147931003 | TTTCTGGAGCTGTGT[A/G]GTCTCTGGCTCTGGT | 79658 |
| rs111628953 | snp | G/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147947948 | ACCTGCCACTGTTTT[G/T]TTTTTTTTTTTGAGA | 79658 |
| rs111634876 | snp | A/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147934335 | AGTGACCCTCCCAGG[A/T]CTTGGGCTCCACCAA | 79658 |
| rs111648154 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148060909 | GTGGAGAACTTGACC[C/G]TGGACAAGGACTGCT | 79658 |
| rs111656717 | snp | C/G | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147791266 | ACAAGCGCCTGCCAC[C/G]ATGTCTGGCTAATTT | 79658 |
| rs111661673 | snp | A/G/T | 0.0330092 | 0.124309 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147969780 | CAGCAGACGAAAGTG[A/G/T]CCTCGCTTTCAGAGC | 79658 |
| rs111677127 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147983767 | TTGCATTTCTTTGCT[A/G]TCCATATCCTGGATT | 79658 |
| rs111678766 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147792998 | CAAAAATTAGCTGGG[C/T]GTGGTGATGCATGCC | 79658 |
| rs111680260 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148007422 | GATGGAGGAAGAAGA[A/G]TGTGACAGGTCAGCT | 79658 |
| rs111687347 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148005054 | AAAGAATCTCATGCC[A/G]CTTGCTGATCCAACT | 79658 |
| rs111690062 | snp | A/C | 0.0644693 | 0.167566 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147758991 | AAAAAAAAAAAAAAA[A/C]CCGAAAACAGGTGGT | 79658 |
| rs111694555 | in-del | -/TT | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147752541 | ACTCACAGTTTGATC[-/TT]TTTTTTTTTTTTTTG | 79658 |
| rs111696530 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147970927 | ACCCCATCTCTACTT[A/G]AAAGAAAGTACAAGA | 79658 |
| rs111710828 | snp | A/C | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147739584 | CACAATAAAAGAAGA[A/C]GACCAGAGACATCCC | 79658 |
| rs111714288 | snp | C/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147859623 | ACTGTGCATTTGTTA[C/T]GTGGCTTCTTCCACT | 79658 |
| rs111716507 | in-del | -/C | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148023849 | ACTTGCCCCATTTTT[-/C]TGACTTGTTCATCAG | 79658 |
| rs111730885 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147810706 | AGACCTCTCTGTAGT[G/T]CCTTAGGGTATGGTG | 79658 |
| rs111735804 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148034030 | TGATGTTGTTTATGA[C/T]CTCAGCAAATCTCTC | 79658 |
| rs111739701 | snp | A/G | 0.0807149 | 0.183963 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147878243 | TGGGACTACAGGCGC[A/G]TGCCACCACGCCTGG | 79658 |
| rs111740200 | snp | A/G | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147839138 | TCTATCTATCTATCT[A/G]TCTATCTGTCTGTCT | 79658 |
| rs111753472 | snp | C/T | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148072390 | AGGGCAGCCTTCTGC[C/T]ACCTGTGTCGCCTCC | 79658 |
| rs111758119 | snp | A/G | 0.259397 | 0.249823 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148002918 | tctctatctccttca[A/G]ttctgctctgatctt | 79658 |
| rs111761449 | snp | A/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147999804 | AGCTCTGGGGCAAGG[A/T]CCCCTGCCCTGCCCC | 79658 |
| rs111768407 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147826064 | TGGAGTGGTGAGGTG[C/T]GGACTGCCTTTTCAG | 79658 |
| rs111771375 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148025263 | GCTACTTAACTTCTT[C/T]AGTCTGGTTTTTATG | 79658 |
| rs111777276 | snp | A/C | 0.0283406 | 0.115616 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147792357 | GAGCTGCCTATTTAT[A/C]ACATGTCCTCTTCCT | 79658 |
| rs111782587 | snp | G/T | 0.0325976 | 0.123435 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147953034 | AATTGTCTATTGATA[G/T]GATCATACAGTTTTC | 79658 |
| rs111784477 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147746571 | ATTTTTGTATTTTTA[A/G]TAGAGACGGGGTTTC | 79658 |
| rs111808390 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147757699 | CAGCTTCACCTTCCA[C/T]GACTGCACACCTGGG | 79658 |
| rs111811844 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147866910 | TTAAATGAAGACAAT[A/G]CTGATCTGTTTGTAC | 79658 |
| rs111818514 | snp | A/G | 0.0652144 | 0.168387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147830006 | AGATGGAGCTGTTCC[A/G]CCTCCCTCTCATCCT | 79658 |
| rs111821789 | snp | C/G | 0.259397 | 0.249823 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148000033 | CTGCACCTATTAACT[C/G]GTCATTTACATTAGG | 79658 |
| rs111823428 | snp | A/G | 0.0558544 | 0.157504 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148066702 | TTTGCCTGGGCTCAC[A/G]CCATGGCTTTCTTAT | 79658 |
| rs111825022 | in-del | -/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147973148 | GATATTCAGTGTCAA[-/T]TTTTTTTTGTTGTTT | 79658 |
| rs111845236 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147960735 | CCCTTTCTCTTGCTC[A/T]TGTGGTCATTATCCA | 79658 |
| rs111866164 | in-del | -/G | 0.0182019 | 0.0936463 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148067766 | CGTCAGTAGTTATGC[-/G]GTTTGGGATGTGTGC | 79658 |
| rs111872757 | in-del | -/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148048959 | AGCCTGGAAAGGAGA[-/T]TTTTTTTTTTTTTTT | 79658 |
| rs111931638 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147997228 | AATACCCAGTGTGGA[A/G]TCTACAAACGTATTG | 79658 |
| rs111943375 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147803309 | CCACTGCATCCAGCC[C/T]ATTTATTTTTCTTTT | 79658 |
| rs111947662 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147958254 | AGTGGACTCATGCCT[A/C/T]AGGGTTGGAGTCATG | 79658 |
| rs111948960 | snp | A/C | 0.0189856 | 0.0955633 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147982260 | TCTGTAGCTACCTTT[A/C]AGATTTTTTCTTTTG | 79658 |
| rs111948971 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148001009 | CCTTGCCCATGCCTA[C/T]GTCCTGAATGGTATT | 79658 |
| rs111955874 | snp | A/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148036949 | GAAACAAGGCTGTTC[A/T]GTTTTCTTCAAAAAC | 79658 |
| rs111966522 | snp | C/T | 0.0513262 | 0.151752 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147849753 | GGTGGTTTTTGTAAA[C/T]TGGATTTTGAAAAGC | 79658 |
| rs111974112 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147795555 | AACGCAACTTCTGGA[A/G]TGTGAGCTCTTTGAA | 79658 |
| rs111974847 | in-del | -/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147803015 | AGTTTTGTTTATTGC[-/T]TTTTTTTTTTTGAGA | 79658 |
| rs111979085 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148031893 | TTTATTTCAGTGATA[C/T]TAAGTACTGCAAAAG | 79658 |
| rs111982195 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147743057 | TTTTTATTTTTGGAG[A/G]CAGTCTCACTCTGTC | 79658 |
| rs111997154 | snp | C/G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147906057 | TTGTGTATAAGAATG[C/G/T]TTGTGATTTTTGTAC | 79658 |
| rs112008373 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147838545 | TGATTTCTCTTCCTC[C/T]TCTTCTTCTTCACAG | 79658 |
| rs112013145 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911560 | GTAGAGACGGGGTTT[A/C]ACCGTGTTAGCCAGG | 79658 |
| rs112022317 | snp | C/G | 0.0260105 | 0.111035 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147877177 | GGCATTTGGGCTAAG[C/G]TTAAATTTTTTTTGG | 79658 |
| rs112022889 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147836240 | ATTGACCTTTTTTTT[A/T]ATTTTTATTTTTTGA | 79658 |
| rs112034189 | snp | C/G | 0.5 | 0 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148023407 | CTTTGTCTGGAGCTG[C/G]AAGATGGTAAGATGT | 79658 |
| rs112034820 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147854228 | TTGGCTTCCTCGTGT[C/T]GTTACAATTAAGAAA | 79658 |
| rs112036473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148057286 | GCGTACAATCCTTCA[A/G]TGGCCCCTCTTTGCC | 79658 |
| rs112036582 | snp | A/G | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147750183 | TCAACACAGTTTCTC[A/G]GTTTAATGTATGCAG | 79658 |
| rs112041240 | snp | C/G | 0.0217236 | 0.101931 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147786965 | GGATGCTTTTCATTT[C/G]TTATCTCCACCTCTT | 79658 |
| rs112042453 | snp | C/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148039336 | TCTCTGCTCAAATTT[C/T]TTTTCTTTAATACTT | 79658 |
| rs112053107 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147741055 | TTTGTGAGATTCATC[C/T]AATTGGATGTATGTA | 79658 |
| rs112075667 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148046167 | TGAGCTCTCTTGTCC[A/G]TCTTCTGCATTTTCT | 79658 |
| rs112077895 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147789414 | TGAGCTTCAGCCTCC[C/T]GGGTAGCTCGTATTA | 79658 |
| rs112078795 | snp | C/T | 0.039522 | 0.134904 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147970425 | TACAGTAATGGATGG[C/T]GGTGGGGGGAGGGTG | 79658 |
| rs112079056 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147957166 | AATACTGTTTCTACT[A/G]TAATCATTGGCATGG | 79658 |
| rs112083188 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148069024 | TGACAGACACTGAGA[C/T]TGCCATGTTCTCCAC | 79658 |
| rs112090958 | in-del | -/GT | 0.0279526 | 0.114869 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147985089 | AATCTCATCCAGGAG[-/GT]AGTGGGTCCTCCAGG | 79658 |
| rs112095776 | in-del | -/CA | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147741793 | ACACACACACACACG[-/CA]CACACACACACACAC | 79658 |
| rs112106940 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147947888 | TCTATTATCCTGCTT[C/T]TTGAGTTATCAACAT | 79658 |
| rs112125052 | in-del | -/A | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148056492 | GTTTAAGGTATGCAG[-/A]AAAGTTACAAAGATA | 79658 |
| rs112134436 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148007901 | CCCGGTCACAGTCTT[C/T]GGAGACACTTCCGTT | 79658 |
| rs112137290 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147765125 | GATGGACCATGTTGG[A/G]CAGGGAAATGGGGAA | 79658 |
| rs112137798 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147811279 | CTTCTAGTAGCTCCT[C/T]GTTGGAATACTGGCC | 79658 |
| rs112144037 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147852828 | AGTTCAAGTGATTCT[C/T]GTGCCTCAGCCTCCC | 79658 |
| rs112146231 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147972634 | GTCAGTGCTAGTGTC[A/G]GGGTTGTCTAGGGCC | 79658 |
| rs112152798 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147996055 | CTTGACCTTCCACAG[A/G]GGGCCTGTATGTGTG | 79658 |
| rs112177385 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147930408 | TATATACCATAGGCT[A/G]AGGACAAGTTGAGGT | 79658 |
| rs112184235 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147933153 | TCTTCATCACTTTAG[A/G]GTTGGTCTCTGGTGC | 79658 |
| rs112200123 | snp | A/C/T | 0.0425829 | 0.139564 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147898344 | TTCATTGTCTTCAGG[A/C/T]TTCCGTTTATTTTCT | 79658 |
| rs112205820 | in-del | -/AGTC | 0.00636936 | 0.0560724 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147948315 | AAGTCATTTTTAAAA[-/AGTC]AGTCAAAATATAATT | 79658 |
| rs112217318 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147815619 | CCCAGCACTTTGGAG[G/T]GCCAAGGCAGGGGGA | 79658 |
| rs112218084 | snp | G/T | 0.0341408 | 0.126114 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148036594 | CCTTCTGCCATGATT[G/T]TAAGTTTCCTGAGGC | 79658 |
| rs112230555 | snp | A/C | 0.0414363 | 0.137845 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147987428 | ACTTCCTCTTTTTAC[A/C]TTTTTCTGGGTCCCT | 79658 |
| rs112235378 | snp | A/G | 0.259397 | 0.249823 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148000208 | TTGCGATAGTTTGCT[A/G]AGAAGGATGGTTTCC | 79658 |
| rs112245819 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147865622 | ATTCATTTTAATTTT[A/G]ATATCGACTTATTGA | 79658 |
| rs112261387 | snp | C/T | 0.0700422 | 0.173537 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147931781 | GCAAAGATTTCATGA[C/T]GAAGATGCCAAAAGC | 79658 |
| rs112274858 | snp | A/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147864061 | AAATGCCCAGATAAA[A/T]ATTTTTAAGAGTAAA | 79658 |
| rs112292756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148020980 | AGCTGTAGAATACCT[A/G]TATCTAAATCACTGT | 79658 |
| rs112298617 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147790142 | AGGTGCTGGTATATT[C/T]GGTATCTGGTGAGGG | 79658 |
| rs112306254 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147790495 | TACTCTCAAATATTC[C/T]AAGATGTAACAAAAC | 79658 |
| rs112306845 | snp | A/G | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148006449 | CCTGACCCCAGCAGC[A/G]TCTGATCATTGTTGC | 79658 |
| rs112312087 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147825448 | CGAGACTCCATCTCA[A/G]AAAAAAAAAAGTGAC | 79658 |
| rs112319767 | snp | C/G | 0.0803491 | 0.183626 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147997741 | AAGATTAATTCTGAG[C/G]TTGATAAGTCTTGAG | 79658 |
| rs112320752 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147791535 | CCGTGTGTGTGTGTG[C/T]GCGCGCGTGCGTGCG | 79658 |
| rs112322419 | snp | A/C | 0.0490535 | 0.14873 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147969791 | AGTGGCCTCGCTTTC[A/C]GAGCTTTATAGAGCT | 79658 |
| rs112328285 | snp | C/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147985966 | GTTTGCCCACCTTCT[C/T]CTCTCTGGAGTCTGG | 79658 |
| rs112329446 | in-del | -/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147795701 | TTTAATTTAATTTAA[-/T]TTTTTTTTTTTTGGA | 79658 |
| rs112330362 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147906039 | GCTCTCTTTGTCTAT[A/T]ATTTGTGTATAAGAA | 79658 |
| rs112338731 | snp | A/T | 0.0256215 | 0.110247 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147880396 | ACAGACATGGAAAAT[A/T]AGTCATGGTGAGGAG | 79658 |
| rs112374126 | snp | A/G/T | 0.0276236 | 0.114613 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147892688 | GAGACTCAGAGGAAG[A/G/T]GGGGCCCAAGGCAAA | 79658 |
| rs112379304 | in-del | -/A | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147887861 | GCGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAT | 79658 |
| rs112381182 | in-del | -/AC | 0.375 | 0.216506 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148063843 | CCTTTCCATGAACGG[-/AC]ACAGAGGTTGCTTTA | 79658 |
| rs112387712 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147834226 | TGTAGTCCCAGCACT[C/T]TGGGAGGTGAGGCAC | 79658 |
| rs112394510 | snp | A/G | 0.0535932 | 0.154675 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147839130 | TCTATCTATCTATCT[A/G]TCTATCTATCTATCT | 79658 |
| rs112396444 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147832290 | ATTAGATGGTATAGC[C/T]TTGAAAACAAAGAAC | 79658 |
| rs112398833 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148060922 | CCCTGGACAAGGACT[A/G]CTGATTCTGTGTTCC | 79658 |
| rs112409497 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147934351 | CTTGGGCTCCACCAA[A/G]GTTTCACAAACTTTT | 79658 |
| rs112437024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147747251 | ACAGGGAATAAAATG[C/T]CTCTGGCAGCACCTG | 79658 |
| rs112437404 | in-del | -/AAAAC | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147860435 | GACAGCTCCGTCTCA[-/AAAAC]AAAACAAAACAAAAC | 79658 |
| rs112443466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147874824 | ACTCCTCTGGTAGCT[A/G]TTTTACTGCTATTTT | 79658 |
| rs112446150 | snp | C/G | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147740137 | CACTGCAACCTCCGC[C/G]TCCCAGGTTCAAGCA | 79658 |
| rs112446557 | in-del | -/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147961620 | TTTCCCATTCTCTTG[-/T]TTTTTTTTTGCTTTC | 79658 |
| rs112447408 | snp | A/G | 0.021333 | 0.101051 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147864577 | GAGTAGGAGTCACAA[A/G]CTTTTTCTGCAAAGA | 79658 |
| rs112452844 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147895562 | TGGTGGTATGTGCCT[A/G]TAGTCCCAGCTACTC | 79658 |
| rs112465142 | snp | C/G | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147984189 | AGATGGCGCTTAAGA[C/G]TAATAGCTGCCTGGG | 79658 |
| rs112468228 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147997265 | GAGGGAAAAATGTAA[A/G]CTGTACATCAATAAT | 79658 |
| rs112471621 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148007463 | GCTCAGTAGCGAGAA[A/G]TATGAGTCACTTGGC | 79658 |
| rs112487867 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148010302 | GTTACTCTTTCAAGA[C/T]CACAGTGCATTTAAA | 79658 |
| rs112492537 | in-del | -/A | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148055064 | AAGTTCAGCCCTCTT[-/A]ACCTGATTCCACACT | 79658 |
| rs112496106 | snp | C/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147757740 | GTTCTTCAGTCACCT[C/T]CCTAAGAGAATCTGG | 79658 |
| rs112499570 | snp | C/T | 0.0652144 | 0.168387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147902633 | TGTAGTCCCAGTTAC[C/T]CAGAGGCTGAGGTAG | 79658 |
| rs112501991 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147918311 | TGGCTAATTTTTTGT[A/G]TTTTTAGTAGAGACA | 79658 |
| rs112502143 | snp | C/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147952352 | TTCTTCCCAAGTTGA[C/T]GTATTTCTTTACATC | 79658 |
| rs112525769 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147801818 | CTCCATGAAGCTTTT[C/T]TTCCTCTGCTGCAGA | 79658 |
| rs112527094 | snp | A/T | 0.0429648 | 0.14013 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147888764 | AATTTCCTGCCATTT[A/T]CCACCGTCTGTGTCT | 79658 |
| rs112532261 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889970 | TGATATAATCCTGCT[C/T]TCTCGAGCATAGTTT | 79658 |
| rs112535700 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147924412 | TTTCCTCCTCTTTAA[C/T]GCATCCACAGAATAG | 79658 |
| rs112537830 | snp | A/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148048974 | TTTTTTTTTTTTTTT[A/T]AATGGAGACTTTCTT | 79658 |
| rs112549062 | snp | C/T | 0.26271 | 0.249677 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148003110 | agagattctggtatg[C/T]tgtgtcgttgttctc | 79658 |
| rs112553527 | in-del | -/AGGGGCGTGA | 0.0221141 | 0.102801 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147981945 | CTTTACTTTGAGCCC[-/AGGGGCGTGA]TCATATGTGAGATGG | 79658 |
| rs112562846 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148004365 | ACATTCTGTAGCCTT[C/T]TGAAAAGAATGAATA | 79658 |
| rs112577449 | snp | C/G | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147996078 | TATGTGTGAAATACT[C/G]AAAAAGCTCTTCTTT | 79658 |
| rs112579754 | snp | G/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147954520 | GCATCTTTGATTTTT[G/T]TTTTAAACATTTGAA | 79658 |
| rs112610876 | snp | A/G | 0.021333 | 0.101051 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147758107 | GTCCATACTGAAAAT[A/G]CAAAAATTAGCTGGG | 79658 |
| rs112615534 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148028888 | AAGTGGACATTATTC[A/G]CCACAGATTAGGCTC | 79658 |
| rs112619394 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147851621 | TTACATTGTATTTAA[C/T]AGAGCAGAAACAATA | 79658 |
| rs112624537 | snp | G/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148068168 | CCAGTTAGATGGGCA[G/T]TGGTTGCCTCCTCAG | 79658 |
| rs112625871 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147799223 | TATTTTTAGTAGAGA[C/T]GGGATGGGGTTTTGC | 79658 |
| rs112627249 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148059521 | GAAAGGACTCTCAAA[A/T]ATTTCATTATGTTCT | 79658 |
| rs112638787 | snp | A/G | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147997606 | CATCAGAAGGCATCA[A/G]CACAGGTATAGAACC | 79658 |
| rs112639052 | snp | G/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147796384 | TTTAAAAGCGTAGTG[G/T]AAGGAGACACCTGGG | 79658 |
| rs112661658 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147923858 | GTATGGAAAGGAAGA[G/T]GTCCAGAGTGAACCT | 79658 |
| rs112670624 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147962331 | ATAGTAACACGAACA[A/G]CAACAGTACTAATGG | 79658 |
| rs112671207 | snp | A/C | 0.0197687 | 0.0974348 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147895929 | TTTATTCCCAGTTTT[A/C]AGCATGAATTGGTTG | 79658 |
| rs112682149 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147864441 | GATTTGTTCATCGAA[A/G]TGTTTGTTGATTGTG | 79658 |
| rs112704093 | snp | A/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147749497 | TGGATTGAATAATTT[A/T]ACATTCTTTTTACCT | 79658 |
| rs112704546 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147880856 | CAATTTTTATAGGCC[A/G]AAAATAGTCACATAT | 79658 |
| rs112707617 | in-del | -/ACACA | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147920262 | CTCTACCAAAAATAC[-/ACACA]AAAAATTAGCTGGGC | 79658 |
| rs112735856 | snp | A/C | 0.0174175 | 0.0916809 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147926168 | CATTGTCTGCCTTAA[A/C]TCTTTCTGTAGGCTG | 79658 |
| rs112757025 | in-del | -/TTT | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148005701 | TGAATCTGATTCTTC[-/TTT]GAGTTTGTACACCTT | 79658 |
| rs112761699 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147930022 | AATCCTGTGAATGCC[A/G]GTATGAACATTAATG | 79658 |
| rs112764350 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147757302 | CGTGTTCAAGCAATT[C/T]CCCTGCCTCAGCCTC | 79658 |
| rs112779458 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148050620 | CCTCGTGATCCACCC[A/G]CCTCGGCCTCCCAAA | 79658 |
| rs112782214 | snp | C/T | 0.021333 | 0.101051 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147869236 | GCCCTGAAGCCAGCT[C/T]TCTGCCTCAGACTCT | 79658 |
| rs112789914 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147793125 | AGCCTGGGCGACAGA[A/G]TGAGACTCTCTGGAA | 79658 |
| rs112796746 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148004664 | GTCAGCAAAAGCCAC[A/G]GCCTTTAGTCCTGCA | 79658 |
| rs112811590 | in-del | -/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147983188 | TGCCTGGCTGCTTTG[-/T]TTTTTTTTTTTTTTT | 79658 |
| rs112820247 | snp | A/G | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147765610 | TTCGAGACAGGCCTG[A/G]CCAACATGGTCAAAG | 79658 |
| rs112832767 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147985055 | TCTCAAGTTCTCTGC[A/G]TGAGGCAGTGGAGCT | 79658 |
| rs112860150 | in-del | -/C | 0.335559 | 0.234904 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147925431 | GTTTGAGTCTCTTTT[-/C]TGATTTATTGTAGTA | 79658 |
| rs112863377 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147936186 | CTTCTGGCTTCCAAA[A/G]AGAAGGAAGGATTGA | 79658 |
| rs112863885 | snp | A/G | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148005557 | AATGGCTATTAAAAT[A/G]TATATTAAAAAACAA | 79658 |
| rs112871914 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148053872 | TGCCTTCCTTTGCTG[G/T]GCTGTAGCTGCAGGT | 79658 |
| rs112882740 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147793895 | ATCTAAAGTTCCACC[C/T]GCAAAGTAGGTTCAG | 79658 |
| rs112886024 | snp | C/G | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148036948 | AGAAACAAGGCTGTT[C/G]AGTTTTCTTCAAAAA | 79658 |
| rs112893064 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148060472 | TTACACGACTTAAGT[A/C]TATTTACTCACTTGC | 79658 |
| rs112893945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147969771 | CAATAGTTACAGCAG[A/G]CGAAAGTGGCCTCGC | 79658 |
| rs112903591 | snp | A/G | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148002165 | TTTTGCATCTATTGA[A/G]ATAATCATGTGGTTT | 79658 |
| rs112904921 | snp | G/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147962052 | AGAACATTTCTAGCC[G/T]TGATCTCTAAAGCCT | 79658 |
| rs112908942 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148003890 | CAGTGTCTTTTATCT[A/G]AGTGTAAGCCTAAAT | 79658 |
| rs112911809 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147925266 | CATTCTTCCTCCTGG[G/T]ATTTAGTACCTGCTG | 79658 |
| rs112919783 | snp | C/G | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147978082 | GATGGGCACTCTATT[C/G]ATTCCATGTCTTTGT | 79658 |
| rs112931386 | snp | A/C | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147852996 | ACACTTTTAATATTA[A/C]ATATTGAAATAAATG | 79658 |
| rs112959028 | snp | C/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147859612 | CTGTTTGACAAACTG[C/T]GCATTTGTTACGTGG | 79658 |
| rs112959446 | snp | A/G/T | 0.0139034 | 0.0824216 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147926767 | AGAAGGATGGTTGTA[A/G/T]GGGAATCCATAAGAG | 79658 |
| rs112960686 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148050789 | TTATAAGTTCTCATT[A/G]TATGTTCTCTTCTTG | 79658 |
| rs112978746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147943071 | TTTTTAGTAAATGGA[A/G]TGAGAATGTAAAATA | 79658 |
| rs113010097 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147972177 | GGGTAGAAAGTATAA[C/T]GTAAGGTATAGTTAA | 79658 |
| rs113012026 | in-del | -/A | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147755546 | CAAAAAAAGGGAAAG[-/A]AAAAAAAAATACCAG | 79658 |
| rs113014263 | snp | C/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147880932 | GAGTACAATAAGAGA[C/T]TAACAGTATTCCAGT | 79658 |
| rs113021755 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148057158 | CAAAAAGAGGAACAA[A/G]CCTAGGGGAGGAAGA | 79658 |
| rs113021790 | in-del | -/TA/TATA | 0.00835141 | 0.0640778 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147791556 | GTGCGTGCGCGCGTG[-/TA/TATA]TATATATATATATTT | 79658 |
| rs113025381 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147862527 | CCCTGGCTGCACTTT[A/G]CCCTCTGCAGCTGGT | 79658 |
| rs113027493 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148005942 | AACAAATACATGTAT[A/C]TCTTAGTGCAGATTA | 79658 |
| rs113040696 | snp | C/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147757878 | ATCCCTGTCCAGTCA[C/T]CTGTGATACAGAACA | 79658 |
| rs113042079 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148001752 | TGCTTGTGATTTTTG[C/T]ACATCGATTTTGTAT | 79658 |
| rs113046490 | snp | A/C | 0.0364509 | 0.129988 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147974812 | GCTGGGGAGGCCTCA[A/C]AATCATGGCGGAAGG | 79658 |
| rs113059244 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147920364 | GGAGCTTGCAATGAG[C/T]GGATTGCGCCACTGC | 79658 |
| rs113060553 | snp | A/G | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147958008 | TTATAAAAGGAACCC[A/G]GTAGACGATCCATCT | 79658 |
| rs113066898 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147959981 | CTTTTTAATTTTTGC[A/G]ATATAAAATTCTTAT | 79658 |
| rs113081304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147944129 | TAAATAATTGATTTA[A/G]TGAGAGAGAGAATAT | 79658 |
| rs113091312 | snp | C/T | 0.103794 | 0.20279 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147893442 | ATATTTCAATATATA[C/T]ATTATTATTCTCTCT | 79658 |
| rs113092859 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147878440 | TCATCAGTAAGAGCA[A/G]CTGCTTACTAGGATG | 79658 |
| rs113098772 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148025246 | AAGGGAAAGGATTGT[C/T]AGCTACTTAACTTCT | 79658 |
| rs113101054 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148033789 | TGAGCTGGCCTGGAG[A/C]GACTTCATTGGCACT | 79658 |
| rs113115106 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148066418 | AATGAGGGTCAGTGC[A/C/T]TAAAGCCAATGCAGA | 79658 |
| rs113127539 | in-del | -/TTATTTAT | 0.0221141 | 0.102801 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147762499 | AAAAAAGATAATTGC[-/TTATTTAT]TTATTTATTTATTTA | 79658 |
| rs113136778 | snp | A/G | 0.259397 | 0.249823 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148000215 | AGTTTGCTGAGAAGG[A/G]TGGTTTCCAGCTTCA | 79658 |
| rs113140448 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147909614 | TCTTATTCTATCACA[C/T]TAACCAGAATCAAGC | 79658 |
| rs113148060 | snp | C/G | 0.0333695 | 0.124785 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147820793 | ATAGGGTTTCACCAT[C/G]TTGGCTGGGCTAGTC | 79658 |
| rs113150774 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147945520 | ATTTCCCGGATGACT[A/G]TATTATAGTGTTAAT | 79658 |
| rs113178826 | snp | A/G | 0.021333 | 0.101051 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147863345 | TGAGTGGGATCATAT[A/G]GTATCTGTCCCTTTG | 79658 |
| rs113188123 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147841873 | CACAACTACTACTAT[C/T]CTTGTTTTGGAAATT | 79658 |
| rs113189325 | snp | C/G | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147941355 | CTCATAAAATTCTAC[C/G]TGTACAGCATTGCTA | 79658 |
| rs113196414 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148065704 | ATGTGATGAATTTTT[A/G]TTTTGTGTGATTGGA | 79658 |
| rs113198835 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147856727 | ATCTCTACCACTTCT[A/G]GTTCTAAGCATTTCA | 79658 |
| rs113200979 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147869217 | GTGGACTGCATAGGT[A/G]AATGCCCTGAAGCCA | 79658 |
| rs113203146 | snp | C/G | 0.0287284 | 0.116357 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147837710 | GGGACCATCTCATTA[C/G]TGGAACCCTAGCTAG | 79658 |
| rs113207545 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148001560 | AGTATGGAATGTTCT[G/T]CCATTTGTTTGTGTC | 79658 |
| rs113218905 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147917666 | ATATTATCTTATTCT[A/G]GATTAGGTTGTATAT | 79658 |
| rs113219618 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147790427 | TGGGCTGTCTGGCAG[A/G]AAGTATGTTCTCAAT | 79658 |
| rs113223166 | snp | A/G | 0.279726 | 0.248226 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147912039 | TGTGTGTGTGTGTGT[A/G]TATAGTTTTCTTTAA | 79658 |
| rs113235801 | snp | C/G | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147903815 | GCACCGAATAATACT[C/G]CATTGTCAGGATGTA | 79658 |
| rs113243888 | snp | C/T | 0.077417 | 0.180873 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147752734 | GTTTTGCCATGTTGG[C/T]CAGGCTGGTCTCAAA | 79658 |
| rs113248980 | snp | C/G | 0.0429648 | 0.14013 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889987 | CTCGAGCATAGTTTA[C/G]TTTTATCAGTCACCT | 79658 |
| rs113261202 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147793307 | AATATAACACACACA[C/T]ATATATATATATATT | 79658 |
| rs113265930 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147747526 | CACCCTGACCGCCAT[A/G]GAGGTGGCCACACAG | 79658 |
| rs113267149 | snp | A/C | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147953532 | TGAGTTGTTGAATTT[A/C]TGGGCATAAAATTGC | 79658 |
| rs113273845 | in-del | -/GAACAA | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148063357 | CACAGGGGGCTTGAT[-/GAACAA]GAACCTGAGCAGGTT | 79658 |
| rs113276696 | in-del | -/A | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148054627 | TTGTTTTTAGCAGTT[-/A]ACTGTATTTATTCCC | 79658 |
| rs113279298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148067448 | GACAGACTGGCAGGT[C/T]ATCTGACCACGGCTT | 79658 |
| rs113307102 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147876421 | TACAGTGAAACCCTG[C/T]CTCTACTAAAAAATA | 79658 |
| rs113308054 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148037499 | CCACATTTGAGGAAA[C/T]AGTATGGTGCACTCT | 79658 |
| rs113309448 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147999271 | CCTGAGAGCACAGCA[A/G]GAGGGACAGTGATTG | 79658 |
| rs113312527 | snp | A/T | 0.0217236 | 0.101931 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147803796 | GAATAGTATTCCATT[A/T]TATCTATCTATAGAC | 79658 |
| rs113315519 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147927237 | AAGGGAAGTTGGGAG[A/G]GAAGATTTAAGTATC | 79658 |
| rs113326349 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147919822 | CTGACCTTAAGTATC[C/T]ACCCTCCTCTGCCTC | 79658 |
| rs113330172 | snp | A/C | 0.021333 | 0.101051 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147758133 | CTGGGCGTGGTAGCA[A/C]ATGCCTATAATCCTA | 79658 |
| rs113332867 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147869292 | TCTCTTGGGATGTTG[A/G]GTGAAACTCCTTGCA | 79658 |
| rs113345634 | snp | C/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147954709 | GCAAGGTGGACTGAA[C/T]TGTAGCATTTCTGTT | 79658 |
| rs113364763 | in-del | -/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147835791 | TCTCTTATGTAAAAC[-/T]AAAAAAAAAATTCAA | 79658 |
| rs113389469 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148048693 | AATATCACAGGCAGT[A/G]GAGTGCAGTTTAAGC | 79658 |
| rs113401081 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147790045 | TTAGCTCAGGCTGCC[A/G]TAACAAAATACCACA | 79658 |
| rs113405927 | snp | C/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889677 | ACTTTGTCTTCTTTA[C/T]AAGTATCTGTTTTTG | 79658 |
| rs113409335 | snp | A/G | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147878800 | TTTTTTTTTTGAGTC[A/G]GAGTCTCGCTCTGTT | 79658 |
| rs113418490 | in-del | -/GGAGAA | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148062920 | CAGATTGGAGAACCT[-/GGAGAA]GGACAGTAAGACAGC | 79658 |
| rs113421946 | snp | A/T | 0.0376037 | 0.131863 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147974432 | TGAAAAGCATCAAAG[A/T]TCATATTAATCAGGG | 79658 |
| rs113424663 | snp | C/T | 0.0596104 | 0.162024 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147902485 | GTAATCCCAGCACTT[C/T]AGGAGGCCGAGGTGG | 79658 |
| rs113436999 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148024015 | TCGTTGCCACGTGGC[C/T]CTGTTGTTTCAGTGT | 79658 |
| rs113444215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148006011 | GATATGGGGGTCTAA[A/G]TATCTCTTTCCCTTA | 79658 |
| rs113446210 | snp | A/C | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147816342 | TCTGTCATGTGCAAT[A/C]TTGGCCTTGAGCTCT | 79658 |
| rs113472688 | snp | G/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148057703 | CCCCATGGTTATTAG[G/T]TGCTTCCTCCACTCT | 79658 |
| rs113475691 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147845780 | TGCCTTAAGTTATCT[A/G]TGAGACACTGTGTGT | 79658 |
| rs113485263 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147994948 | TATTGATGGGTCGAC[A/C/G]TGGAAAGGTCCTCTG | 79658 |
| rs113488570 | snp | A/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147982351 | GGAGTTCCCTGGGTT[A/T]CTTTTCTTTCTTTCT | 79658 |
| rs113493310 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147750602 | TACATATAAAATATC[C/T]TTTTTTTTTTTTGGG | 79658 |
| rs113505893 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148068124 | TGACCACCAGCCAGT[C/T]CTGCTGTGTCTTTCC | 79658 |
| rs113514531 | snp | A/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147908811 | ATACACAAATTTTCA[A/T]TAAGTCCCTTTTAAG | 79658 |
| rs113516826 | snp | A/C | 0.115788 | 0.21092 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147893458 | ATTATTATTCTCTCT[A/C]TATATAATACTATTC | 79658 |
| rs113521328 | in-del | -/GAG | 0.0821764 | 0.185298 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147892188 | TTATGTTGAGGAAGA[-/GAG]GAGGAAATCACCTAT | 79658 |
| rs113526008 | snp | C/G | 0.0429648 | 0.14013 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147886296 | CAGATGATGCTTTCA[C/G]CACTTGGCTTCTTGA | 79658 |
| rs113536803 | snp | C/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147962231 | TGAAACACTGCTCGT[C/T]TCTGCCTTCTTCCTT | 79658 |
| rs113542478 | snp | G/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147949881 | TCTTTTCTTTTGCTG[G/T]GTGGGAGGAATTTGT | 79658 |
| rs113576908 | snp | C/G | 0.0926964 | 0.194308 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147982116 | GAGTATGGGTCACTG[C/G]AGCTTTGACTTCCCA | 79658 |
| rs113578267 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148050397 | TTTTTTTTTTAAGAT[A/G]TAGTCTCGCTCTGTT | 79658 |
| rs113592691 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148033647 | TGTGTTTAGTTTACA[A/C]ATGTTTCAGCTTAAC | 79658 |
| rs113596751 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147925242 | AACACCCTGAAAACC[A/G]AAAGCAGGCATTCTT | 79658 |
| rs113600660 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147882184 | AATAACCTTGGAGGC[C/T]AGGTGCAGTGGCTCA | 79658 |
| rs113611599 | snp | A/G | 0.0121278 | 0.0769207 | synonymous-codon, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147875047 | ATTTGAAGGAACAAG[A/G]TCAGAAGTGGAAGAG | 79658 |
| rs113616336 | snp | C/T | 0.444444 | 0.157135 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147984487 | TTTGACCCACGGTGG[C/T]CTTTGGAGGCTGTGC | 79658 |
| rs113629943 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147781474 | ATACGGGGAGCTACT[C/T]TTACATCTTAAATAC | 79658 |
| rs113667816 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148005762 | TTGAGGTTCTTGTGT[C/T]TTGTCCTTCGATGAC | 79658 |
| rs113674584 | snp | G/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148057077 | AATGATGGCAACTGT[G/T]GGCCAACCTCTGGGG | 79658 |
| rs113675524 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147988760 | TTTCCCCCACACTTC[C/T]GTGTAGGAACTGAGA | 79658 |
| rs113681576 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147931429 | ATATCTGAAAAATCA[C/G]AATAATTTGGATATT | 79658 |
| rs113692596 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147878424 | AAAGGCTAGCTTTCA[A/G]TCATCAGTAAGAGCA | 79658 |
| rs113701023 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147827751 | AAATGACTGTAAAAT[A/G]GAGGTAGAAATAGTC | 79658 |
| rs113709800 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147953641 | TTGTTTGTTTTCTCT[A/C]TTTTATTTCCTAATC | 79658 |
| rs113710863 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147750688 | CTCACTGCAACCTCC[A/G]CCTCCTGGGTTCAAG | 79658 |
| rs113717450 | in-del | -/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148040821 | AAAGATTTGGGGGGG[-/T]GTTATTTGGTGTATG | 79658 |
| rs113725394 | snp | A/C/T | 0.0197763 | 0.0975112 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147991551 | GGAGATAGTCACATG[A/C/T]GCATCCTTTACCTAG | 79658 |
| rs113725779 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147838546 | GATTTCTCTTCCTCC[C/T]CTTCTTCTTCACAGG | 79658 |
| rs113727407 | snp | C/T | 0.0715223 | 0.175059 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147745616 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 79658 |
| rs113728535 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148016703 | TACCTGGAGGTAGTG[C/T]CAGATGCCACAGATT | 79658 |
| rs113731047 | snp | C/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147953070 | ATTTGGTGAAGTACA[C/T]TGATTTTTTTTTTAG | 79658 |
| rs113736871 | snp | C/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147746140 | GACAGAGTCTCACTC[C/T]GTCGCCAGGCTGGAG | 79658 |
| rs113738752 | snp | C/G | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147961153 | TTCAGAGTGGTTGAA[C/G]CCTTTAATGATTACC | 79658 |
| rs113747061 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148025403 | GAATCAGGAAAACTC[G/T]TAAGTTTGGTCATAG | 79658 |
| rs113756073 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147803383 | ATTTTGATACATGCA[C/T]ACAATGTGTAATGAT | 79658 |
| rs113762878 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147891879 | GGAATATCACCCTTC[C/T]CCCGCCCCAACAATT | 79658 |
| rs113766157 | snp | G/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147946175 | TACCCTACTTAGTTG[G/T]CTGTCTCCTGCCTCT | 79658 |
| rs113772784 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148037313 | AGTGGATGTTATGAT[A/G]TACTTCTAAGTCTTG | 79658 |
| rs113773616 | snp | A/C | 0.0475351 | 0.146656 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147821931 | TTGTAGCTGTGCCAA[A/C]CTTATGCAAATTACT | 79658 |
| rs113781094 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147784432 | ATAATTTTTAAATTA[A/C]ATAATATATAAGTTA | 79658 |
| rs113787665 | snp | C/T | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148023911 | AGGTTGACCTGCCTA[C/T]CTGGGCCAGGCTTGT | 79658 |
| rs113793144 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147855442 | AATACATTGGACTTA[A/G]TTGTAAATTAAAAAA | 79658 |
| rs113793192 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147929741 | ATTTCATGAAGAGTG[C/T]GTTTTTCCTTCATTT | 79658 |
| rs113805482 | in-del | -/A | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147764485 | TAGTGACTTTGAGGT[-/A]AAAAAAAAAAAACCT | 79658 |
| rs113812536 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147958649 | TCATTTCACGGTAGA[C/T]ACGAATGCCACAGGA | 79658 |
| rs113817469 | snp | A/G | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148014387 | AAAACTGCACCTGGA[A/G]TGTTTTTAAAGGTTT | 79658 |
| rs113820189 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147920636 | CGTGTTCAACGTTGG[C/T]TACATACAATCCTTG | 79658 |
| rs113834404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147931286 | TGCTAACTATCAGAA[C/T]GAATCTCAATCTAAT | 79658 |
| rs113834856 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147792512 | ATAATGAACACCTAC[A/G]AGCTCATCAGGTTCT | 79658 |
| rs113840488 | snp | C/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147964174 | TGACCCCCCTCCCTA[C/T]GAGCCTCCTCTGCGG | 79658 |
| rs113840747 | snp | A/G | 0.021333 | 0.101051 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147937583 | CCAGTAATATAAATC[A/G]TCCTGTTATACACAC | 79658 |
| rs113857955 | snp | A/G | 0.122411 | 0.214991 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148071893 | CCAGAAGTGGCCCCT[A/G]TTCTCTACTGGCCAC | 79658 |
| rs113858796 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148007913 | CTTCGGAGACACTTC[C/T]GTTTCTCAGTAATTC | 79658 |
| rs113861941 | in-del | -/TT | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147957918 | ACTGCATTGGAAAAG[-/TT]AAAACATTTTTTTCT | 79658 |
| rs113870779 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147790685 | CACATTTGGTGGCCA[A/G]TGTTAAAGTTATATG | 79658 |
| rs113890188 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147849380 | TTACTTTCCACATCT[A/G]TGCTGCCTAAACATT | 79658 |
| rs113890335 | snp | A/T | 0.255782 | 0.249933 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147793005 | TAGCTGGGTGTGGTG[A/T]TGCATGCCTGTAGTC | 79658 |
| rs113895407 | in-del | -/CA | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147783813 | ATTATATTTATATAA[-/CA]CACATTAAATTGTGT | 79658 |
| rs113896125 | snp | A/C | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147818629 | CTGCCCTGCATCTAA[A/C]CCAGGCAGAGATGTT | 79658 |
| rs113916624 | snp | C/T | 0.5 | 0 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147864904 | TGTCTCTCGAGTATG[C/T]GTGTAAGCTGCAGGA | 79658 |
| rs113921846 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147986152 | AGGGACTTAAGTGAC[C/T]GGTTTAACCTCATTA | 79658 |
| rs113939862 | snp | A/G | 0.0626037 | 0.165477 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148013677 | TGGGTGACAGAGCGA[A/G]ACTCCATCTCAAAAA | 79658 |
| rs113939921 | snp | A/G | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147839134 | TCTATCTATCTATCT[A/G]TCTATCTATCTGTCT | 79658 |
| rs113964119 | snp | C/T | 0.021333 | 0.101051 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147860143 | CTCCTCTTGCTTCAA[C/T]TGAAAATAACAGGAG | 79658 |
| rs113965571 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147740393 | CAAAACCCTGAACCA[C/T]AGTAATGAGCTGTCT | 79658 |
| rs113973574 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148054944 | GGGTGGCAGCTGGTC[A/G]AAACATTCCTGTCAG | 79658 |
| rs113977593 | snp | C/G | 0.151668 | 0.229849 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147973816 | ATGCCTGACTTATTT[C/G]ACTTAACATAATTAC | 79658 |
| rs113983538 | snp | C/G | 0.0275645 | 0.114116 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147923265 | TCTTATAGTTTCAGA[C/G]ATTGGAGTGTAATTA | 79658 |
| rs113989301 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147895588 | TACTCAGGAGGCTGA[A/G]GTGGGAAGACAGTTT | 79658 |
| rs113999288 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147748140 | ACTCTTGAGAAGTAC[A/T]GTTATGCTAAGACAA | 79658 |
| rs114023294 | snp | C/G | 0.0232847 | 0.105357 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148053339 | AGCCATGGCTGTCAA[C/G]TGGTCAGTGCCCTTG | 79658 |
| rs114028442 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147732829 | GCTACTCACAATCTC[C/T]TACAAAACCGAGGCA | 79658 |
| rs114033334 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147990788 | GGGACGAGGGAGGTC[A/G]GAGCACGAGGATCAC | 79658 |
| rs114050260 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147978856 | TTTGGCCATTTGTCC[A/G]TCTTCTTTTGAGATG | 79658 |
| rs114060404 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148037881 | GCTATATCCTTTGAT[C/T]TCTGTCAATCTTAAA | 79658 |
| rs114071089 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147890357 | AATTTACCAAAGGGT[G/T]ACTTTGAATTTTTCT | 79658 |
| rs114072974 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147861662 | TGCAGGCAGGTCGAC[G/T]TAATGAGTGTCCAGC | 79658 |
| rs114081956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147857900 | TTCTGAGCATTATTT[C/T]ATAGGAACATAACTT | 79658 |
| rs114084380 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147944111 | GTATGTTAAAACGAG[A/T]TTTAAATAATTGATT | 79658 |
| rs114114904 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147850265 | AAATGAACCAATCAG[C/T]AGGCCGTGGACGGGG | 79658 |
| rs114126248 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147973199 | AGCAGGAGGAAAAGC[C/T]AGAATAGACATGGAG | 79658 |
| rs114151092 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147861419 | CCCCGAAGGGCCGCA[A/G]CTCTTCTCTCCTTCT | 79658 |
| rs114168810 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147852419 | AGGATGAAGTTGAAT[C/T]CTCATCTCTTTAGAG | 79658 |
| rs114170339 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147816391 | TTTCTTTTGGGGCCT[A/G]TGCACCTTTGTGGGC | 79658 |
| rs114216089 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147796830 | GCGCCCGGCCTGTTC[C/T]TTATTTCTGGAATGC | 79658 |
| rs114221034 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147805879 | CAGTGTGGATAACAC[A/G]CCTATGAAACTTTAT | 79658 |
| rs114221260 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147770109 | CGTCCTTGCCACCAC[C/T]GACTTAGACCAGGTG | 79658 |
| rs114226998 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147914181 | GCTTTATTGAGGTAT[A/C]ATTTGCAGTCAGTAC | 79658 |
| rs114232707 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147741051 | TATATTTGTGAGATT[C/T]ATCCAATTGGATGTA | 79658 |
| rs114239565 | snp | A/C | 0.02016 | 0.0983543 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147909366 | ACTCAATTGCCAGCT[A/C]ACTGCTGAAGAGATT | 79658 |
| rs114254585 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147847872 | TATTTAGCAACTTAT[C/T]TAAAATGTGCAATCT | 79658 |
| rs114294973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147871394 | AGGACTATTCGTGTC[C/T]GTCTCTCTATTTTAC | 79658 |
| rs114305661 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147776166 | GTGTAGACCTGCTAG[A/T]GGCAACAGATACAAC | 79658 |
| rs114308662 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147751365 | GAGTAGATAATAGTT[A/G]TTGTTTTTTTTTTTT | 79658 |
| rs114331812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148028212 | AGTAGCGTGACTGAG[A/G]CATGGCAGGAGCAGA | 79658 |
| rs114344261 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147773545 | GTACACTTAAATATT[C/G]TATTCTGAGTTATAA | 79658 |
| rs114389766 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147970642 | CATGTAATTAAAGCA[A/G]GATTGCTCTAGATGA | 79658 |
| rs114402366 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148054044 | ACAATTAAGTCTTGC[A/G]TCAGTCATTTTTGGT | 79658 |
| rs114410404 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148058328 | CTCGTATTGTATAAC[C/T]GTAGTGAAATATCTT | 79658 |
| rs114411511 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147990054 | CCCTGACTTCCCGCA[A/G]CACTCCTGATATTCA | 79658 |
| rs114413384 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147953065 | TTTTCATTTGGTGAA[A/G]TACATTGATTTTTTT | 79658 |
| rs114416092 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147824352 | CGGATTCTTTTTTCT[A/G]TATTCTTGAAAATGA | 79658 |
| rs114419241 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147910198 | ATTTTTAATTTTTTT[G/T]TTGTTGTTGAGATGG | 79658 |
| rs114432467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147746759 | GAGGGTGTACCTTTC[A/G]CCTGTTTCATGACAG | 79658 |
| rs114442693 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147993921 | CTAGTTCATGCAAAC[C/T]GTGAATCAACAGCCA | 79658 |
| rs114444763 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147840907 | AAATACAAGATAAGC[A/G]TAAGAGCATTGTTTT | 79658 |
| rs114447064 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148024639 | TGGATAGTTAATTTC[C/T]AGAGGAAGGGCATGA | 79658 |
| rs114453038 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147972652 | GTTGTCTAGGGCCTT[A/G]TCAAGGATGCCAGAT | 79658 |
| rs114460849 | snp | A/G/T | 0.0368353 | 0.130617 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147868263 | TTTTTTTGAGACAGG[A/G/T]TGTCACTCTGTCGCT | 79658 |
| rs114465106 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147903817 | ACCGAATAATACTCC[A/C]TTGTCAGGATGTACT | 79658 |
| rs114466769 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147760980 | AAGAGCTGGTTGTAG[C/G]TAAAAAGAGGCAGTT | 79658 |
| rs114468532 | snp | A/G | 0.0126979 | 0.078662 | upstream-variant-2KB | ARHGAP10 | GRCh38.p7 | 4:147731463 | ATTTAGTGCGGATAC[A/G]CAGAGAAGTGTAATA | 79658 |
| rs114469589 | snp | C/T | 0.021333 | 0.101051 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147788025 | CGTGAGAATTTACTT[C/T]AGGATTTATCATCGG | 79658 |
| rs114470728 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147829955 | TGCCAGGAGAGAGAA[A/G]GTGGAGCTTGCCTGA | 79658 |
| rs114532241 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911481 | CGTTTTCCTGTCTCA[A/G]CCTCCCGAGTAACTG | 79658 |
| rs114546049 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147807901 | TTCATGAAGGTCCTC[A/G]TCCTCCTTTGGTTGT | 79658 |
| rs114547541 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147850228 | TCAGCACTCTGTAAA[A/G]TGGATTAATCAGCGC | 79658 |
| rs114559815 | snp | C/G | 0.0748431 | 0.178382 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148068860 | TGAGTTGGTGGAAGG[C/G]ACCTGCCTCTCTTTG | 79658 |
| rs114565316 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148056725 | AAATCCAGGATGCCA[C/T]GTTTCTATAAGCAAC | 79658 |
| rs114569961 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147752868 | CCTTTGATTAAATTT[A/G]CTGCTTATCTCATGC | 79658 |
| rs114586724 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147976730 | GAAGCTTCTGCTGTC[A/G]TGTGGCTCTGTAAAT | 79658 |
| rs114599615 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147969082 | AATAATGAATTCAAT[A/T]CATTTTGAGGGGGTT | 79658 |
| rs114620525 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148007821 | TTTGGAACTTAAAAA[C/T]TGATACTGTGGCTTG | 79658 |
| rs114624783 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148033904 | ATGGTTACGTTGTCC[C/T]GGCGTTTTGGGGATC | 79658 |
| rs114628841 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147781003 | AGGGCTCAGATTTGC[A/C]TTTGATGGTGGGAAA | 79658 |
| rs114646078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147895857 | AAGTGTTCATTATTT[A/G]AAGTGTAATATTAGC | 79658 |
| rs114648412 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147877886 | TTCTCTTGGTTCTTA[A/C]GATTTTTTTAGACCT | 79658 |
| rs114649881 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147898183 | TCCTTAGGCTGCCTT[A/T]GGCTGCATTTCTTGT | 79658 |
| rs114650109 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147987220 | GCTTTCAGCAAAATC[A/T]TTGTAATTAAGAATG | 79658 |
| rs114654188 | snp | C/T | 0.0584853 | 0.160693 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147916014 | CTCAGGAGGCTGAGG[C/T]GGGAGGATCACTGGA | 79658 |
| rs114684358 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148045403 | TCTGGGGAGCTAGCT[A/T]AATCAGAGCCTGGAA | 79658 |
| rs114694877 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147789526 | TGAACTCCTGGCCTC[A/G]GCCTCCCAAAGTGCT | 79658 |
| rs114717516 | snp | C/T | 0.0836354 | 0.186609 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147779185 | GGTTCAGGGGCTGCA[C/T]GTGAGAACCACTGCT | 79658 |
| rs114768513 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147832361 | TTTTTTTTTTTAAAA[A/C]GAGGAGTCCAGGCAC | 79658 |
| rs114769969 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148038142 | CAACCCAGACTTTAT[C/T]TTAGCAGAGTAGAAA | 79658 |
| rs114771338 | snp | A/T | 0.0275645 | 0.114116 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147755034 | TTGCAGTGAACCGAG[A/T]CTGCGCAGTTGCACT | 79658 |
| rs114771985 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147796820 | GTGAGCCACTGCGCC[C/T]GGCCTGTTCCTTATT | 79658 |
| rs114781280 | snp | A/G | 0.021333 | 0.101051 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147787101 | CTCTTCTCACTAGTC[A/G]TATCTCCTCAGCAGA | 79658 |
| rs114786206 | snp | A/G | 0.0038404 | 0.0436515 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147955394 | GTATTATGTAAAGGT[A/G]TATAGGAACAGTTTT | 79658 |
| rs114787578 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147954278 | ACTTGTTCTGTTACT[A/G]AAACAGAGAGGTGTT | 79658 |
| rs114796502 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147976247 | CTCTTTAAAAAACAT[A/C]TAGCCAAAAATGCTT | 79658 |
| rs114803294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147871985 | GCACATGTGAGTAGT[C/T]CCTGTACTCGGGAGG | 79658 |
| rs114806022 | snp | G/T | 0.0704125 | 0.17392 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147785592 | GCTTTCAAACAGAAG[G/T]CATCCAGACAACCTT | 79658 |
| rs114821318 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147994509 | ATTAATAGGTTATGG[A/G]GAAGATTTATAATCC | 79658 |
| rs114821470 | snp | C/T | 0.079617 | 0.182947 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147925320 | GGCAGAGGGCAGCAG[C/T]GAGACACAACATTAG | 79658 |
| rs114849938 | snp | A/C | 0.126564 | 0.217402 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147887450 | TTCATCTTAAAAAAA[A/C]AAAAGCCACTACAGC | 79658 |
| rs114864244 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147771453 | TGAGGCATTTTTGTT[A/G]TTGTTCTTGCAAACA | 79658 |
| rs114870609 | snp | A/C | 0.0174175 | 0.0916809 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147876823 | GTATACAACTTGTCT[A/C]ATTTATCCATAAAAC | 79658 |
| rs114894739 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147885776 | ATGTTGCCATTTCCT[A/G]TAGTTGTTTTTCTGT | 79658 |
| rs114911667 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147963055 | TCCTTTAAGAAAAAT[A/G]TCAGGCATACCTTCC | 79658 |
| rs114939969 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147924434 | ACAGAATAGAAATGA[A/G]GAAAATTAATAGGAC | 79658 |
| rs114990426 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147968729 | AACATTCCTGACTTC[C/T]GCCTCTAAGATGGGG | 79658 |
| rs114994569 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147888334 | AGCTGCCTACTCAGT[A/G]TTGCTTCTGGGGTGT | 79658 |
| rs114995420 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147844696 | TTCGGTCAATCTCTC[A/G]TTACTTTGACACCAC | 79658 |
| rs115003253 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148059746 | AGCTACCAAATTAGC[C/T]TACCATCGTTTCCGG | 79658 |
| rs115027050 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147963844 | CCTTCATTCCAGCCT[C/T]TGCTGTGACAGGACA | 79658 |
| rs115032551 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147930382 | ATTTATTTTTCAATT[C/T]ATTTGTTAAATATAT | 79658 |
| rs115035727 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148005505 | TCAATTATTATGGCC[C/T]TTTTGTGGTTTTCTT | 79658 |
| rs115037773 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147972487 | AAAGTGAAGTGCTTG[C/G]GTTTGAACTGAGATT | 79658 |
| rs115042798 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147778152 | AGAGGAGCAAAATGA[G/T]TTGAAATAGATGGCA | 79658 |
| rs115045594 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911424 | CTGCAGTGCAGGGGC[A/G]CAATTTCAGCTCCCT | 79658 |
| rs115053194 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147836455 | GATAATTGAACTAGT[C/T]GATTTGGGATATATA | 79658 |
| rs115063039 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147743307 | AAGTGCTGAGATTAC[A/G]GGTGTAAGCCACCGC | 79658 |
| rs115080609 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147822514 | ATTTTTTCAGCATCT[C/G]TTCTGTGGCAGGGTA | 79658 |
| rs115125587 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147968868 | ATGAATATTCCAGCT[C/G]CTGTGGGAAAGCAGG | 79658 |
| rs115129971 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148059716 | TGAAGGGTCTGAAAC[C/T]GTACCCTGCTTGCGA | 79658 |
| rs115140690 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147974133 | ATTCTCCATAGGGGT[A/C]CATTCCCACCAAGAG | 79658 |
| rs115148499 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148055151 | AGAGATGTAATTCTG[C/T]GCCTGTTCTCTTACA | 79658 |
| rs115152490 | snp | C/T | 0.00229253 | 0.0337789 | synonymous-codon, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148023388 | GCCCGTGGCCGTCTA[C/T]AATCTTTGTCTGGAG | 79658 |
| rs115160295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148066592 | CATTTGTACATATGT[A/G]CACACATGTGCACAC | 79658 |
| rs115178935 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147884828 | GCTTGAGATGGGGCA[A/G]CGGCCTGAACTTGAA | 79658 |
| rs115198059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147935037 | CTGATGAATAAATAT[A/G]TGACAGTTGAATAAA | 79658 |
| rs115202263 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147762197 | ATTTTTAGTAGAGAT[C/T]TGGTTTCACCATGTT | 79658 |
| rs115210835 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147988813 | TCACCTCAGACTCAT[A/G]CTTTATTCTGTCAGT | 79658 |
| rs115214541 | snp | A/G | 0.0185938 | 0.0946107 | upstream-variant-2KB | ARHGAP10 | GRCh38.p7 | 4:147731161 | GGCGTGAGCCACCAC[A/G]TCCGGCCTAAGGTAT | 79658 |
| rs115231537 | snp | C/G | 0.0189856 | 0.0955633 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147848642 | AAACAACATCCATTT[C/G]TTATTTTTCTCATTT | 79658 |
| rs115258579 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147955158 | AGTTAATAAAGTGAT[C/T]CGTTTATGTATCTTT | 79658 |
| rs115281340 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147859352 | ATCTTGGCTCACTGC[A/C]ACCTCCACCTGCCGG | 79658 |
| rs115282357 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147888530 | TTTTTTCTTAAAAGT[C/T]ATACATGCTTATTTT | 79658 |
| rs115286159 | snp | A/G | 0.0825414 | 0.185628 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147814817 | GGGCCCATTCTTAAT[A/G]ACCTCATTTTAACTG | 79658 |
| rs115294075 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148032096 | TTTTCTCCTCCCACT[C/T]CTCTCCCCTTCTTTC | 79658 |
| rs115297352 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147901061 | ATGTCCTTTGTTTCA[A/G]AAACTACAGAATTTT | 79658 |
| rs115298858 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147885964 | ACTGGCATAATGCCA[C/G]AAGTGGAGAATTCCA | 79658 |
| rs115312866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148022016 | CTTTTTGACTGTGCA[A/G]TTAAAACTCCAGCAT | 79658 |
| rs115325027 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147914567 | GCGCTCCCCCCCCCC[C/T]CTTTTTTTTTTTAAC | 79658 |
| rs115333318 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147860737 | AAGCAGATTTCCTAA[A/C]TAACTTTATGTGAGA | 79658 |
| rs115344336 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147751688 | TGCTTTTTTTGGAGC[A/G]CTTGTGTTTCAGAGA | 79658 |
| rs115346185 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889925 | TTTTTTTCTCTTGTT[C/T]GGGAAGCCCAGAGGT | 79658 |
| rs115386858 | snp | A/G | 0.0209421 | 0.100162 | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147782032 | TTTACCGCTTAGTAT[A/G]TCTCTTGTGACCTTG | 79658 |
| rs115399905 | snp | A/G | 0.00478085 | 0.0486577 | upstream-variant-2KB | ARHGAP10 | GRCh38.p7 | 4:147730157 | TGATTCTACTTTTTG[A/G]CTATTACGAATAATG | 79658 |
| rs115400892 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147773243 | TTCATTAATGTACAT[A/G]TGTATGTATATATTA | 79658 |
| rs115444864 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147996008 | AGGCATCAGCCACTG[C/T]GCCTGGTGGTCCATC | 79658 |
| rs115452441 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147868697 | TGGGAGAAGGTAGGG[A/G]ATGGTTTCGTGATGA | 79658 |
| rs115497478 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147901365 | TGATCCCTTTAATGT[A/T]AAAGTAATGCGTTGC | 79658 |
| rs115527976 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148020763 | CAAACATACTCGTGC[A/G]TGTATCTTTATAACA | 79658 |
| rs115529877 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148007888 | AGCTTTGAATGTTCC[C/T]GGTCACAGTCTTCGG | 79658 |
| rs115533936 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147903679 | AGTTTGACCTTTTCC[A/G]GAGTGTCATCTACTT | 79658 |
| rs115536182 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147828807 | TAAGAAAAAAAGTCA[A/G]TGTTTCCCTCCACAC | 79658 |
| rs115554026 | snp | C/T | 0.0654984 | 0.168698 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147945724 | TCATGGTGCCACCCT[C/T]GGTTTTCTGTGTCAT | 79658 |
| rs115559928 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147955618 | ATGTAAAGCCAAGAC[A/G]GGATTCTTGTCCCAT | 79658 |
| rs115561721 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147862360 | GCAGTGGGCCTTCGC[C/T]GGCCCCCAAGAGCAC | 79658 |
| rs115563034 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147888224 | TTTATGACCTTGTCC[A/G]GTCTTACGACTTTAT | 79658 |
| rs115571120 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147767830 | ATAATTGTGATGGCA[A/G]TGGAGGACCAGTGAA | 79658 |
| rs115573675 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147818863 | TTATAATTATTAAAA[G/T]AAATAGAATATGGTG | 79658 |
| rs115574047 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147793743 | CTCCTCTGCTGAGGC[A/G]CCTTGCAGAAACAAA | 79658 |
| rs115576182 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147932654 | GGACCTGTCAGAAGG[C/T]GGGGGTGGGAGGAGG | 79658 |
| rs115582546 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147787365 | TTCAGTTTAGGAAAC[A/T]CATGAACACAACATC | 79658 |
| rs115590242 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911168 | TTCCATTTTATAAAG[C/T]TTTGTGAATAGTGAA | 79658 |
| rs115613443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147885769 | CCTTTAAATGTTGCC[A/G]TTTCCTATAGTTGTT | 79658 |
| rs115620709 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148032221 | CCCATTGACTCAGTG[C/T]CTGCGTCTGCAAGCC | 79658 |
| rs115654716 | snp | A/G | 0.0711525 | 0.174681 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147990869 | AAATACAGAAAAACG[A/G]GCCTGGTGTTGTGGT | 79658 |
| rs115665622 | snp | G/T | 0.0205511 | 0.0992634 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147996747 | GTAACTGTATTTGAA[G/T]GCAGGGTCTTGAAGG | 79658 |
| rs115666524 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147978116 | TGTGAATAATGCTGC[A/G]ATTAACATACAAGTA | 79658 |
| rs115712360 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148062009 | AGATTAGAGCAGGGC[G/T]GGGAGCTTGAGAGGA | 79658 |
| rs115713504 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148033251 | TGGATGTACTTATAA[A/G]AGGACCTTGTATTCT | 79658 |
| rs115720924 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147990859 | GTCTCTACAAAAATA[C/T]AGAAAAACGGGCCTG | 79658 |
| rs115722551 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147988353 | CTAATTTCATTTACT[A/G]GATCATGTTTTCTGA | 79658 |
| rs115728728 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147955740 | AAGTATTTAATTTGC[A/G]AAAGGTTGTGGAGAT | 79658 |
| rs115736594 | snp | C/T | 0.030278 | 0.119257 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148069125 | CTAGGAGAGGAGCCC[C/T]AGATGGGTATTTTGG | 79658 |
| rs115749446 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147984203 | AGTAATAGCTGCCTG[A/G]GGAATGGGCAGAGGG | 79658 |
| rs115750886 | snp | A/G | 0.030278 | 0.119257 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147977593 | TTAGTATAATATGGC[A/G]TAGTAGGCTCTAAAG | 79658 |
| rs115753644 | snp | A/G | 0.00143386 | 0.0267371 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147913094 | CAGTTGGATAAGATG[A/G]GGTTCACAATTATCA | 79658 |
| rs115763500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148067960 | TGCCTAGCTGTTTCT[C/T]TGGGGCTATGCCTCC | 79658 |
| rs115772146 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147888433 | CTTGGGAGTGGGAGT[A/G]GGGGTAGTTACATTC | 79658 |
| rs115772638 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147862057 | CATGTCATCCATGGC[A/G]CCCAAGGTATTTGTG | 79658 |
| rs115776553 | snp | A/G/T | 0.00289895 | 0.0379619 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147881956 | TTGGAATTATTGGAC[A/G/T]TGGTGAAAGAGTCGT | 79658 |
| rs115779097 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147850529 | CCACCTTTAAGAGCT[A/G]TAACAGTCACTGCAA | 79658 |
| rs115779628 | snp | A/C/T | 0.00994216 | 0.0698866 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147817388 | GAGTGTCTGTTTGTC[A/C/T]AATATCTCATGGTCT | 79658 |
| rs115788917 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147750458 | GTGCATAATCTAATC[A/G]TAGTTTACATATAAC | 79658 |
| rs115810467 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147952419 | ATTCTTGCCAACTCT[C/T]AAGCTGGTCAATCTT | 79658 |
| rs115817780 | snp | A/C | 0.0352966 | 0.128072 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147733537 | AGTTCAGTAATTCTC[A/C]GCCTTAGGTATTCGT | 79658 |
| rs115821968 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147742466 | TTACAGGAGAAATAG[C/T]CTGTGAACACTTTTT | 79658 |
| rs115836638 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147832926 | GGACAACTGTAGCTC[C/G]TCAGTATTTCAGTCC | 79658 |
| rs115859558 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147918773 | GAAAAGAAAGAATAT[C/G]TCATGTCTCTCACAT | 79658 |
| rs115874250 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147990149 | TCCTTCAGGTCAGGT[A/C]TTCATGGTGCAACCT | 79658 |
| rs115877889 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147945888 | GCAAAGAGAGGGGGT[C/T]CCACCAGCGGGCTCC | 79658 |
| rs115886598 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148049636 | AGAGATTCCTTGTCC[A/G]TATTTCTGCTGATAC | 79658 |
| rs115893921 | snp | G/T | 0.0178098 | 0.0926698 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147876656 | TGAGAATGTTAGAAT[G/T]ATTTGTATTATATGC | 79658 |
| rs115902957 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147770750 | AGTTACTTAGCCCAT[C/G]TGAGCTTCGGTGTTT | 79658 |
| rs115914598 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148029109 | ATAAATAGTGTATAT[A/G]GAAATAGTGTATATG | 79658 |
| rs115915583 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147986039 | AATTAAAGCTCACAG[A/G]GTTTATCTTTATGCA | 79658 |
| rs115929285 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147777708 | CCAGCAGCATCTTTA[G/T]TATACCTCTGGAGGG | 79658 |
| rs115939577 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147981705 | TATTCTCTTAGGTCT[A/G]GAAGTAATTGTTTTA | 79658 |
| rs115988078 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148015442 | AGGGATAACTAGGAT[A/G]CTTTCCAGCTCCAAG | 79658 |
| rs115992530 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148068709 | GGGAGATAGGACAGA[G/T]CCCAGGACGCAGCCT | 79658 |
| rs115994430 | snp | C/T | 0.030665 | 0.119967 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148032895 | GACGGCTGTGGAAGA[C/T]TCAGCAAGTCAAGTC | 79658 |
| rs115994729 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147855142 | AGCAGTCTTGTGGGC[A/G]AATGCAGGGGCCTGA | 79658 |
| rs115995981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147884916 | TTGTATTTCTCAAAG[C/T]TCATTCTGGCAGAGT | 79658 |
| rs116004061 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147837643 | GAATCTCTGGTCACT[G/T]TTTTTTTTTTTTTTT | 79658 |
| rs116018286 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147971954 | GAATAGGCAAAACCC[A/G]GGGACTGGGTTTGTA | 79658 |
| rs116036892 | snp | A/C | 0.0168055 | 0.0901129 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147915998 | CTTGTAGTGACAGCT[A/C]CTCAGGAGGCTGAGG | 79658 |
| rs116045846 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148007902 | CCGGTCACAGTCTTC[A/G]GAGACACTTCCGTTT | 79658 |
| rs116055439 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147809873 | TGATCTGGGACCCAG[A/G]GCTTGGGGACCCCTG | 79658 |
| rs116057864 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147910434 | TTTCAAGTATGCAAC[C/T]TTCAACTTCTTGTCT | 79658 |
| rs116092804 | snp | C/G | 0.126219 | 0.217206 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147820322 | AGACAGTCTCATTCT[C/G]TAACCCAGGCTGGAG | 79658 |
| rs116101255 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147775246 | TCAGCATTCTCACTC[C/T]TGGAGTCCAGGCCTA | 79658 |
| rs116112254 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147781464 | ACATTTAAAAATACG[A/G]GGAGCTACTTTTACA | 79658 |
| rs116143842 | snp | A/G/T | 0.00115257 | 0.0239792 | missense, intron-variant, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148063227 | TCCAACTCAGCTGTG[A/G/T]CACCTCTTTCACCCG | 79658 |
| rs116166388 | snp | G/T | 0.0448719 | 0.142907 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911420 | CAGGCTGCAGTGCAG[G/T]GGCGCAATTTCAGCT | 79658 |
| rs116173004 | snp | C/T | 0.0637235 | 0.166737 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147979893 | CTTTGCATCCTGTAT[C/T]CTGAAACTCTGCTGA | 79658 |
| rs116178140 | snp | A/C | 0.0236746 | 0.106192 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148027049 | GGAAAGTTCAGGAGG[A/C]TATATGAGATCAAAG | 79658 |
| rs116179783 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147895626 | GGAGGTTCAAAGCTG[C/T]AGTGAGCCATAATCG | 79658 |
| rs116188652 | snp | A/C/T | 0.0154597 | 0.0866004 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147769563 | GTATGTTAACAAGTT[A/C/T]TTTCTACAGAGATGA | 79658 |
| rs116229698 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147931154 | CAGTGTTGTGGGAGA[G/T]TGGAGGAGACAGATG | 79658 |
| rs116241360 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147995488 | CTTGCCACATGTTAC[C/T]GTATATTATGTTTTC | 79658 |
| rs116252974 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147876907 | GAGGCACTGAGAGGT[A/G]AATAATGTTCCCTAG | 79658 |
| rs116267654 | snp | C/T | 0.0648419 | 0.167978 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147973437 | TGTATTTATGGGGTA[C/T]ATGAGATATTTTGAT | 79658 |
| rs116272057 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147777784 | GGGGAGTGGACTCTG[C/G]TTTTCATTTCTTTGA | 79658 |
| rs116292728 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147958827 | TGTCTTCGATAAGCT[C/G]CATGATCACATCTTT | 79658 |
| rs116301986 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147986194 | ATCTATGAAATAAGA[A/C]AAACGGAACTACCTC | 79658 |
| rs116305294 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148040871 | TCTCCTTAATATTCC[A/G]TCTTGGCTGAACATT | 79658 |
| rs116323177 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147888216 | CACACTTTTTTATGA[C/G]CTTGTCCAGTCTTAC | 79658 |
| rs116330399 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147968182 | TATGGGGGAACATAA[A/G]GAAAAAATGGTTTTA | 79658 |
| rs116331883 | snp | A/G | 0.029116 | 0.117091 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147795608 | CGTGGTGCTTGGTAC[A/G]TAGTAGGTGCTCAGT | 79658 |
| rs116342460 | snp | A/G | 0.021333 | 0.101051 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147819802 | GACCTTAGGTGATCC[A/G]CCCGTCTCGGCCTCC | 79658 |
| rs116356092 | snp | A/C | 0.0228947 | 0.104514 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147863239 | CTCTGTACCTATTAA[A/C]AATAACTCTCCATTC | 79658 |
| rs116372707 | snp | A/T | 0.0633504 | 0.166319 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147988512 | GCTCTGAAGCTTTAG[A/T]ACATTAAGACCCACT | 79658 |
| rs116376857 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148005467 | ATAGTGAATTTTACA[A/G]TATTCTGTATGTATC | 79658 |
| rs116392022 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147949232 | AGGGATGTATACTTA[C/T]ATCAGTATTGCCACT | 79658 |
| rs116397122 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148070831 | GCTGCCACGCCTGCA[C/T]CTGACCATGGTTGGG | 79658 |
| rs116410624 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147811758 | GCTTGCAGATTGGTC[G/T]CTAGCCACTTGCAGA | 79658 |
| rs116421587 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147964620 | TCCTGTTCAACCTGT[A/C]ACATGCAATAGCCTA | 79658 |
| rs116429035 | snp | C/G | 0.0352966 | 0.128072 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147759154 | GCTGATAGTAATAAA[C/G]TATTGTAATAAAATA | 79658 |
| rs116458648 | snp | A/C | 0.0509478 | 0.151255 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147768576 | GAAGCCAGAGACTTG[A/C]ACATAATGAAATAAT | 79658 |
| rs116470089 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148049448 | TCTTCTAGGGTCGTG[C/T]GTTGCTGTCCTCCCA | 79658 |
| rs116479357 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147871845 | GTGGCTCACGCCTAT[A/G]ATCCCAGCACTTTGG | 79658 |
| rs116483167 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147838402 | TTCAGCCCATGATTT[C/T]GAGGCTGTAGTGATC | 79658 |
| rs116493319 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147937442 | AGTACTGAGGATTAG[C/G]ACGTCAACAGATGAA | 79658 |
| rs116510653 | snp | C/T | 0.168135 | 0.236216 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147758933 | GCGGTGAGCAGAGAT[C/T]GTGCCACTGCACTCC | 79658 |
| rs116530656 | snp | A/T | 0.040671 | 0.13668 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147736925 | GCGAAGAAGGATGGT[A/T]TTCTACTTTTCTGTA | 79658 |
| rs116540575 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147793238 | TATGTGTGTGTGTAT[A/G]TATATGTATGGTAGG | 79658 |
| rs116541949 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147779984 | CTTTTGCTCTTCGTA[C/T]ATAAGCCTTGTTACA | 79658 |
| rs116542854 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147932204 | AAGGAACACACTATC[C/G]GTGGGAGTGTGAATT | 79658 |
| rs116548741 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147971879 | GTTATTTGGCATAGT[C/T]GAAGGGCATGGGAGT | 79658 |
| rs116563052 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147910303 | GCTGAGATTACAGGC[A/G]TGAGTCACCTTGCCT | 79658 |
| rs116573959 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147933590 | AAGCCCAGGCTTGCC[A/G]CGAGTCTCTTCAGGA | 79658 |
| rs116577751 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147898602 | TTATTTTTTGGGATT[C/T]GAATTACCTTATGTC | 79658 |
| rs116603722 | snp | A/G | 0.0737376 | 0.17729 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147863740 | TGAAGCCACAAAAAT[A/G]TGATTTTGAGGAGTG | 79658 |
| rs116623946 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148070078 | ATCATGTGTCTGACA[C/T]GGTGCTAGGTGCTGG | 79658 |
| rs116643026 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148010110 | ATTCCCCTCCACTTT[A/T]TTTTTGTCATGAGGT | 79658 |
| rs116648976 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147874696 | AACTTATGTTTTAAA[C/T]CTAAAATTTAGTAAT | 79658 |
| rs116649031 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147996283 | AACAGAAAGGCAGTC[A/G]AAAACAAAACATCAA | 79658 |
| rs116665950 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147839792 | GACTGTGGAGGATAG[A/T]TTAAGATAACATAAC | 79658 |
| rs116705132 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147988991 | TTGGATGCTCCTTAT[C/T]GGGGACCTGCCCCGA | 79658 |
| rs116715216 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148027287 | AGCTTATTTAGGCAA[C/T]TTAAAAAAATATGAC | 79658 |
| rs116721339 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147979653 | TAATGATACTGATTC[C/T]TCCAACCCATGAGCA | 79658 |
| rs116751768 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147738637 | AAGCATTTAGTATAA[A/G]TGCTCAAAGGTTAAC | 79658 |
| rs116752517 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147777942 | CATGCTAGAAAGGCA[C/T]GTTGCAGGTCCAGCC | 79658 |
| rs116765933 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147896201 | TCCTTCTCTGGTTTT[A/G]GTACCAAGGTTAAGA | 79658 |
| rs116789287 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148042274 | AATGACTGTCATAAC[C/T]GAATATCTTTTGAAG | 79658 |
| rs116875185 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147879960 | AAAGAAGAGTGATCT[A/G]CGATAAATTTTACTG | 79658 |
| rs116900037 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147802638 | GGTGGCCAGCTCTGC[C/T]TCGCAGGAAACCAGC | 79658 |
| rs116922450 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148035550 | ACATTATTTGGCTTC[A/T]TTATAGTTCCCATTT | 79658 |
| rs116924029 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147991508 | GAAAGCCCAGGTATT[A/G]GAGACTAAGTGCCCA | 79658 |
| rs116994988 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147817183 | GGATTATAGAACATG[C/T]TGCATTTCTAAAAGC | 79658 |
| rs117039484 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148057412 | TCTGAGATCTGTGCT[C/G]TCTTGTCAAAACAGG | 79658 |
| rs117052579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147788640 | CTTTTTACACATTTG[C/T]GGTATTTGGTGTGTA | 79658 |
| rs117056209 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147862505 | GCGGGCACCATGGAG[C/T]GCGCAGCCCTGGCTG | 79658 |
| rs117077585 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147961296 | TGTTTCACCGATATA[A/G]GTTTATTCTGTTTTC | 79658 |
| rs117080031 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148043215 | GTTAAATCTGAGGAT[A/G]CTGCAAGGAAGTCAT | 79658 |
| rs117201856 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147837650 | TGGTCACTGTTTTTT[G/T]TTTTTTTTTTTTAAA | 79658 |
| rs117207188 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147870360 | GCCACCGCGCCCGGC[C/T]GCATATATGTATTTT | 79658 |
| rs117210957 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147821778 | GACACACAGGAAGAC[A/G]GCAGCTGTGTGAAGT | 79658 |
| rs117274429 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147872929 | CCTAAGGCTGTCTGC[C/T]GAGAAGACTTAGAAG | 79658 |
| rs117298690 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147785912 | ATTTTCATAATTTGT[C/T]ACCAAATACATTTTT | 79658 |
| rs117299531 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148062186 | GTTGCTGAGTGTCAC[C/T]GTGTTGGAGGATTGC | 79658 |
| rs117343287 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147813762 | ACATGTTTTCCTGGT[C/G]TCTTCGTAATTGTAT | 79658 |
| rs117394610 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147862860 | AGTCAACAAAATTAC[A/G]GTGTTTTTGCTGGGA | 79658 |
| rs117458526 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147982302 | GAAAGTCTGATGACT[A/G]TGTGCCTTGGACTCG | 79658 |
| rs117523998 | snp | C/T | 0.00196225 | 0.0312614 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147965054 | AATCTCGTGTTAATG[C/T]GATCCATTTCTTGGT | 79658 |
| rs117543034 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147793771 | AAATCATCCGTGCCT[A/G]TGTACGTGCCTTCCC | 79658 |
| rs117549994 | snp | A/T | 0.0486741 | 0.148216 | intron-variant, downstream-variant-500B | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147782687 | AGATGCCCAGTACTG[A/T]CTGTGGTACAACTTG | 79658 |
| rs117577516 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147862438 | TGGGAGCATGGGGCT[C/T]CTGCCCTGATAACTC | 79658 |
| rs117613163 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148035851 | GATTTTCTGATCAAA[G/T]AATCTGGACTTTTTT | 79658 |
| rs117666521 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147986702 | ATATAGAATAAGAGT[A/G]TGTCTCACATTTACT | 79658 |
| rs117695957 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147855013 | CGTCACCCCTTCCTC[A/G]GCCCCTTTCTGTGAT | 79658 |
| rs117699172 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147774109 | AGTTGTGATAATGAA[A/G]TGAGTTAATAAATGT | 79658 |
| rs117754734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147987404 | TTTCTAGACTCTGAA[C/T]GCATAGCCACTTCCT | 79658 |
| rs117842405 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147969734 | TTACAGGAATTTTCC[A/G]GTAGCGTCGGCAAGC | 79658 |
| rs117898721 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148015453 | GGATACTTTCCAGCT[C/G]CAAGATTCTGAGTTT | 79658 |
| rs117923162 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147913857 | GTGTGGGTCCCTGTT[A/T]AAAAAAATCAGCTTG | 79658 |
| rs117982639 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147747754 | CATTTATTTCAGCTG[A/T]CAGTGAGAGGAATCA | 79658 |
| rs118018087 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148004932 | TTTTGTTTTCAGCTG[C/T]TGAGATTATGCTAAT | 79658 |
| rs118036121 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148047348 | CTGTCCCACCCAAGA[A/T]GTTTCCCCACTAGTT | 79658 |
| rs118046330 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147900045 | CTCTCTGCTTTTTTC[A/G]TTGTGTATTTTCTGA | 79658 |
| rs118050800 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147990427 | TTCTGCTAGACTTCA[A/G]TTAATCTTCCAATTT | 79658 |
| rs118057129 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147807072 | TAATTCTGCTGAACA[A/G]TTTGAGAATGAAACT | 79658 |
| rs118091874 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147854247 | ACAATTAAGAAAAAA[A/T]GTGTTGCCACCATAA | 79658 |
| rs118158362 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147886217 | CATTTTGGATAAAGG[A/G]TACTCAACCGGTGCA | 79658 |
| rs118175577 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147979338 | TGTTTTTTGTCAGCT[C/G]TGTCAAAGGTGACTT | 79658 |
| rs137866409 | snp | A/G | 0.0637235 | 0.166737 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147830767 | TCACGTGATCTGTGC[A/G]AATTGGTCTGCCAAA | 79658 |
| rs137869195 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147757088 | CTTCTTTAAATTTAC[G/T]GAAAAATATAAATCA | 79658 |
| rs137887892 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148067305 | TGTGTGTGTGTTTGC[A/G]CCTTACATCTTCTGT | 79658 |
| rs137889765 | in-del | -/TCTTT | 0.379354 | 0.213933 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147953640 | GTTGTTTGTTTTCTC[-/TCTTT]TATTTCCTAATCATT | 79658 |
| rs137889920 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148011593 | TCATATATAGTTCAC[A/T]TTCACATCAGCTATT | 79658 |
| rs137952196 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148016136 | TTATTATTTGAGATC[A/C]TAGGAATATACAAAC | 79658 |
| rs137954783 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147943189 | ATCAGAGTGGAAGAA[C/G]AGGAAATTGTGAGAA | 79658 |
| rs137960529 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147976210 | CTTACAGCATGCTTG[C/T]CATTTAATGGGAAAA | 79658 |
| rs137963850 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147946512 | TCCTAGGAAACTGCA[A/G]GATTGTGGTTTGCCC | 79658 |
| rs137967998 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148054243 | TTCAAACAGGCCTGG[A/C]CTTGCATCCACGTTC | 79658 |
| rs137970529 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147899736 | GGAAAAAATGCATGA[G/T]TCATAGATTTATACT | 79658 |
| rs137972221 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147789923 | TATGAGGGCTCACAT[C/T]GGAACCTTTCCTATT | 79658 |
| rs137976507 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147870078 | TTGAGAGGGAGTCTC[A/G]CCCTGTCACCCAGGC | 79658 |
| rs137991707 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147934665 | AACATAGTGAGACCC[A/G]CTCTCTACAAAAAAT | 79658 |
| rs137992754 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147852338 | CTGTGCTGGCCGTTC[A/C]CTTGTGCTCTGACAG | 79658 |
| rs138002789 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147749727 | AGGATAAAATCCAAC[A/G]TAAGGATTTGACAGT | 79658 |
| rs138010230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148007443 | CAGGTCAGCTTGACA[A/G]GATTGCTCAGTAGCG | 79658 |
| rs138023092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147776221 | TTTTGCGAATGAATG[A/G]TGGAAAAAAAAATTC | 79658 |
| rs138051329 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147804817 | CCTTTGCCCACTTTT[A/T]AATGAGGTTGTTTTT | 79658 |
| rs138067393 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148048541 | AAAATTCTGTTTCAC[C/T]GTAGTACTACAAGCA | 79658 |
| rs138076163 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148010410 | TTTTTCATCTATATC[A/C]TTAGAATAAAACTAT | 79658 |
| rs138079137 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147779946 | CCTTATAGTCTTGCC[A/C]GAGTATGAGTGGGAC | 79658 |
| rs138079760 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147965684 | AAAGAAAATGAAGGT[C/G]AGAAGATACTGTGAT | 79658 |
| rs138089307 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147969853 | CTTTCTGTGGCTAGA[C/T]AGTTCTATGAATGCA | 79658 |
| rs138093786 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147814654 | CTATATTTGCTACCA[A/T]AATGTTTGAATAATG | 79658 |
| rs138095074 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147929456 | TATCTTGGAAGAGTA[A/T]CTTTGTGTATGAACC | 79658 |
| rs138110063 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147744963 | GGAGAGGGTCAGGGC[A/G]AATCCGGAGGAACTC | 79658 |
| rs138111023 | in-del | -/AT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147833802 | TGATTAGATTCAATG[-/AT]ATATATATATTAAGT | 79658 |
| rs138123466 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147801130 | CTTAGATGTTGGAAT[C/T]TTAAAAAGCAATGAA | 79658 |
| rs138132405 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147845804 | TGTGTGTAAATTCAT[A/G]CACTGTGAAAACGTA | 79658 |
| rs138141541 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148032739 | AAGTCCCAAAACCTC[A/G]AAAGTAGGGAAGCTG | 79658 |
| rs138150162 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147992340 | AGTCACACTGACCAC[C/G]CCTCCCAGATCTGCT | 79658 |
| rs138165222 | in-del | -/GT | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147935784 | TCGAACAAGACTTGA[-/GT]GTATGTATTTTACGT | 79658 |
| rs138165776 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147887050 | GCGCGAGTCACCCTG[C/T]CCGGCCCATGCTATG | 79658 |
| rs138184890 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147850490 | CCATGAACCCAGCGG[A/G]AGGAACAGACAACTC | 79658 |
| rs138191356 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147775645 | CAGGCTTTTTGGCTA[C/T]GCTGACCTGGTTTTG | 79658 |
| rs138199589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147764137 | CCTGGAAGGTAGGAC[A/G]TGAGCAAGTTTCTGA | 79658 |
| rs138230584 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148004914 | ATATAATAAGAGTAA[A/G]CATTTTGTTTTCAGC | 79658 |
| rs138230866 | in-del | -/C | 0.122064 | 0.214785 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147807187 | TGAGGTCTGTTCCCA[-/C]CCCCCAATTCATGAA | 79658 |
| rs138261309 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147999782 | AGCGGCTGGTCACCA[C/T]CTTGGGAGCTCTGGG | 79658 |
| rs138271859 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147956856 | TCATTAGTATTATTA[C/T]GCCCCATAACTGATG | 79658 |
| rs138292857 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147879065 | GTGAGCCACCGTGCC[C/T]GGCCTCCCCTCTTCT | 79658 |
| rs138295972 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147954789 | GAAAATGCTGTGTAT[A/G]TTTTTAAAGTTGTCA | 79658 |
| rs138298014 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147987050 | TTGAACTGAATCACT[A/G]AAAATAGAATATTTT | 79658 |
| rs138298973 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147738273 | TAGAAATTGTAGGGC[C/T]GGGCGCGGTGGCTCA | 79658 |
| rs138299744 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148037378 | TCTTTGGATGTCCTT[C/G]TTAAAACAGAATGCC | 79658 |
| rs138301478 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147943576 | AAAAAATGACCAGTG[C/G]TTACGTAAGCGTGAA | 79658 |
| rs138303414 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147865419 | ATTTGAGACAATTTT[G/T]TGAGTTACTCTAACA | 79658 |
| rs138317566 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147757869 | CTGGTGCCCATCCCT[C/G]TCCAGTCACCTGTGA | 79658 |
| rs138326033 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147831866 | TAGGCAGGAGGCCTG[A/T]CTCCTTCTTGGACCC | 79658 |
| rs138334537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147959880 | AATCCTAAAGTATTT[A/G]AACTAGGTTTTCACT | 79658 |
| rs138356839 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147918724 | GAAATTTAATTCACT[A/C]TCACTGGGAGTAGCC | 79658 |
| rs138383438 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147837568 | AAGAGCCTCACTGCC[A/C]TGTGGCTGTTGGAAG | 79658 |
| rs138384850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148062097 | GTAGGCTGCTGGGGC[A/G]GGACGGCCCCTGGTA | 79658 |
| rs138388284 | snp | A/G | 0.000346024 | 0.0131488 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147881844 | TATTTGCAGGGGGAC[A/G]GAGAGGTGTTCTTTT | 79658 |
| rs138394532 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147794846 | TTCTTGTGGTGTTCT[A/G]TCATGTAAGTATAGG | 79658 |
| rs138412597 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147922240 | TAGGAATGGAGAGTG[A/G]AGGGAGGGAGGGAGG | 79658 |
| rs138416532 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147939120 | TCAAAAATGTCTTTT[C/T]GTCATTGATTTGTTC | 79658 |
| rs138425480 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148010723 | GGCCCGTAGTCCAAC[A/G]CATTGACATTAACTG | 79658 |
| rs138447480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147826491 | ACACCTGCTGGAAAG[C/T]AGGACGCTGTCCAAA | 79658 |
| rs138447758 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147796896 | TAATGTAAAAACCTC[A/G]TTCTTGTCTTTTCCC | 79658 |
| rs138448571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148030389 | AACATCTTTTCAAAC[C/T]AACCAAAGTATTGTT | 79658 |
| rs138450281 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911371 | ATTTTTGTTGTTGTC[A/G]TTGTTGTTGGAGACA | 79658 |
| rs138455948 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147914905 | GCAGCCATTCCAGCA[C/G]ACTTTGGAGATACTA | 79658 |
| rs138463402 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147809648 | ATCATTGCACTATAC[C/T]GTACACCAGCGGTCC | 79658 |
| rs138474186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147895134 | ATCCCAGTAATGTTT[C/T]ACAGTTTTCAGCATA | 79658 |
| rs138485602 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147790782 | TTTGGATGAAATATT[C/G]TAAACATAGTACATA | 79658 |
| rs138489394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147871608 | AGACAGTGTCCTACC[A/G]TATAGATTATTGTGA | 79658 |
| rs138491990 | in-del | -/T | 0.0298908 | 0.118541 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148032802 | GAAAGCCCACTGGTG[-/T]TAAGTCCAGGAGTCC | 79658 |
| rs138513638 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147749950 | TCACTTAACCACAGC[C/G]AACAGTGTTTTGTTT | 79658 |
| rs138514640 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147793742 | CCTCCTCTGCTGAGG[C/T]GCCTTGCAGAAACAA | 79658 |
| rs138517590 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148016525 | AAAAAAAAAATTGAG[A/G]GAAAAAATGCAAATT | 79658 |
| rs138530554 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147733522 | CTCACCTAGATTCTC[A/G]GTTCAGTAATTCTCA | 79658 |
| rs138543499 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147875552 | AGGCACACACATTCA[C/T]TCATACACACGTATA | 79658 |
| rs138568740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148046480 | TATTATGCACTAAAT[A/G]GCAACTGAGAATGAC | 79658 |
| rs138576653 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147752795 | GCCTCCCAAAGTGCC[A/G]GGATTACAGGCGTGA | 79658 |
| rs138622288 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148006785 | CAGTGAGAACCTGCC[A/T]GGTGATTAGTTACCC | 79658 |
| rs138625638 | snp | C/G/T | 3.29817e-05 | 0.00406078 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148064442 | GGAAGGCTCGAGCCG[C/G/T]GTATCCGTGTGAAGC | 79658 |
| rs138632418 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147976984 | AAGAACTTCGTAATA[C/T]TTATAATAATGAGAA | 79658 |
| rs138646472 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148020241 | GCAAGGTTCAAGGAA[C/T]TGATTATATATGTAC | 79658 |
| rs138651953 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147970491 | AGGCCTATGTGTGTC[A/G]CTGACAGTGGCTCTG | 79658 |
| rs138656417 | snp | A/G | 0.000165017 | 0.00908191 | synonymous-codon, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147965055 | ATCTCGTGTTAATGC[A/G]ATCCATTTCTTGGTA | 79658 |
| rs138657292 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148048877 | ATTCATACGCATTTT[A/G]AAATGTCATGAAAAG | 79658 |
| rs138660041 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147890602 | GAGGCCGAGGTGGGC[A/G]GATCACCTGAGGTCA | 79658 |
| rs138671003 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147778964 | CTGTGAACTAAGGTA[C/G]TGAAAAGGAAAGTAG | 79658 |
| rs138677200 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147741271 | CTTTCAAAACAGTCA[A/G]TAATTAATAAATCCA | 79658 |
| rs138684964 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147906186 | TTCCATTTCTTGATA[A/G/T]ATACCTGAAAGAATT | 79658 |
| rs138689488 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147768050 | AATGGACTATTCCGG[C/G]ATGACTTTTAAATAT | 79658 |
| rs138695294 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147981944 | CCTTTACTTTGAGCC[A/C]AGGGGCGTGATCATA | 79658 |
| rs138699021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147846473 | GATGAATATTTTCTT[C/T]TATTTGCATTTTCAG | 79658 |
| rs138717577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147858829 | TCCCCAAGTGAATTT[C/T]CAAATCCACTTCACT | 79658 |
| rs138719462 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147929542 | TTAAACAGACATTTA[A/C]ACATTAGTGCTTACT | 79658 |
| rs138722125 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148026496 | TTCCATCGGCATTGG[C/T]GCATCTAGCCATACT | 79658 |
| rs138729218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147863045 | ATGTGTTTCAAATGT[A/G]TTAAATGCTTTTCAA | 79658 |
| rs138734254 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147934445 | CATATGGGGATATGA[C/G]CAGGTTACTTTCTGT | 79658 |
| rs138741790 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147839856 | CATCCGAATGTCTGA[C/T]GAAAAAGGATTTCAG | 79658 |
| rs138760567 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147804066 | GTAAACTGTGTGTCA[C/T]GGGGGTTTGGTGTAC | 79658 |
| rs138780126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147738867 | AATTTTGATTGTAGT[C/T]CGGGATGCTGGAAAA | 79658 |
| rs138793641 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147807503 | TGAAATGGTCAGGAA[C/T]GTAAAGAGGTCGGTG | 79658 |
| rs138802500 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147745427 | GTAGACCCAGATTAC[A/G]TGGTCAGTGGGAGAG | 79658 |
| rs138890648 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148069210 | AGCCTTATCTGCAAC[A/T]GCGGAGCCACTTTTC | 79658 |
| rs138895275 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148020759 | GCAGCAAACATACTC[A/G]TGCGTGTATCTTTAT | 79658 |
| rs138903194 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148038742 | TTCAGGCACAAGGGG[A/T]TATAGGGGCATGAGG | 79658 |
| rs138909501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147836081 | GTGTTTGATTTAAAT[A/G]ATCTGAATAAAATTT | 79658 |
| rs138915084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147749150 | AATTTTAACCATAAT[A/G]GAGGAGGTGAGAGAG | 79658 |
| rs138923719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147906565 | AAAAAAATGGTTACA[A/G]CAGTTAAATCTTAGG | 79658 |
| rs138941943 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147794758 | GAGACTGAGATGTTA[A/C]AGTAGCCCAGGATCA | 79658 |
| rs138942631 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147991988 | ACATTCAAAAAGTGC[A/G]GGATTAACTTCAGTG | 79658 |
| rs138976791 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147871820 | ATTTAAAAAATAGTG[G/T]CTGGGGATGGTGGCT | 79658 |
| rs138983049 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147946975 | TAGGAATTAAACACT[A/G]TGAAACAACTCGTCG | 79658 |
| rs138989309 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147950421 | TCTGGAGCCAGCCTG[C/T]CTGCCAGGGTTGGAG | 79658 |
| rs139003756 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147742737 | TGATCCGCCTCTCTC[A/G]GCCTCCCAAAGTTCT | 79658 |
| rs139018807 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147827475 | CCCCTAAGCTTGTGG[A/C]TGTTAGGAAAGGGTT | 79658 |
| rs139019261 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147996228 | ATGGCCTATGGAAAC[C/T]TCTATCATAAACACC | 79658 |
| rs139020298 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147967490 | CCTGGGGTGTGGTGG[A/T]TGGGGTTGACCCAGG | 79658 |
| rs139021161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148044946 | GAAGCGCTGTGGAAA[A/G]AGTGGCTTCACTGAA | 79658 |
| rs139064406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147843486 | ATTCTTTCTTTAAAA[C/T]GTCTCTGCAGCCCAC | 79658 |
| rs139083187 | snp | C/T | 0.00151493 | 0.0274803 | synonymous-codon, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148046929 | GGAGGACACCCCTAC[C/T]AGCAGTCTGGACTCA | 79658 |
| rs139087699 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148000034 | TGCACCTATTAACTG[A/G]TCATTTACATTAGGT | 79658 |
| rs139094970 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148001294 | gttttggtaccagta[C/T]catgctgttttggtt | 79658 |
| rs139096067 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147928358 | CACAGCCACCCTTAC[C/G]TGCCAAACTGTCTGG | 79658 |
| rs139097803 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147880509 | CTGCTTAGTGATATC[A/T]TTCTGTTTTAGCCTC | 79658 |
| rs139127657 | in-del | -/CTAA/CTAAGC | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148003893 | GTCTTTTATCTGAGT[-/CTAA/CTAAGC]GTAAGCCTAAATCAG | 79658 |
| rs139132168 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147739079 | GTAATCCTAGCTTCT[C/T]GGGAGGCCGAGGCAG | 79658 |
| rs139140377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147961398 | GGATTGTCTCTTTTT[C/T]CCCTGATTGGTTTGT | 79658 |
| rs139143326 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148039058 | ACCCACCCCCACCAT[G/T]TTGGTATTTTCCAGA | 79658 |
| rs139143454 | snp | C/T | 1.66164e-05 | 0.00288235 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147847177 | AACTGAAACCCTGAT[C/T]AAACCCTTGGAAAAA | 79658 |
| rs139150580 | snp | C/G/T | 0.000708483 | 0.0188082 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148023345 | CGCCACCAAGGCAGT[C/G/T]GAAGAGACAAGGCCA | 79658 |
| rs139150968 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147883023 | ACAAAAGTAATTAAT[A/G]CTGCTTCCTCTCTTA | 79658 |
| rs139153936 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147800793 | TCTATGCTGTCTTGT[A/G]CCTTGTCATTCATTA | 79658 |
| rs139155111 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147799641 | GTTACTGTACTTTTC[A/C]GTTGTATAATTTATA | 79658 |
| rs139162341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147885884 | TGAACTGCTTCTAGA[A/G]TGTTTAGCTCCCTAA | 79658 |
| rs139166974 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147919517 | CTTCCTAAAGCAGTT[G/T]TTCCCAAACTTTGCT | 79658 |
| rs139172340 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148004212 | AAAAATTGACTTAAG[C/T]TTTGAAGGGCATCTC | 79658 |
| rs139184157 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147985045 | CCTCACCTGGTCTCA[A/C]GTTCTCTGCATGAGG | 79658 |
| rs139195773 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147795544 | AGCAGTTTACAAACG[C/G]AACTTCTGGAGTGTG | 79658 |
| rs139214083 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147762967 | AACAAAAGACTTTTA[C/T]GGTTAAGGAGACAGG | 79658 |
| rs139216797 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147888439 | AGTGGGAGTGGGGGT[A/G]GTTACATTCCTCTAA | 79658 |
| rs139234121 | in-del | -/T | 0.104149 | 0.203046 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147894606 | TTGCACCAAGAAATA[-/T]TTTTTTTTACTCTAT | 79658 |
| rs139284992 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147873073 | TATTTCCTAAGGCTG[C/T]CTGCTGAGAAGTCCT | 79658 |
| rs139292633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147978836 | AACAATTTTTTCATA[C/T]GTTTTTTGGCCATTT | 79658 |
| rs139300864 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147792061 | AATTGCTGTGTGGTA[A/G]CACGTGAGCGTCTTT | 79658 |
| rs139301468 | snp | C/T | 0.262159 | 0.249704 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148002419 | gtatcaagatgatgc[C/T]ggcctcatcaaatga | 79658 |
| rs139305144 | in-del | -/CG/GC | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147741801 | CACACGCACACACAC[-/CG/GC]ACACACACACACACA | 79658 |
| rs139308913 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147751840 | AGGGTACTCATCTAG[A/G]TAGCTGAGGCTCCTG | 79658 |
| rs139316557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148062553 | GAGGCCATTCCAGGT[A/G]TCTGTTCACTGACCT | 79658 |
| rs139320056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148058129 | ATATACAGATCTACA[A/G]TATTTCCTTCTGTCT | 79658 |
| rs139330893 | snp | A/G | 1.6507e-05 | 0.00287284 | synonymous-codon, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147879281 | CTATTGCATGTATCG[A/G]AAAGCAGCAAAGAAG | 79658 |
| rs139331147 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147767178 | AAAGCAAATCCAGCA[A/G]CAAAGAAATCTGTTC | 79658 |
| rs139337846 | in-del | -/TATCTATC | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147839093 | TGTTTAGATCTATCG[-/TATCTATC]TATCTATCTATCTAT | 79658 |
| rs139337991 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147838572 | ACAGGGTCTAACTGT[C/T]GCTTGGGCTGGAGTG | 79658 |
| rs139342380 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147765636 | CAAAGCCTGTCTTTA[C/G]AAAAAATACAAAAAT | 79658 |
| rs139385847 | in-del | -/T | 0.0839998 | 0.186933 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147970577 | TCCTCCCTAAGAATG[-/T]GAAAAATGTTGACTC | 79658 |
| rs139400620 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147840442 | TCCTAAACCTTTTTA[A/G]CATTCTGGTTACATT | 79658 |
| rs139414418 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147746143 | AGAGTCTCACTCTGT[C/T]GCCAGGCTGGAGTGC | 79658 |
| rs139421900 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147816099 | AAGACAGTTGGAAAA[C/T]GAGTGGGCTAGGTGG | 79658 |
| rs139422289 | snp | A/G | | | upstream-variant-2KB | ARHGAP10 | GRCh38.p7 | 4:147730807 | CCTAGTGGGTGCCCG[A/G]CACATAATAATTGCT | 79658 |
| rs139426902 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148050524 | TTCTACAGGCGCCCA[C/T]CACCACGCCTGGCTA | 79658 |
| rs139446897 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148064608 | CTGTTGTCGGGAGGG[C/T]GAGTCTCCCCCTTGA | 79658 |
| rs139455833 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147930950 | CACCTACAGGGACAG[C/T]GGATGCCTGCTAGTG | 79658 |
| rs139458475 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148005363 | TTGAGGCAGGAGGGC[A/C]ACTTGAGCCCAGGAG | 79658 |
| rs139475713 | in-del | -/G | 0.00400158 | 0.0445509 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147920342 | GAATGGTGTGAACCC[-/G]GGAGGTGGAGCTTGC | 79658 |
| rs139476251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147802642 | GCCAGCTCTGCTTCG[C/T]AGGAAACCAGCTCTG | 79658 |
| rs139483950 | in-del | -/CA | 0.0402882 | 0.136092 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147821231 | GAGGCTCTGAATTGG[-/CA]CAGTGTCACTTTCTC | 79658 |
| rs139488532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889180 | TCTTCTGCACCACAC[C/T]GCTATACTGTGAGCT | 79658 |
| rs139493903 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147810539 | AACGTTTACATCTCA[C/T]CTTTAATACAAATTC | 79658 |
| rs139503260 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147896080 | CTACTTGGTCATGAT[A/G]TACTAGCTTTTTGTA | 79658 |
| rs139516358 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148069562 | CATCCTGTCTTTTAT[G/T]AATACCGAGTCTGTG | 79658 |
| rs139527160 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148018043 | ACTCTTAGGAGACCC[A/G]AGTAAGCAAGCACTT | 79658 |
| rs139557083 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147772417 | TTTTAAGCCACAGTT[A/C]TACAGACAGATGGGA | 79658 |
| rs139562390 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147944781 | TACTTTCTCCTTTGC[A/G]TAGTAGGTGTGTAGA | 79658 |
| rs139576376 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148070555 | CCATGAACTCAATTC[A/G]CTGAGTTGCAATTAG | 79658 |
| rs139588840 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147947736 | AACCATACATAGGGT[G/T]GTTTTTCAGGTAAAA | 79658 |
| rs139593086 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148021762 | TTTTTAGGCAGATAA[A/G]TAGTTTGCTATTGGC | 79658 |
| rs139593535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147957969 | TAATGTAACTTTCTC[C/T]GTTAGCTGAATTCCA | 79658 |
| rs139593618 | snp | C/G | 0.0178098 | 0.0926698 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147882304 | TGTCTCTACTAAAAA[C/G]ACAAAAAAATTAGCC | 79658 |
| rs139599714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147833582 | AGTGATTCAGAGGAG[C/T]TGGACTTTGAAGAAG | 79658 |
| rs139612359 | in-del | -/TAAT | 0.0185938 | 0.0946107 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147768588 | TTGAACATAATGAAA[-/TAAT]TGTTCATTTTTCAAA | 79658 |
| rs139637969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147822513 | CATTTTTTCAGCATC[C/T]GTTCTGTGGCAGGGT | 79658 |
| rs139644149 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148019149 | AGCCTGTTACTTGAT[A/G]TCCTTTTCCAGAGCA | 79658 |
| rs139655520 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147993618 | CATGGTCTGGAGATC[A/G]TCTGAGTTTGGACCT | 79658 |
| rs139667446 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147996565 | GTACAGCCCAGTCAG[A/G]GGAGTGAACACAGCT | 79658 |
| rs139667788 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147948694 | GGGCGCGGTGGCTCA[C/T]GCCTGTAATCTCAGC | 79658 |
| rs139674812 | snp | A/G | 0.00151635 | 0.0274932 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147906733 | CTGTAAGAATAATCA[A/G]TGGTTGAGTTTTATT | 79658 |
| rs139722691 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147951681 | TGGTCTTAAACTCGT[C/T]GTCTCAAGTGATCCT | 79658 |
| rs139725305 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147780962 | GAGAATGAGAGAAGA[C/T]GCTCCAGAGAATGAG | 79658 |
| rs139730142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147952081 | ATGTTGTAGCACATA[C/T]CAACAGTTCATTCCA | 79658 |
| rs139757477 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147786416 | CTGAAAAGCAGCTTA[G/T]TTCTTAGCAATGGCA | 79658 |
| rs139768682 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147829276 | CCAGGTTGGTCTCGA[G/T]CTCCTGACCTTGTGA | 79658 |
| rs139769653 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147755148 | CAATAAGGATATAAT[A/G]AAAGCAAACTTATTA | 79658 |
| rs139778776 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147786738 | CAACAGTGATTACTA[C/T]CTTGAACCTGTAAGA | 79658 |
| rs139783572 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147829484 | GTGAGCCACCGCGCC[C/T]GGCCAGGACAGTGTT | 79658 |
| rs139815372 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147962614 | CCCCCATCATAAATC[A/G]TAGGGCATCTATATT | 79658 |
| rs139816471 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148040577 | AAACTCCTGGCCTCA[A/G]GTGATCCACCTGCCT | 79658 |
| rs139844890 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147839118 | TCTATCTATCTATCT[A/G]TCTATCTATCTATCT | 79658 |
| rs139847871 | snp | A/C/G | 6.09853e-05 | 0.00552174 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147966884 | TGTTTTCGGCTTGTC[A/C/G]CCATGTACTACACAA | 79658 |
| rs139864323 | in-del | -/C | 0.0178098 | 0.0926698 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148018525 | AGTGTCCCTTTAAGT[-/C]ATTCCTGGTGTTTCA | 79658 |
| rs139865910 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147897601 | TAATATCTGCCTTCT[C/T]AAAAATAAAGACCCT | 79658 |
| rs139874316 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147973678 | ATCCCTGCTCCCCCC[A/G]CCACTGCTCACTACC | 79658 |
| rs139877845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147841005 | CTTGCTTCCTCTTTT[C/T]GTAAGTCAAGTTTCG | 79658 |
| rs139887969 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147880876 | TAGTCACATATTTTT[-/T]GTGACATGTGGTAAG | 79658 |
| rs139937487 | in-del | -/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147838689 | GATGCATGCCACCCC[-/C]ACCTAGTTAATTTTC | 79658 |
| rs139956461 | snp | A/G/T | 0.000214432 | 0.0103526 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147913127 | AAATGCATCAGTGCC[A/G/T]TTGAAACACGAGGTA | 79658 |
| rs139958661 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147734591 | TATCAAAGACTAAGA[G/T]CCTTGGACTAAAGTC | 79658 |
| rs139988349 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147780440 | GTGGAGGAGGGAGCC[C/T]GGTCAGCAGGCTTGA | 79658 |
| rs139990305 | snp | A/C/T | 0.00458098 | 0.0476408 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147857643 | AAAAAGAAAGACTCA[A/C/T]ATTTACAAGAGGTAT | 79658 |
| rs140025332 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147984772 | TGGGTTAAGAGCCAG[C/T]TGTGGCCAATATAGT | 79658 |
| rs140032777 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148063782 | ACCAGTGAGGTGAGG[C/T]GTTTCCTTTGGATTT | 79658 |
| rs140050359 | in-del | -/T | 0.222035 | 0.248431 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147747647 | GTGTCCTGTTTTTTT[-/T]GTGGAAAGGATAGAG | 79658 |
| rs140051470 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147860825 | CAAATTGAAATTGTG[C/T]ATTTGTTAAAAACTA | 79658 |
| rs140058142 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147988856 | CTTTCCCCACCTGGG[A/G]CCAGCCACCAAGGAA | 79658 |
| rs140062252 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147940474 | CCCCAGACATTATGT[C/G]AATGACAAAGCGCTT | 79658 |
| rs140070735 | snp | C/G | 0.0248432 | 0.108648 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148008891 | CAGAGAGTCCGCTGT[C/G]TACTGTTAAGTCGGA | 79658 |
| rs140083257 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148012756 | ATGTATAACCAGGGG[C/T]TGAATAAATTCTAGG | 79658 |
| rs140084924 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147967849 | CTTGTAAGTGGCTGC[A/G]TAGCCATGCGTATTC | 79658 |
| rs140093829 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147953561 | GCTCATAGTATTTCT[G/T]TATTTTATTTTTAAT | 79658 |
| rs140111269 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148029349 | ATAGCTCACATTCAC[A/G]GCAGCGGTGCACTCT | 79658 |
| rs140111606 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147746483 | TTGGCTCACTGCAAC[A/C]TCCACCTCCTGGGTT | 79658 |
| rs140111707 | in-del | -/TGG | 0.0372196 | 0.131242 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147917209 | GGTAATTGGGCCTGA[-/TGG]CATTCTTCAGAGTGA | 79658 |
| rs140138947 | snp | A/T | 0.0205511 | 0.0992634 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147896677 | TCAACTTTGGATTTA[A/T]TTTTTCTTTTCATTC | 79658 |
| rs140142578 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147817279 | CGAGGGCTCAGGCTT[A/G]TAACTTAAGGGGTTA | 79658 |
| rs140145161 | in-del | -/T | | | upstream-variant-2KB | ARHGAP10 | GRCh38.p7 | 4:147730876 | TTAGTGTTTTTTTTT[-/T]AAGAAATACTTTTTT | 79658 |
| rs140167863 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147913817 | GGTTGAAGCACTCTG[A/C]AGATACTCTCCACCC | 79658 |
| rs140175277 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147821172 | CGTGAAGGACTGAGG[G/T]TTCCATGAGAGTGGA | 79658 |
| rs140180223 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147750333 | ATTTCTTTCTGACTG[C/T]GGCGTCAGTTTAATG | 79658 |
| rs140183055 | in-del | -/CTTTTTTTTTTTTTTTTTTTTTTT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147969323 | GAAGTTTTGTTTTGC[-/CTTTTTTTTTTTTTTTTTTTTTTT]CTTTTTTTTTTTTTT | 79658 |
| rs140206114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147849079 | CACCTGTGAAGAGCC[C/T]GTCATTGTAGGTCAT | 79658 |
| rs140213720 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147773434 | CTCCATAGCAAAGGG[G/T]CCATGGAAGGCTCTG | 79658 |
| rs140216761 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147789872 | CAGGATGCAGATGAT[A/G]TGTGGGAGTCTCATC | 79658 |
| rs140222359 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147875628 | AAGAGGGACATATTA[C/G]TATTTTTCTTCTTCC | 79658 |
| rs140222992 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147921082 | AGGGTTCTGCTTAGG[A/G]TGCAGTATTTATAAG | 79658 |
| rs140226234 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147793921 | TTCAGCACCTTAAAA[A/G]ATAAAGTGTAGAAGG | 79658 |
| rs140229042 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147998766 | AAATTTACATTAATT[A/C]GTGATACCATACTTC | 79658 |
| rs140229379 | in-del | -/AAAAC | 0.0162398 | 0.0886349 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147876605 | CTCAAAAAAAGGAAA[-/AAAAC]AAAACAAAACAAAAA | 79658 |
| rs140230604 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148015620 | TCAAGGACAGAGAGT[C/T]GGAAAAGGTTTTCAT | 79658 |
| rs140257308 | snp | C/T | 0.030665 | 0.119967 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147878242 | CTGGGACTACAGGCG[C/T]GTGCCACCACGCCTG | 79658 |
| rs140259588 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147796470 | AGGTACATAATTCCT[C/G]CTCAGTCTGGTACCC | 79658 |
| rs140267191 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147756225 | AATACCTCATGGGCC[A/G]CAGTTCTTAATTGCT | 79658 |
| rs140291289 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147975582 | AGGACAAGAGAACAT[G/T]TGAAAAAGGAGTGAC | 79658 |
| rs140330689 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147776942 | TCCTACGAGAGAGCG[A/T]GTCTTTCCTTCCTGG | 79658 |
| rs140332537 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147736312 | ATGGTTTTTGCTTTG[C/T]TCCTCTTAGGAAAAA | 79658 |
| rs140352641 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148060668 | CTTGCACGTTGCCCC[A/G]TCTTGTGAATATTCC | 79658 |
| rs140353508 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148007026 | AGGATGTAGAAAAAT[C/T]AGACGAAATTGCCTG | 79658 |
| rs140371963 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147908024 | ATTTTTGTAATTTTT[A/T]GTAGAGACAGGGTTT | 79658 |
| rs140377296 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147937560 | TTTATATTCCTTTGG[G/T]TATATACCCAGTAAT | 79658 |
| rs140401527 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147781841 | AAGTACATCTTTACG[C/T]GTCAGTATTTCCATA | 79658 |
| rs140410379 | in-del | -/AT | 0.0513262 | 0.151752 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147740902 | CCCAAGGGGTAGGAC[-/AT]CTATCTCAGATCTGG | 79658 |
| rs140414169 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147742514 | TTGAGATGGAGTCTC[A/G]CTTTTGCAGCTCAGG | 79658 |
| rs140420687 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148048496 | ATTACTAGGTATGCT[C/T]GTCACCTTTACTCTT | 79658 |
| rs140437631 | snp | A/C/G | 0.00438476 | 0.0466401 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147861893 | CCTGGAAAAAGCACC[A/C/G]TAAGTTTTCATCCCA | 79658 |
| rs140444430 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148010214 | TAATAACATGATGTT[A/G]GAGATTCCAGATATC | 79658 |
| rs140446818 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147929232 | TACCCTGCTGCTTGG[A/C]AGTATTTAATGCACT | 79658 |
| rs140460724 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147744874 | GATTCTGGAGACACA[C/G]CATATGGATGGGAAA | 79658 |
| rs140467446 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147845723 | AGTTGGGTAGATCCA[G/T]ATGTGGGAGCTTAAA | 79658 |
| rs140490244 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147941475 | AAAATTCGTGACCTG[A/G]AAAACTGTTTTTACT | 79658 |
| rs140490342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147894517 | CCTATCTTTTTCTTC[A/G]GTGTCTTTTGATGAG | 79658 |
| rs140492441 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147807904 | ATGAAGGTCCTCGTC[C/T]TCCTTTGGTTGTATG | 79658 |
| rs140503814 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148027438 | GCTAACTGCAGCACA[C/T]TTTGTTGAGCATGTG | 79658 |
| rs140510806 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148014100 | GAAGAGGAGAAAAAA[A/T]GGAATGTTGTGTATG | 79658 |
| rs140527096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148043096 | CTAAAACCAGGTTAT[A/G]AAACCAGTATATGAT | 79658 |
| rs140550063 | snp | C/T | 0.0106973 | 0.072348 | synonymous-codon, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147913126 | AAAATGCATCAGTGC[C/T]GTTGAAACACGAGGT | 79658 |
| rs140556720 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147921225 | AGGATAGGAATTCTG[C/T]AAGGAATTTTACCTT | 79658 |
| rs140557280 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147898840 | ATGGGGTGGGGTGGG[A/G]TGGGTTGAGGAACTG | 79658 |
| rs140559133 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147813507 | AAAGCCGTGGGAGCC[A/G]AAATTGAAAGAATGC | 79658 |
| rs140559891 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147999532 | CTGATCCAGTGAGGC[A/G]CCCATTGCCGCTCTG | 79658 |
| rs140562857 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148025291 | ATGTTCATTATTTGC[A/G]TGATGTTTTGTTCTA | 79658 |
| rs140564298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147916123 | TTGTACACTTCTTGA[A/G]TCTATGTGACTGATG | 79658 |
| rs140565945 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147805781 | ATCACACCACTGCAT[C/T]GTGGGCAACAGAGCA | 79658 |
| rs140567157 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147740232 | CTGGCTACGTTTTGT[A/G]TTTTTTGTAGAGATG | 79658 |
| rs140569334 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147774419 | GCCTGTAAGAGTGTG[C/T]AGGTGGAAAACATGA | 79658 |
| rs140577889 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147796727 | AGACGGGGTTTCACC[A/G]TGTTAACCAGGATGG | 79658 |
| rs140583860 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147992693 | TTACAGACGTGAGCC[A/G]TTGCACCTGGCCGAA | 79658 |
| rs140624201 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147777395 | TCCCTAGTAGCTGGG[A/C]CTACAGGCACCCGCC | 79658 |
| rs140627994 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147873813 | TCAGGAGGTTGAGGC[A/T]GTGATGAGGTATTAT | 79658 |
| rs140629700 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147918971 | AGAATTAGAAATTAC[A/G]TAAGATTGGACTCAT | 79658 |
| rs140629929 | snp | A/T | 0.02016 | 0.0983543 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147792990 | TAAAAATACAAAAAT[A/T]AGCTGGGTGTGGTGA | 79658 |
| rs140645848 | in-del | -/A | 0.0162398 | 0.0886349 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147736052 | TTTTTTAAAACTAAC[-/A]GTCCTTACAGTTATT | 79658 |
| rs140713350 | snp | A/T | 0.25801 | 0.249872 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148001444 | agttttttccaattc[A/T]gtgaagaaagtcatt | 79658 |
| rs140716288 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147994598 | CTCAAAATGTAGATC[A/G]TAATCTCAATGTTAT | 79658 |
| rs140736730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148030309 | CTGAATTCAAGCAGC[C/T]GTCACTCTCTTTATA | 79658 |
| rs140745261 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147876638 | AAACCACCTCGATAG[C/T]CTTGAGAATGTTAGA | 79658 |
| rs140751490 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147751935 | TCTGCCATCAGGTTG[C/G]AGTGCAGTGGCATGA | 79658 |
| rs140762201 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147949421 | GAACAGTGTTTCTCA[A/G]CTGAGGATGGTTTTG | 79658 |
| rs140769099 | snp | A/G | 1.6549e-05 | 0.0028765 | splice-donor-variant | ARHGAP10 | GRCh38.p7 | 4:148047052 | CTGGGCATCCACTAT[A/G]TAAGTAACCGTGCTT | 79658 |
| rs140787963 | snp | C/G/T | 0.0162398 | 0.0886349 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147752652 | TGTGCCTCAGCCTCC[C/G/T]GAGTAGCTGGAATTA | 79658 |
| rs140790669 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147980681 | GGCTTTTCTTGGTTG[A/G]TAGGTTTTTTAAATT | 79658 |
| rs140794450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147914345 | TCCTGTATTTGCTGC[A/G]TTGCATTTTTATTTT | 79658 |
| rs140799905 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148061077 | CCCACCCACCCGCGG[G/T]TGTTTTCATGGAGGT | 79658 |
| rs140808619 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147916556 | GCTCAGAATAAACTG[C/G]AGAACTGGCAGTGCC | 79658 |
| rs140809788 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147754555 | ATTTAGTTCCTTTGG[A/C]TGAATTTCTGTTGTC | 79658 |
| rs140820770 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147825826 | CCTGGCATCCTGAAC[A/T]TTGAGCGCATACCTA | 79658 |
| rs140848310 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147835137 | CCTACTATGAGCCAC[C/T]GTGTTCTCACACCTG | 79658 |
| rs140860373 | snp | A/G | 0.000759076 | 0.0194669 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148064427 | TCAGCATCCGCAGTC[A/G]GAAGGCTCGAGCCGT | 79658 |
| rs140864230 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147793651 | CCTGCCCTCACTTCT[C/G]AGGCTTCATGTGTAT | 79658 |
| rs140869159 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147945937 | CAAGGCCACCACACA[G/T]GAATTGAAGAGGTCT | 79658 |
| rs140893112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147819407 | CGATCTGGCAAAGCA[A/G]ACAGCAAAATAGAAT | 79658 |
| rs140901360 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148053364 | CCCTTGGTTTGAAGA[C/G]GGAGCACTGACCTTA | 79658 |
| rs140923247 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147903197 | CAGCAGGCTCATGGC[A/G]CCAGTGAGGAGGCTG | 79658 |
| rs140928613 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147931700 | AAATTCCAAGGCTAG[A/G]TGTGTTTTGGAATTC | 79658 |
| rs140928675 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148056940 | GCTTCAGGGCTTTAC[A/G]CCTATCATCTCATTT | 79658 |
| rs140932578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148006697 | ACATTTTAAAAAGAT[C/T]ATGTGTTTAAAGAAG | 79658 |
| rs140934292 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147934054 | AGCTCTGAGTTGGGA[C/T]CTTGGCTGAGGGGCC | 79658 |
| rs140940392 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147890477 | TCAATAATATATAGA[C/T]AAATAACAATGAAAT | 79658 |
| rs140959666 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148010460 | ATATTATCTTTCATA[C/T]CCTTTTTTTGGTTGA | 79658 |
| rs140992982 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147935401 | CTTTTTAGGGATTCC[A/G]TAATAAATGTGTGTG | 79658 |
| rs140993287 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148008518 | TAGGTAGAGGCCGGG[A/G]TGATGTTGAACATCT | 79658 |
| rs141044921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147805511 | ATTCTATGAAGAATG[C/T]CAATGGTAGTTTGAT | 79658 |
| rs141057837 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147774001 | GAGTCATTCCTGGCT[C/T]TGCCACTCCAGCTTT | 79658 |
| rs141071171 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147849656 | CCTGAAGCTCTTTCA[A/G]TTCCCTGTGCTTTTA | 79658 |
| rs141073482 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147835939 | ACAGAGGGAAGGAAG[A/T]TCAAGTTTCAGCATC | 79658 |
| rs141074622 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147762475 | GTTGATTGGGTAGGT[A/G]AACTAGCAAAAAAAA | 79658 |
| rs141076993 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147899230 | TACCTTTAAAATTTT[G/T]TTAAAATTCCACTGT | 79658 |
| rs141094025 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147737088 | TAAATGACATAAGAC[A/G]GTTTTGAGTTGGGTT | 79658 |
| rs141129371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148008443 | GGGACATTTGGTAGT[A/G]TCTAGAGACAGTTTT | 79658 |
| rs141139773 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147784713 | TAAAATATATATTAT[A/G]AATATAATATATTAT | 79658 |
| rs141144749 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147974821 | GCCTCACAATCATGG[C/T]GGAAGGGGAAAGGCA | 79658 |
| rs141145773 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147986011 | TTGAAGTGGATTTCC[A/G]TTTTCCTGTTTGAAT | 79658 |
| rs141147948 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148067039 | TCTCAGGAGCTCCTC[A/G]TTCTGTCCCTCCCCT | 79658 |
| rs141149502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147906361 | ATTAGGCTTTTATGT[A/G]GCAATTGAAAGTTAT | 79658 |
| rs141162728 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147967259 | GAAGGGATGTGAGAT[A/G]GGGCCAGAGGACCAT | 79658 |
| rs141171029 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147780269 | CGTGTCTGGATCAGG[G/T]CCGAGGCTCAGCATG | 79658 |
| rs141195119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147850552 | CACTGCAAAGGTCTG[C/T]GGCTTCACTCCTAAG | 79658 |
| rs141207224 | snp | G/T | 1.64879e-05 | 0.00287118 | missense, utr-variant-5-prime, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147822921 | ACGTGAATTTTCAAA[G/T]TTTTTGAAGAATCTG | 79658 |
| rs141208306 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147979476 | GTATTGTTTGAAGCC[A/G]GCTTTGTTCCTTTTG | 79658 |
| rs141244949 | snp | C/T | 0.000445063 | 0.0149109 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148064448 | CTCGAGCCGTGTATC[C/T]GTGTGAAGCAGAACA | 79658 |
| rs141258036 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147855861 | TTCCAGAAGAACAGC[A/G]TGTGGTCCCATGTGG | 79658 |
| rs141258774 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147990050 | GGGTCCCTGACTTCC[C/T]GCAACACTCCTGATA | 79658 |
| rs141262292 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147850684 | CACTGCGAGGGTCCG[C/T]GGCTTCGTTCTTGAA | 79658 |
| rs141262957 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147942897 | GAAAGAACATGCCCA[G/T]ATAAGCAGATGCCTG | 79658 |
| rs141265513 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147960563 | CTCTGCAGGATTTAT[A/G]CTTAAAATTTACCAG | 79658 |
| rs141270334 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147807263 | TGATTTTTATATGAA[A/G]TATCCTGCATAACAG | 79658 |
| rs141292691 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147775982 | TGGCTATGATGGCAC[C/T]GAGCACAAAGCCCAG | 79658 |
| rs141293067 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147740868 | GCTTAATGAAAGCAT[C/G]TTGTATACCCATTCT | 79658 |
| rs141299288 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147744535 | TTGTGCAAATGAATC[A/G]GAGGAAAGCAGGACT | 79658 |
| rs141305283 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147812086 | GAGGCAACCTCCTGA[G/T]GGGTGAGAGTTGCAT | 79658 |
| rs141314800 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147838090 | CATTTTCTGCACTTA[C/T]TTAATAAAAAATTTG | 79658 |
| rs141324122 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148031071 | CTCCAACAACAACAA[A/C]AAAAAAATGAATTTT | 79658 |
| rs141325679 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147946193 | GTCTCCTGCCTCTAT[C/T]AATACACAGTATGAG | 79658 |
| rs141357801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148035702 | GAAGCTCTACCATGC[A/G]GCAGTTATAACCTGC | 79658 |
| rs141360130 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147749228 | TGCCTGGATACAAGG[A/G]CAAGGTTGTTGGCAC | 79658 |
| rs141374315 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147874667 | ATTCTTCTCAGGTAG[C/T]TATATTAAAACCTAA | 79658 |
| rs141383364 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147819687 | CCTCAGCCTCCTGAG[C/T]AGCTGGGACTACAGG | 79658 |
| rs141392121 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147917883 | CTTTATTCAAAATGA[A/T]GAATAAGATGATGAA | 79658 |
| rs141426299 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148032103 | CTCCCACTCCTCTCC[C/G]CTTCTTTCTTTATTA | 79658 |
| rs141427839 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147752188 | ACGCCTGGCCAAGCC[C/T]TTAGTATTATAGAAG | 79658 |
| rs141447719 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147734059 | GGAGGAGTTGGGAGC[A/G]GGGGTGCAGAGTGAA | 79658 |
| rs141453243 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147995215 | CCTCTAGGTCAGTGA[C/T]AACCAGTTTTTATGT | 79658 |
| rs141486400 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147915151 | TAGTGTGTAGGATAT[C/T]GGCGGAGTAGGAGCT | 79658 |
| rs141494700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148017423 | GTAAAACTATGTTTA[C/T]CAGGTATAGACAGTA | 79658 |
| rs141499539 | in-del | -/GT/GTGT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147765323 | GGTGTGTGTGCTGTG[-/GT/GTGT]GTGTGTGTGTGTGTG | 79658 |
| rs141500205 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147827480 | AAGCTTGTGGCTGTT[A/G]GGAAAGGGTTTATGG | 79658 |
| rs141507521 | in-del | -/AG | 0.0379877 | 0.132479 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147855191 | TTAAGTCTGAGAAAC[-/AG]ATGCTCAGAGAATGT | 79658 |
| rs141509768 | snp | A/G | 0.0501905 | 0.150254 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147791546 | TGTGCGCGCGCGTGC[A/G]TGCGCGCGTGTATAT | 79658 |
| rs141579584 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147752806 | TGCCGGGATTACAGG[C/T]GTGAGCTGCCGCACC | 79658 |
| rs141593137 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147910876 | AACTCTTGTAGCCTG[A/G]CACTGGTGATGGACA | 79658 |
| rs141594377 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147986581 | GTGCTGTCTCCAGGG[C/T]GACGTACACCCCACA | 79658 |
| rs141604198 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147972208 | AGACATGAGATTGGC[A/G]TAAGAAAATATTTAT | 79658 |
| rs141610829 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147886371 | CTCAGCCATTCTCTC[A/C/T]GGTGTTCATTCCTTA | 79658 |
| rs141611430 | snp | A/T | 0.0256215 | 0.110247 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148050080 | TCATGTTGGTGAGGC[A/T]GGTTTCAAACTCCTG | 79658 |
| rs141612150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148046533 | GAAAGGAAGAGGTTG[A/G]ACCCCACAGGGCTGG | 79658 |
| rs141641771 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147929959 | CACATGTGTGTATAT[A/G]TATGCACATGTGCCT | 79658 |
| rs141653720 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147745828 | GTTTCGCTGTTGTTG[C/T]GTAGGCTGGGTGCAG | 79658 |
| rs141674118 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148006163 | GCCAGCTGCCGTGTT[A/G]AAAGTTCAGCCACCC | 79658 |
| rs141680892 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148048930 | AAAGGGGGTTGGGGG[C/G]AGTAGTTGAAGCAAG | 79658 |
| rs141693276 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148004205 | AAAAATAAAAAATTG[A/T]CTTAAGCTTTGAAGG | 79658 |
| rs141712733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148045814 | TCCTTGCTGTTGCTG[A/G]TGTTCTTGCTTGCTT | 79658 |
| rs141727841 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889749 | AGCATTTTGAAGTAG[A/G]TGATATTTAATAAAC | 79658 |
| rs141734776 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147938918 | ATAAAAAAGTAGAGA[G/T]ATTGGTATAATGAAT | 79658 |
| rs141740314 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147964015 | CAAATAAGATCGTGT[A/G]TTAAGCACGCCTTTT | 79658 |
| rs141745912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147924248 | CTTCCTCTGAGACGG[C/T]GAACCCCGAGTCCTT | 79658 |
| rs141746220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148000583 | CACCTTCTCTGCAGC[A/G]CCTGTTGTTTCCTGA | 79658 |
| rs141751177 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147934520 | GATTTTGGGAGTTGT[A/G]ACTAAGATTGTGGAC | 79658 |
| rs141751269 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147887734 | GGGTGTGGTGGCGGG[C/T]GCTTGTAGTCCCAGC | 79658 |
| rs141755204 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147801581 | ACCGTCTGTTTTTTA[A/C]TATAAAACATTTGAA | 79658 |
| rs141756739 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147809534 | TTGTTGATGAAGAAA[C/T]TAAAGCTCAGAAGCA | 79658 |
| rs141759740 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147742018 | GTGATTTCTCCTGAC[G/T]TGTTGACTTGTTTAC | 79658 |
| rs141772166 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147797929 | CCATGCCATCTCATC[C/T]CATCCCTCTCCTCTT | 79658 |
| rs141780621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147767442 | TTTCCCTGCATGTCT[A/G]GTATCAGAATTTTGA | 79658 |
| rs141794762 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147893059 | TGGAATTGAATGGAA[A/G]TAAATTTTTTTTTTT | 79658 |
| rs141805733 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147843938 | TTCCATTTTTCTACC[A/G]TCCTACCTCTCTACT | 79658 |
| rs141814865 | snp | C/G | 0.0418186 | 0.138422 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147890693 | TTAACTGGGTGTGGT[C/G]GTGGGTGCCTATAAT | 79658 |
| rs141816044 | snp | C/G/T | 4.94393e-05 | 0.00497164 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148023330 | CATCACCCCCAAATG[C/G/T]GCCACCAAGGCAGTC | 79658 |
| rs141818952 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147804453 | TTGTGAATAGTGCTG[C/T]GATGAACATAAATGT | 79658 |
| rs141848903 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147769847 | AATTAAGACATGTGT[A/T]GAGGGAGGAAAAGGG | 79658 |
| rs141852876 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147995800 | CTGCTCACTGCGAGC[C/T]TCGCCTCCTGGGTTC | 79658 |
| rs141861015 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147803869 | TAATTCTATGTTTTG[A/G/T]CTGTTGTGACTACTG | 79658 |
| rs141861210 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147733327 | GTGATGCTACTGGAA[A/C]ATGGGGCGGAATTAG | 79658 |
| rs141868079 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147767900 | CAGGACAGACACATT[A/G]GAGCCCTTTAGAAAG | 79658 |
| rs141883900 | snp | A/G | 0.000115514 | 0.00759894 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147879301 | CAGCAAAGAAGTTCA[A/G]CATGATCCCATTTGA | 79658 |
| rs141899884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148067323 | TTACATCTTCTGTGC[A/G]TAGTTGATCTCTTAG | 79658 |
| rs141910663 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147951574 | GTATGTAAGGAATAT[A/G]TGTACCTTAACATTT | 79658 |
| rs141912202 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148072614 | GCGTCTCAAGCCTGC[C/T]CTTCCTAGACGGCCA | 79658 |
| rs141915634 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148063341 | AATATGGTGGCAGCA[C/T]ACACAGGGGGCTTGA | 79658 |
| rs141933862 | in-del | -/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147927883 | GATCGGGAGACCTCT[-/G]GGGAGAGTGTGGGGC | 79658 |
| rs141934508 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147828526 | ATTGGAGGAGATGGC[C/T]GAAAGAAGGCATGTA | 79658 |
| rs141938662 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147754112 | GAACAGTGCCTTGCT[C/T]ATAGGCACTGAGTCA | 79658 |
| rs141942059 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147768197 | TTCTCAGTGCAATTA[C/T]ACTGTGAGTGGCATC | 79658 |
| rs141969680 | snp | A/G | 4.19542e-05 | 0.00457989 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147946542 | CATTTAAAAATGGAA[A/G]CTTTGTGAGCTAGAC | 79658 |
| rs141973869 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148019830 | TAGCTGTTAAGATTT[A/G]AAAGCCAGGATAGTG | 79658 |
| rs141976741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147989004 | ATCGGGGACCTGCCC[C/T]GATAATCACGTAGGT | 79658 |
| rs141989153 | in-del | -/ACTTAA | 0.0356815 | 0.128715 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147778889 | GTTTATGGTGGAAGG[-/ACTTAA]ACTTTAATTTGAAGG | 79658 |
| rs141989919 | in-del | -/T | 0.0592355 | 0.161582 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147771795 | GCAACTAAATTAGTA[-/T]TTTTTTTCTTTTCTT | 79658 |
| rs141994212 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147771297 | AGCAGTGAAAATGAC[A/T]TGTGCTCAAGTGGGT | 79658 |
| rs142022559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147946871 | AAGGTAACTAGTAGA[C/T]GCACATCAGTAATTA | 79658 |
| rs142031371 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148020450 | GATGCTCTCCCTCCC[C/G]CTGCCCCGCTGACAG | 79658 |
| rs142071561 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147891699 | AAGGGTCTTAAATCA[C/T]TATAAACTATCACTA | 79658 |
| rs142098787 | snp | G/T | 0.0554779 | 0.157039 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147769001 | CCTCGGCCTCCCAAA[G/T]TGCTGGGATTACAGG | 79658 |
| rs142101308 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147997083 | CTGTAGTGCACGGAA[C/G]AATAACACAGATATC | 79658 |
| rs142102685 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148023819 | TCGCTCTGGGGTTTA[C/T]GGCTTGTGTGCCTTA | 79658 |
| rs142116745 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147846746 | AGTCCTAGTTCTTTA[C/T]ATAATGTAGTCTGAT | 79658 |
| rs142128473 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147878220 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 79658 |
| rs142134563 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147953428 | GCAAGATTTTTAACC[A/G]CAAATTCAATAGGAC | 79658 |
| rs142138271 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147946987 | ACTATGAAACAACTC[A/G]TCGAGGCTGATGATT | 79658 |
| rs142142305 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147872332 | ACCAGGCTTCTTACT[C/G]TCTGGGAAAAAATTC | 79658 |
| rs142149435 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147909356 | TTGTTTCAGAACTCA[A/G]TTGCCAGCTCACTGC | 79658 |
| rs142154841 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147821306 | GAAATAGATGAGTTT[A/C]CATGGGAGGAGCTGC | 79658 |
| rs142160326 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147830400 | ATGCTCTCAAATCTC[A/C]TCCATAAGTTTTTGG | 79658 |
| rs142162850 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147950979 | CCCAACAGATCCCAA[C/T]GAGTGGCAAAGAGAG | 79658 |
| rs142168908 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147985431 | ACATGCAAACCAGTT[C/T]CAGGCCACCAAGCTG | 79658 |
| rs142210087 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147862189 | TGGGGTTACCAGGGG[C/T]GCTGGCATGTCAGAA | 79658 |
| rs142211301 | in-del | -/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148040815 | TATTAAAAAAGATTT[-/G]GGGGGGGGTTATTTG | 79658 |
| rs142215827 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147782489 | AGTCGTCTTAACATC[A/G]GCAAGAACTAAAGCT | 79658 |
| rs142219925 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147827840 | GAGATGGGGTCTCGC[C/T]CTGTCACCAGGCCTG | 79658 |
| rs142229091 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147789086 | TGTGACCTCCCCTCT[A/T]AGCGTCTCCCACTGT | 79658 |
| rs142230648 | in-del | -/TA | 0.0854556 | 0.188216 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147855416 | AGAAAAGAGAGTAAC[-/TA]TGTAATATCAATACA | 79658 |
| rs142233308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147745131 | CCATGCCACAGAGAG[A/G]TCAAGTAGCTTGAGT | 79658 |
| rs142242257 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147948361 | AAAATTAATATCCAG[A/C]ATTCAGTCCATGTTC | 79658 |
| rs142244977 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148023178 | AATGAACTCCAAATC[A/C]AATGTTGTGGTGCTG | 79658 |
| rs142251114 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147907969 | TGCTTCAGCCTCCCA[A/C]GTAGCTGGGATTACA | 79658 |
| rs142259282 | snp | C/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148009478 | TCTTGAGGTAAAAAA[C/T]GTTAAGATCCTCTGA | 79658 |
| rs142262778 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147795127 | TCACTGTGTCACCTA[C/T]GCTGGAGTGTAGTTA | 79658 |
| rs142271839 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147824445 | TACTGGACATATTAG[C/G]TAAGTTGGTTTACCT | 79658 |
| rs142277598 | snp | A/C | 0.0189856 | 0.0955633 | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147781450 | CAAGTCATATATACA[A/C]ATTTAAAAATACGGG | 79658 |
| rs142298763 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147748240 | CCTGGGTCACTTGCC[C/T]GGCATAGACCAGTCA | 79658 |
| rs142322537 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147972322 | TCCATACACTTAAAA[-/T]ATATATATATAAAAC | 79658 |
| rs142337703 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147785811 | TTTTAATATAATAGA[C/T]TTCTAAATAATTATA | 79658 |
| rs142355382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148043849 | TTTTTAAGTTTTATT[A/G]TTTTCATAGTAGTTA | 79658 |
| rs142367610 | in-del | -/ATATATATATATATATATATATAT | 0.0865458 | 0.189163 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147766800 | CATACATATATTCAC[-/ATATATATATATATATATATATAT]ATATATATATATATA | 79658 |
| rs142383275 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147978470 | CTTAGTGGGAGGTGA[C/T]TGGATAATGGGGGTG | 79658 |
| rs142399000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147923085 | ATATTGTGTGTCTCA[A/G]CAATTTCTAAAGTTA | 79658 |
| rs142400532 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147901884 | TATTATTTTTCCTCC[A/C]CATATGAGCATCAGT | 79658 |
| rs142400800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147968823 | AGATTGCATCATATG[C/T]CAGACATGTAGTAGG | 79658 |
| rs142404080 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147790265 | TCTTACAATAATTCC[A/C]TAAGGTGGGCTTCAC | 79658 |
| rs142405803 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147853651 | GCTTAATGAAGAATA[C/T]ATTTTGTGTTACAAA | 79658 |
| rs142437660 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148004865 | GAACTTTGAGATCAT[C/T]GATAGCTTTCTTATT | 79658 |
| rs142445556 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147963477 | TGACGCCTGTGAAAA[C/T]TAGCAAAATCTTCAA | 79658 |
| rs142448405 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148042798 | AAGCTCAGTAAATGC[C/T]AGTTGGGTGAATAAA | 79658 |
| rs142468491 | snp | A/G | 6.59185e-05 | 0.00574064 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148023287 | ACGCCGCCCGATACT[A/G]CATTCCCTGAGCCCA | 79658 |
| rs142472760 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148048221 | TGGGCATTCTGGGGA[A/C]TTTAAATGGACTGGA | 79658 |
| rs142479942 | snp | A/G | 0.000924474 | 0.0214798 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148046898 | TCCTCCTAGGTGACA[A/G]TCCTTACCCTTCCAA | 79658 |
| rs142501616 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148007779 | ATACAAGGTTTACAA[C/G]GTTATTCCTCTTCCA | 79658 |
| rs142511271 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147848311 | GGGCTACGAATTGAG[G/T]CTCAGACCCTGTGAA | 79658 |
| rs142512149 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147965962 | CTATAAAAAATGTTA[C/T]GCAAAGGCTTTTTGA | 79658 |
| rs142531496 | snp | A/C | 1.654e-05 | 0.00287571 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147875087 | AAAATCAGACAGAAT[A/C]CCAAGGACCACAAAC | 79658 |
| rs142538477 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147735746 | GAGAGAAGAGCCAGT[C/T]ATTTTAGTGGTGGAT | 79658 |
| rs142544558 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147802384 | TGATTTTGCAAACTT[C/G]TTTTCTCTAAAGCAT | 79658 |
| rs142555533 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148034110 | GGAACAACTGAGTTA[A/G]TGGATGTAAACCAGC | 79658 |
| rs142566097 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147733719 | AATATGCATTTAATG[A/C]ATAAGTTGAAGTACA | 79658 |
| rs142572152 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147840450 | CTTTTTAGCATTCTG[A/G]TTACATTCCTGCTTT | 79658 |
| rs142574077 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147895098 | TGAACTTGATTTTCC[A/G]TTTATTTAGACTTTC | 79658 |
| rs142578066 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147970193 | TTGCTGACAAGGGTG[A/C]TTGTGCAGGAAAACT | 79658 |
| rs142586699 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147916405 | CTATTCAGTATGTGT[A/C]TGACTTATGAAATGT | 79658 |
| rs142587956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147800759 | GCGCTTAGTAGGGAG[A/G]AGCAGAGAGACATAG | 79658 |
| rs142588670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147993674 | TCAAAGCCAGGTTAA[C/T]ACCATTTCTGCAATT | 79658 |
| rs142593681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147874877 | AGGAGGCACACTGGA[A/G]AGAATGGGGGTATTT | 79658 |
| rs142600102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147802977 | AAATTCTATTTATCA[A/G]CCTCTCTCCACTTTT | 79658 |
| rs142607089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147768680 | ATAAATTTGGTGACA[A/G]CTTTGTTTTTGAGTT | 79658 |
| rs142616540 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147793475 | GGAGCCTTAACAGTT[A/T]TATCTAGAAAAAGAA | 79658 |
| rs142639443 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147846177 | TTTGAGTGTTCCCTA[C/T]GTTAGAGTATGAAGG | 79658 |
| rs142668525 | in-del | -/CG | 0.498323 | 0.0289051 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147741800 | ACACACGCACACACA[-/CG]CACACACACACACAC | 79658 |
| rs142673668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147982026 | TTCAATTTGCCACCC[C/T]ATGTCTTTTATTTTT | 79658 |
| rs142673999 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148062280 | GGAAACAATCTGAGA[A/G]CATGCTGAGGAGTGC | 79658 |
| rs142676614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147734244 | CTGGTAGAAAGCTAT[C/T]TCTGTGACAGCATAT | 79658 |
| rs142696846 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148070079 | TCATGTGTCTGACAC[A/G]GTGCTAGGTGCTGGG | 79658 |
| rs142703079 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147860088 | AGAGTTGCAGAGAAT[C/G]ATACTGAACAAAGGC | 79658 |
| rs142708858 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147939185 | GCATACCAAATTAGG[C/T]TTGACAATACATTTT | 79658 |
| rs142731783 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147989275 | AAGTGGAGGCAGGGC[A/G]AGATCACAGGACCAC | 79658 |
| rs142738227 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147863436 | CAGAATTTCCTTCCT[A/G]TCTAAGGCTGAATAA | 79658 |
| rs142744033 | in-del | -/TAAT | 0.0146672 | 0.084371 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147768514 | ATTAAAAAAAAAAAG[-/TAAT]TAAAGGTTGAGATTT | 79658 |
| rs142757540 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147944867 | GCCTCCTCCCTTTGG[A/G]TAGGTACCATCACTG | 79658 |
| rs142761775 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147974705 | CCTAGTACTAGCCTG[C/T]ATTAGTCTGTTTTCA | 79658 |
| rs142763976 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148052663 | CTCTAGGAGAGCCTA[C/G]TGCCTTCTTGTGGAA | 79658 |
| rs142776301 | snp | C/T | 0.232943 | 0.249417 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147757442 | CTCAGGCAATCTGCC[C/T]GCCTCGGCCTTCCAA | 79658 |
| rs142787030 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147867841 | TGCACTCCAGCCTGG[A/G]CGACAGAGTGAGACT | 79658 |
| rs142797365 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147815212 | ACACATCTCTGGGTT[C/T]CACTACTTCCTGGTT | 79658 |
| rs142801269 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147819029 | TAGCACAGGTACAAA[A/G]CATGCTCTTTACATA | 79658 |
| rs142807246 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147747524 | GACACCCTGACCGCC[A/G]TGGAGGTGGCCACAC | 79658 |
| rs142836668 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148021780 | GTTTGCTATTGGCCA[C/G]AGTGGTCTATTGGAA | 79658 |
| rs142871757 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148038792 | TTGTGCTCACCCTCC[A/G]CTGGTGAAAGAGTTC | 79658 |
| rs142876032 | snp | C/G/T | 0.000355758 | 0.0133329 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147875024 | AATCCATTTCAGACA[C/G/T]GGAATCGATTTGAAG | 79658 |
| rs142892240 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148025786 | GTCAAAACGACTTGA[A/T]GGTTTCAAAAAGTTT | 79658 |
| rs142901198 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148013023 | CCTTTGTAACATGAA[C/T]AAATTGTAATTTGGG | 79658 |
| rs142902353 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147940220 | TAGCCTGTCCAGAAT[A/T]GTGACAGTACATTTG | 79658 |
| rs142907822 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147987570 | TGAGGCTTGGTGCCT[G/T]TCTTCTCTGGGTCTG | 79658 |
| rs142908675 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148047948 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 79658 |
| rs142915452 | in-del | -/AGAG | 0.0919752 | 0.193722 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147921559 | ATTTGGGATAATGAC[-/AGAG]AGCATGTGGATGTAA | 79658 |
| rs142924897 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147811596 | GGCTTTTTTTAAAAA[A/C]AAAAAACAAAAAACA | 79658 |
| rs142931536 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147919043 | TCCGAAGGTGGCTCA[C/G]TTCTCCTTACCTCTT | 79658 |
| rs142932760 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147927756 | TAGGGGAGCTTGATC[C/G]TAAGGGAAGGCGCAG | 79658 |
| rs142937455 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147996276 | AGCAATAAACAGAAA[A/G]GCAGTCGAAAACAAA | 79658 |
| rs142950905 | snp | C/T | 0.0898077 | 0.191933 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148000109 | GGCCCCAGTGTGTGA[C/T]GTTCCCCTTCCTGTG | 79658 |
| rs142956222 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147865818 | TTAGAGAAAAACTCA[A/G]CCTCCTCAAAGCTTT | 79658 |
| rs142956700 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147773458 | GGCTCTGTGTTTTAG[C/G]ATTACAGCTGCCCAG | 79658 |
| rs142958260 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147914999 | GTGAAGTATGTATAA[A/C]TGGAATATTTAATTC | 79658 |
| rs142972469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147991074 | ACCTTGGTGACAAAA[C/T]AACCTTTACACCAAA | 79658 |
| rs142999495 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147786426 | GCTTAGTTCTTAGCA[A/G]TGGCAGGGAGAAGTG | 79658 |
| rs143008821 | snp | A/C | 0.000703954 | 0.0187478 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147946613 | TTGTTTGCTTGCTCA[A/C]TAGATGTAAAAACAT | 79658 |
| rs143013564 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147790927 | GGCTCCTGTGACCCC[G/T]CCTCATCCTGTGTCC | 79658 |
| rs143025336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147871626 | TAGATTATTGTGAGG[A/G]TTAAAGAACCATGTA | 79658 |
| rs143027125 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147762080 | TGGCACAATCTCAGC[C/T]CATCGCAACCTCTGC | 79658 |
| rs143035312 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147820388 | CCTCCTGAGTTCAAG[C/T]GATTCTCCTGCCTCA | 79658 |
| rs143047224 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148054607 | AGATGTTGACCTGAA[A/G]TTGTGTTGTTTTTAG | 79658 |
| rs143076680 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147750109 | TGTAAAGACCTTTGT[A/G]TTTTTTGACCTTAAA | 79658 |
| rs143085365 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148065744 | AAGACTCTGAACTCC[C/T]TCCTGCAGTATGGTT | 79658 |
| rs143111127 | in-del | -/G | 0.0501905 | 0.150254 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147884704 | GATTGAGAGTCATGT[-/G]CCAGGTAGAGTGAGT | 79658 |
| rs143115755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147942343 | CTCTGTAGTTCTTGA[A/G]AGCTAATTATTTACT | 79658 |
| rs143117799 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148015285 | GAAGGGGTCAAAGCC[A/G]GCAAGATAGGAAGTA | 79658 |
| rs143120025 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147756015 | TGTCACATAATAAGT[C/T]AATAGTAGGTGGTTG | 79658 |
| rs143124412 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147962818 | ACAGGTGCACACCAC[C/T]ACACTGGCTAATTTT | 79658 |
| rs143125525 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147763907 | TTACAGGCGTACGCC[A/G]CCATGCCTGGCTAAT | 79658 |
| rs143128816 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148041051 | AAAGTAGGTTTCAGC[A/G]TCCCCCAGCTAGCCA | 79658 |
| rs143144531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147814974 | TAATTACCATAGCAC[C/T]CATTAAACCAGGCTT | 79658 |
| rs143169819 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147839122 | TCTATCTATCTATCT[A/G]TCTATCTATCTATCT | 79658 |
| rs143176775 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147899262 | TTCTTTGTCTGTGAT[G/T]GTTTCCTCTTTGTCT | 79658 |
| rs143182616 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147920479 | CAAAGTCCCAAAGAA[A/G]ATAGCAGAACGTTCT | 79658 |
| rs143187915 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147836477 | GGATATATACTTTAA[A/C]ATCATAGTTTCTAGC | 79658 |
| rs143204656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147775773 | GCACAGAATTATGGT[A/G]TAAAACAGCATGTAT | 79658 |
| rs143245861 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147893928 | ACTGTTGATGGTGAT[A/G]TATTGAAAGACACAT | 79658 |
| rs143282710 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147969263 | TGAAAGCTGATTGGG[A/G]ATTTTCTTTACCATT | 79658 |
| rs143291838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147955059 | ACAAAGCTACTTTCC[A/G]TGATTAGATATGAAA | 79658 |
| rs143292020 | snp | A/C | 0.00110313 | 0.0234595 | synonymous-codon, intron-variant, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148063190 | CCAGTGGCTTAACCC[A/C]CAGTCTCCAACCACA | 79658 |
| rs143298069 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147870873 | GTATTTAAGAATATG[A/G]GCAAAATATTTTTGT | 79658 |
| rs143305866 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147845641 | CAGTTCATTCTGGGC[C/T]GACTTCTTTCTTGAG | 79658 |
| rs143308296 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147770758 | AGCCCATCTGAGCTT[C/T]GGTGTTTGTTTTTTT | 79658 |
| rs143326383 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147915020 | TATTTAATTCACTCT[C/T]ATATATTCTGTATTC | 79658 |
| rs143340981 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147733760 | AAGAATTTAGTGAGC[A/C]ATCCCTGTAATTTTG | 79658 |
| rs143344202 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147939734 | AGGAATGCTGCTAAT[A/G]TTAGTTAGCAAAGAT | 79658 |
| rs143357879 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148012401 | TGCTTTGTCGTCATA[C/T]ATAAGACTTCTTAAA | 79658 |
| rs143368194 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148016325 | CCTGGGTAACAAAAC[A/G]GACCCTGTCTCTACA | 79658 |
| rs143371632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147799328 | GCCTCTCTTTGTTTA[C/T]TCTGATCATAAATTT | 79658 |
| rs143385871 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147760133 | CCCATGGTCTTGCAT[C/T]TGTAACCTTGCTGCT | 79658 |
| rs143394176 | snp | A/G | 0.000233294 | 0.0107978 | missense, utr-variant-5-prime, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147732419 | TTCATCAAAGAGCTC[A/G]TTAAGGACGGGAAGA | 79658 |
| rs143398803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148024249 | TTCCTCTTATTGAGA[A/G]CATTTGCTGAATTTG | 79658 |
| rs143408317 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147943258 | GTTAATTCTAAATCT[C/G]ATTTGCAAGAAGGGC | 79658 |
| rs143420076 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147899801 | TTACATTTCTATAAC[C/T]TTAAAAACTTTTTTT | 79658 |
| rs143423153 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147977307 | GGCGTATGTGTAGGT[C/T]GGCTCCAGGGAAGGC | 79658 |
| rs143431621 | snp | C/T | 1.6477e-05 | 0.00287024 | missense, intron-variant, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148063246 | CTCTTTCACCCGGGT[C/T]GTCCCCTTTCCCCTT | 79658 |
| rs143455450 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147785434 | AAGCTGTATTGTGCC[C/T]GTCAGATCAATAGTG | 79658 |
| rs143475651 | in-del | -/AG | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147773709 | TACCAAAAGCCTTAA[-/AG]AGTGGAATGATAGGG | 79658 |
| rs143486090 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147946640 | ACATGCAATGAGGTG[A/G]ACCTGGAGAATTCTG | 79658 |
| rs143492973 | snp | C/G | 0.0452528 | 0.143452 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147776265 | TGCTCTGTCGCCCAG[C/G]CTGGAGTGCAGTGGT | 79658 |
| rs143496041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148059879 | AGTTCCTACAAGGCA[A/G]TGCAGCTTGGGCCAG | 79658 |
| rs143498441 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148019772 | TCCACCTAAAAAAAA[A/C]AAAACAAAACAAAAA | 79658 |
| rs143531321 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147980631 | CTCTTTTTTGTAAGC[C/G]TGGTAGAATTTGGCT | 79658 |
| rs143532723 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147979624 | GTGGATTGCTTTGGG[C/T]GGTATGGAGATTTTA | 79658 |
| rs143542854 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147984858 | ATCTGTGGAGTGCAC[A/G]GTGGTCTGAGCGCCC | 79658 |
| rs143552684 | snp | A/G | 0.000428449 | 0.0146301 | synonymous-codon, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147866732 | GTCATTTTTTCAGGG[A/G]ATGTTTACCTTCTAT | 79658 |
| rs143554569 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147752562 | TTTTTTTTTGGTGAC[A/G]GGGTCTCATTTGTTG | 79658 |
| rs143557496 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147787153 | GATCAGGGTTGTCAC[A/G]TAATCGGGTGCTGGA | 79658 |
| rs143559022 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148064235 | AATTGGAAACCCATC[A/T]TTTACTTGAAAATCA | 79658 |
| rs143582736 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147797400 | TTCTCATGGTCCAAC[A/G]TACCCTCCCCACTTT | 79658 |
| rs143600360 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148045595 | AATACAAAATTAGCC[G/T]GGCGTGGTGGTGCAT | 79658 |
| rs143611887 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147780010 | TTACATGGGATTGCA[G/T]TATCTTTAATTTTTC | 79658 |
| rs143613010 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147860826 | AAATTGAAATTGTGT[A/G]TTTGTTAAAAACTAG | 79658 |
| rs143654538 | in-del | -/TAAG | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147955218 | GTTTTACACATTAAT[-/TAAG]AAATGCATAACAAAT | 79658 |
| rs143665456 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147744555 | AAAGCAGGACTGGAG[A/G]TTGGGGGGTCAGTCA | 79658 |
| rs143668581 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147850205 | AGCACTCTGTAAAAA[C/T]GGACCAATCAGCACT | 79658 |
| rs143690540 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147738051 | GGGGACTAGGGTACA[C/T]TGTAGACTTTTGGAT | 79658 |
| rs143701070 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147933249 | TAGGGACAAGGTTTT[A/G]CTATGTTGCCCAGGA | 79658 |
| rs143709049 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148036869 | TAGATTACAACTTCT[A/G]GGTAGATGAGGTCCT | 79658 |
| rs143720487 | in-del | -/TTGA | 0.413416 | 0.189196 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147898187 | AGGCTGCCTTAGGCT[-/TTGA]GCATTTCTTGTAATG | 79658 |
| rs143728153 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147944342 | GTCAATTGCCATTGT[C/T]GTAGTTTATTGCATA | 79658 |
| rs143729061 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147803449 | CATTTATCATGTGCT[C/T]TGGGAACATTTCATA | 79658 |
| rs143729542 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147812583 | AGCTGCCCATAAAGC[C/G/T]TTTTCCCCACCTCTG | 79658 |
| rs143731526 | snp | C/T | 0.001038 | 0.0227579 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147866791 | TCAATCACTACAAAA[C/T]GGAACTACAGATCAA | 79658 |
| rs143732969 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147918604 | ATTGTCTTTCTGTTG[G/T]CCATCCCTGGTCTGG | 79658 |
| rs143739192 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147876369 | AGGCCGAGGTGGGCA[A/G]ATCACGAGGTCAGGA | 79658 |
| rs143765476 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147956934 | GGTTCCTAAGAGGTA[G/T]GAGCTTATATCTTAA | 79658 |
| rs143781026 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148032813 | TGGTGTAAGTCCAGG[A/T]GTCCAAATCTGAAGA | 79658 |
| rs143792959 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147817289 | GGCTTGTAACTTAAG[C/G]GGTTATCCTGCACTG | 79658 |
| rs143793976 | snp | A/T | 0.0279526 | 0.114869 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148037674 | ACCCCTTCTCTATTG[A/T]AAATACAAAAATTAG | 79658 |
| rs143819625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147990554 | TCCAAATGCCCATGA[A/G]TGGTAGACCAGATAA | 79658 |
| rs143823475 | snp | C/T | 0.0023933 | 0.0345097 | downstream-variant-500B | ARHGAP10 | GRCh38.p7 | 4:148072806 | CCTAATGTGGGGAAG[C/T]GGTCGTGGAAGTCAT | 79658 |
| rs143829292 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147960010 | ATCCTCAGTAGTTGT[C/G]CTTTTACTCCTTTGG | 79658 |
| rs143835139 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147885623 | TGGGTACAGAGCTTG[A/G]CGGCTATGGCAGCAT | 79658 |
| rs143835915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147800161 | ATTTCCCTAGGCTGG[A/G]CTACTAGGTGTCTCC | 79658 |
| rs143838623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147918810 | TGAGAATCTAGTTCT[A/G]TCTGTAGCTCCTAGA | 79658 |
| rs143843691 | in-del | -/AG | 0.00159681 | 0.0282109 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148024548 | CTCCTGTAATGACAC[-/AG]GGGGACTAAAATGTG | 79658 |
| rs143873956 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147749889 | CTTGAATGGCTATGC[A/G]AATTAACCTGTTGAT | 79658 |
| rs143897623 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147794882 | GTAACCAGTTCCCCT[A/T]CTGATAGACATCTAG | 79658 |
| rs143897889 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147839396 | ACACGTGGAATCCAG[G/T]CTTAAAATAATGAGT | 79658 |
| rs143911557 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148039947 | AATCTCTGAGTTTTC[G/T]TATTCATTGAGTTTG | 79658 |
| rs143941801 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147934889 | AGGAATCAATTATGA[A/G]TTATGTTTAGAAGAA | 79658 |
| rs143947806 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147998962 | GAGGGAAACGAGGTG[G/T]TATCTAAAACCTGGA | 79658 |
| rs143950195 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148007889 | GCTTTGAATGTTCCC[A/G]GTCACAGTCTTCGGA | 79658 |
| rs143952354 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147919914 | GCTCTCATACCCTGT[C/T]AGCCTGACTTAATTG | 79658 |
| rs143959489 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147954071 | AACAAACTCTGTGTG[A/T]CTTAAACCCTTTTTA | 79658 |
| rs143966872 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147838004 | GATGTCTCCCTTCAT[-/C]ATTTACTTGATTAAA | 79658 |
| rs143974654 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147797070 | TGTGTTTGAAGCATC[C/T]GGCCTGGAGCATGGC | 79658 |
| rs143977755 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147891181 | AACTTGTGAATGAGT[A/G]TTCATAGAAGCATTA | 79658 |
| rs143984189 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147804934 | GGTTGTCTGTTTACT[C/T]TGTTGATAGTTTCTT | 79658 |
| rs143993253 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147768711 | TGTTTAAACATTTAA[A/G]TGCTTAAAAATGGGG | 79658 |
| rs144000869 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147883376 | CTAAATTTCAAGCCA[A/G]TAAGAACTCTTCCAA | 79658 |
| rs144024723 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147760949 | GAAATTAATAGCTCT[C/T]AACTGAGAACTGTAA | 79658 |
| rs144031731 | snp | C/G/T | 0.00358938 | 0.0422398 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147958358 | TAAACCAAAACACTT[C/G/T]TGTTGCTATGTTCAG | 79658 |
| rs144047341 | in-del | -/A | 0.0130921 | 0.0798413 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147985512 | TCCTCTTACTTTTGG[-/A]CCTGTGATGGGGGAG | 79658 |
| rs144063515 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147833900 | TGTGGCAGCCATGGG[C/T]ACCTCTCAGATAGAG | 79658 |
| rs144063558 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147888444 | GAGTGGGGGTAGTTA[C/T]ATTCCTCTAACATGT | 79658 |
| rs144067154 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147962100 | CTGCTAAATACCAGC[C/T]ATTTGAATGTCACTT | 79658 |
| rs144095878 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147838626 | GCAGCCTCAACCTCT[C/T]GGCCTCAACTAGCCT | 79658 |
| rs144122508 | snp | A/C/G | 0.000100255 | 0.00707951 | synonymous-codon, missense, utr-variant-5-prime, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147847204 | AAAATTCAGAAAAGA[A/C/G]CAACTTGGAGCTGTA | 79658 |
| rs144123480 | in-del | -/GTTA | 0.0217236 | 0.101931 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147855363 | TTCAGTTTATTTTCT[-/GTTA]GTTGTTAAAATAGTG | 79658 |
| rs144126450 | snp | C/G | 0.0126979 | 0.078662 | upstream-variant-2KB | ARHGAP10 | GRCh38.p7 | 4:147731033 | TGCCACCGCACCCGG[C/G]TACTTTTTGTATTTT | 79658 |
| rs144141624 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147977295 | GGCGAGTGTGGTGGC[A/C/G]TATGTGTAGGTCGGC | 79658 |
| rs144144539 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147960051 | ATTTTGCAGAGTCTC[C/T]GCTTTAAGTCTATTT | 79658 |
| rs144146053 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148064770 | ATTCAGGTCATCTCT[C/T]TCCTGACGGGAAGAA | 79658 |
| rs144151785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148014362 | CAAATGTTTGCAGGT[A/G]CAAATTGATAAAACT | 79658 |
| rs144180385 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147736538 | AAATAAAATGGTGTG[A/G]AAGTGTTTTGAAACA | 79658 |
| rs144184860 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148018341 | ATCCAGGCAGTAGTT[C/T]CAGAATTGGCAAATC | 79658 |
| rs144185537 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147887590 | TTCCTGGCCAGGTGC[A/G]GTGGCTCATGCCTGT | 79658 |
| rs144197814 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147837955 | TGAACACGTATACTT[G/T]TAGGTATGCATATGT | 79658 |
| rs144200944 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147852875 | AGACATGCGCCAGCA[C/T]GCCAGGCTAATTTTG | 79658 |
| rs144201008 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147802789 | TTACCTTCTCAAAGT[A/T]GTTTCTCATCAATCT | 79658 |
| rs144207083 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147764216 | GTTTGGGGTATTGAT[C/T]GAGCTAATTTTGGTG | 79658 |
| rs144209532 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147902912 | AAGAGAGAGAGAAGT[A/G]GGAGGGGAGGGCGGG | 79658 |
| rs144213810 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147805362 | AGTACCATGCTGTTT[C/T]GGTTACTGTAGCCAT | 79658 |
| rs144220284 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147873623 | TTGAGCCCAGGAGTT[C/T]GAGACCAGCCTGGGC | 79658 |
| rs144239651 | in-del | -/GT | 0.145978 | 0.227331 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147988168 | GAAAACAGATGGAGC[-/GT]GTGTGTCTGGTCAAC | 79658 |
| rs144250110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147948245 | GATAATACTTTAAAG[A/G]TTTTCTGAAACATCA | 79658 |
| rs144258256 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147777634 | TGTCAGACGGTCAGA[A/T]CTCTTAACACTGGAT | 79658 |
| rs144268142 | in-del | -/AAC | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147785106 | AAAAAAAAAGAATAA[-/AAC]CATCTAAGCTAAAGG | 79658 |
| rs144268679 | in-del | -/G | 0.0360663 | 0.129354 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147779474 | GGGGAAGGGTCCTGA[-/G]GGGGGAAAGCAAGCT | 79658 |
| rs144270317 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147979130 | AATTTTTTGCCTAGG[C/T]GACTATCTGGAAGAG | 79658 |
| rs144297934 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148069000 | GGCATAGGGAGGGTG[C/T]GTGGGAAATGACAGA | 79658 |
| rs144299187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148024002 | GCTGTTCAGCTAATC[A/G]TTGCCACGTGGCCCT | 79658 |
| rs144308492 | in-del | -/TTTTGAAACTTAGTGTTAT | 0.227074 | 0.248947 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148038938 | AAAGTGGTGCCTTTG[-/TTTTGAAACTTAGTGTTAT]TTTTGAAACTTAGTG | 79658 |
| rs144309685 | snp | A/C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148028830 | GATGTTAAAGCAAAT[A/C/T]GGGGACTTCTCAACT | 79658 |
| rs144317273 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147832158 | TTTAATTGTCTAATC[C/T]AGAGGAGTGATTCGA | 79658 |
| rs144321012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147906957 | TTGCCACTCTGATTT[A/G]CTTTGCTTGAGGAGG | 79658 |
| rs144322998 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147854934 | ATTCCCAACTTTACC[C/T]ACATGTTGATTTTCA | 79658 |
| rs144349734 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147791537 | GTGTGTGTGTGTGCG[C/T]GCGCGTGCGTGCGCG | 79658 |
| rs144357011 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148016873 | GCTCAAACACATTTA[A/C]TGATTTGTTATAAGG | 79658 |
| rs144357408 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148016106 | CATGTGGCAAGTACC[A/C]AAAAGTTGCAACTGT | 79658 |
| rs144369804 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147913239 | TGTTACAGAATGAAA[C/T]GTGTTAACACAAATG | 79658 |
| rs144376278 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147989808 | TATACATCCTTCTCG[A/G]CTGACAGGATTAAGA | 79658 |
| rs144378672 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147901477 | TTTGCCAAAATATAA[A/G]CAAATGGAATTCTTT | 79658 |
| rs144380491 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147817148 | ATTTATTAACCATAC[C/T]CTTTTTCTTTTCAAG | 79658 |
| rs144388998 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147860528 | GGCAGTTCTCTGAGG[C/T]CTTGCTGCTATACCT | 79658 |
| rs144402547 | in-del | -/CCCCC | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148032342 | TCCCCCCCCCCCCCC[-/CCCCC]ATATTGTAGGCCAAA | 79658 |
| rs144414765 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147777074 | TATGCTGATAGCTGT[C/T]ACAGTCAGTTTTCTT | 79658 |
| rs144437569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147916241 | TTCATATGGTTCGGT[C/T]AAAGCCATTAGCCTT | 79658 |
| rs144437574 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147868886 | CCTGCCATGTGACCC[A/G]GTTCCTAACAGGCCA | 79658 |
| rs144440676 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147744510 | TGTAGAAAGCTTTCT[C/T]GGAGTGCAGTTGTGC | 79658 |
| rs144451277 | in-del | -/CTC | 0.130694 | 0.219696 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147985964 | CTGTTTGCCCACCTT[-/CTC]CCTCTCTGGAGTCTG | 79658 |
| rs144456392 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148011359 | ATTTTGAATAGCTGT[A/G]GGCTGGAATCATCTG | 79658 |
| rs144490603 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147971836 | GGATTTGCAGTAGGA[A/T]GTAGAGGAATGAAAG | 79658 |
| rs144494237 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147993021 | ACTTCTTATGCAGAT[A/G]TTTGTAGAATTACCT | 79658 |
| rs144499573 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147958280 | TCATGGTGCTTAGTA[C/T]GAGAATGACAACTAA | 79658 |
| rs144507431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148035576 | CATTTTGTCTTGCCA[C/T]GTTTCAGAGGGAAAA | 79658 |
| rs144508725 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148033607 | ATATAAATACACATA[C/T]ACACACATACCGCAT | 79658 |
| rs144510983 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147772415 | TTTTTTAAGCCACAG[C/T]TCTACAGACAGATGG | 79658 |
| rs144516407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147847318 | TTTGAAGGAGATGCC[A/G]GAGCAAACCATCTGT | 79658 |
| rs144542753 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147735284 | TGCACTGTGCTAAAT[C/T]CTTGAAGAAACAAAG | 79658 |
| rs144559487 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147958651 | ATTTCACGGTAGATA[C/T]GAATGCCACAGGAGA | 79658 |
| rs144563544 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147916978 | GGGAGCCAGGATACA[C/G]ATTATGTGTTTGAAT | 79658 |
| rs144593811 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147752031 | GCTAGGACTATAGGC[A/G]TGCGCCACCACACCC | 79658 |
| rs144599935 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147835433 | GCTGGAGTGCAGTGG[C/T]AGGATCTTGGCTCAC | 79658 |
| rs144604709 | snp | A/G | 0.00368565 | 0.0427696 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148047021 | ACCTTCTGGCAGATG[A/G]AGGGAGCTTTGGAGA | 79658 |
| rs144606803 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147793714 | GGAGTTAACATAATG[C/T]GGAGCCATGGATCCT | 79658 |
| rs144616792 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147923920 | TAAATTGCCAAGGGC[A/G]ATGAAGAAAATAAAG | 79658 |
| rs144625449 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148026748 | CATATAACATTTAAT[A/C]TCAACATCAAAGCTG | 79658 |
| rs144656636 | snp | A/G | 0.0973687 | 0.197999 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147754980 | CCAGCTACTTGAGAG[A/G]CTGAGGCAGGAGAAT | 79658 |
| rs144657176 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147797720 | CTGGCCAGCCAACAC[A/G]CCCGGCCCCCTCCCC | 79658 |
| rs144675216 | snp | A/T | 0.00318978 | 0.0398085 | upstream-variant-2KB | ARHGAP10 | GRCh38.p7 | 4:147730745 | CTCGTTAATATTACC[A/T]TCATATCATGTAAGT | 79658 |
| rs144713852 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148048254 | GTGTTCCTCAGATTA[C/T]GTGGCTTTTTATAGT | 79658 |
| rs144720198 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147867567 | TTCATTTCTTTCACA[A/G]TTAGAAGTTGAGAGT | 79658 |
| rs144721560 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148051888 | TTTTTATTCTCGTCA[A/G]TGCAATCACTTGTTT | 79658 |
| rs144731909 | snp | C/T | 0.00301132 | 0.0386858 | synonymous-codon, intron-variant, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148063154 | TACCCTTAGCCCAGG[C/T]CAGACCCGATCGTCT | 79658 |
| rs144743920 | in-del | -/T | 0.0785177 | 0.181917 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147874456 | TTTGTGTAGGTGAGA[-/T]TTTTTTTTCCCCCTT | 79658 |
| rs144747245 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147970336 | TCCCTCTTAGTGTTT[C/T]AGGACAAGATGAAAA | 79658 |
| rs144763694 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147794836 | GATTTTAATGTTCTT[A/G]TGGTGTTCTATCATG | 79658 |
| rs144786855 | snp | C/T | 3.29544e-05 | 0.00405908 | synonymous-codon, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148023308 | CCTGAGCCCACCTGC[C/T]TGTCAGCATCACCCC | 79658 |
| rs144798789 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147753954 | ATAGTTTGGGGCTTC[C/G]ATTCATCTGCTACTA | 79658 |
| rs144801501 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147983860 | CCTTTGAAGGTGACA[A/G]AACAGTCTGGCTTTT | 79658 |
| rs144801678 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147861582 | TGGAGGGTGAGCAAG[A/G]TACAGGGGAACTTCA | 79658 |
| rs144804584 | snp | G/T | 0.000235742 | 0.0108543 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148063316 | GTACGTGGTTTGGAG[G/T]GGAATGTGGAATATG | 79658 |
| rs144808169 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148048870 | GCTTCCTATTCATAC[A/G]CATTTTAAAATGTCA | 79658 |
| rs144818835 | snp | C/T | 0.000266458 | 0.0115394 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148047071 | GTAACCGTGCTTCTG[C/T]TGGGTGCTGAAGGGT | 79658 |
| rs144821459 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147830481 | TTGCGGTTTTTGCCA[C/T]TTTTTTTTTAAATGG | 79658 |
| rs144835990 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889431 | CAGCCTCCCAGGTAG[C/G]TGGGATTACAGGCAT | 79658 |
| rs144837599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147940051 | AGAGACAATTGACCC[A/G]CAGAAGTAGATTAGT | 79658 |
| rs144837812 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147935625 | ATAAACTCACTAATA[C/T]GCCTTGGCATATTGG | 79658 |
| rs144853053 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147744140 | CAGTATGGGATGCGA[C/T]GACTGTAGTTAACAG | 79658 |
| rs144861100 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147810859 | GTCACTTCATTAACT[C/T]AACAAATACTAATTG | 79658 |
| rs144866398 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147974825 | CACAATCATGGCGGA[A/C]GGGGAAAGGCATATC | 79658 |
| rs144870889 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148053431 | GGGGAATAAACACTT[G/T]AATCTGGTTGCTGCG | 79658 |
| rs144877361 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147800088 | TGGTGGTTAGATGCC[A/G]CTAGGGCTGCCGTCT | 79658 |
| rs144882528 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148029875 | ATGATGAGATCAATG[A/G]GTTGGAAAAGGCAGC | 79658 |
| rs144893967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147805622 | ATTTTTTAAAAAACT[A/G]GTTCTTAGAAAACCA | 79658 |
| rs144904371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148008758 | TCAGGGTTCTGTGAG[A/G]TGAGAGCTATTTTTC | 79658 |
| rs144906149 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147914165 | TCAAAAAAAGAAATC[C/T]GCTTTATTGAGGTAT | 79658 |
| rs144915073 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147990473 | GTCAGAGTGGGCAAC[A/G]TGGCCACTTGATGAA | 79658 |
| rs144923912 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147934399 | CCCACAGAGAGACTT[G/T]GATGGTGGATGGATG | 79658 |
| rs144939603 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147937445 | ACTGAGGATTAGGAC[A/G]TCAACAGATGAATTT | 79658 |
| rs144943812 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147803937 | ATGCTGATTTTCTTT[G/T]CCTTGGATAAATATT | 79658 |
| rs144945704 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147856201 | ATTTATAAATGTGTA[C/T]ACTTATTTTCTCAAA | 79658 |
| rs144951073 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147892774 | GTTCTCAACTGTGGG[C/T]GATGTTGCTCCTAGG | 79658 |
| rs144976888 | snp | G/T | 0.0209421 | 0.100162 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147795734 | CAGTCTCACTCTGTT[G/T]CCCAGGCTGGAGTGC | 79658 |
| rs144981159 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147877708 | CATTGTCCTGTGAGC[C/T]CTGATGGTGGTACTG | 79658 |
| rs144981612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147738730 | CAAAATAGCTGTTCT[A/G]CACCCTAGACCAGGT | 79658 |
| rs144995912 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147741148 | TTGATGTTCTATGAT[A/G]ATGTACCTTCTACCT | 79658 |
| rs145004922 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147769512 | TCTTTATGTAATAAA[C/T]TCCTTGTTAACTGAC | 79658 |
| rs145010096 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147807477 | AATTAGAAAATTAAA[C/G]AGAATTTTTCTGAAA | 79658 |
| rs145020343 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147985122 | CCAGGAGATCTGCTT[A/G]GGTATGGAGCAGAGA | 79658 |
| rs145038841 | snp | A/G | 0.0107347 | 0.0725747 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148064778 | CATCTCTCTCCTGAC[A/G]GGAAGAAGCTAGTGT | 79658 |
| rs145059691 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148031783 | GGACTATGGTTTTCA[A/T]TGTGGGACATAAAAC | 79658 |
| rs145071301 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147772522 | TTCTAGCTCAGACTT[A/G]TACCACAGGCCTGTG | 79658 |
| rs145085629 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147941941 | TTCATATTGAACACT[G/T]ATTGAGTGTTCAAAT | 79658 |
| rs145089840 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147862158 | TCCAAAGTCCAGAGG[A/G/T]GGCCGAGCTGGAGGT | 79658 |
| rs145092637 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147991359 | ATCATAAGAGAAAAA[C/G]ACACAGGTGGCATCT | 79658 |
| rs145152694 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147995225 | AGTGATAACCAGTTT[C/T]TATGTTTCACATCCT | 79658 |
| rs145187046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147950210 | CTGTTCTTTTCCCCT[A/G]TGTTATTTTTAGCGA | 79658 |
| rs145187817 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147875702 | TACTAAAATCATCAG[C/G]AAGATTGCAGATGGT | 79658 |
| rs145190850 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147997131 | TTCAAGAAGTTGTCA[A/C/T]CCCTGGTGTAGTGGT | 79658 |
| rs145197104 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147827420 | AAACAATATACAAAG[C/T]GCGCCAGCAAAGATA | 79658 |
| rs145203797 | in-del | -/G | 0.0414363 | 0.137845 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147994392 | AATCCTTGCACAGCT[-/G]GGTGTGGTGTTTGTC | 79658 |
| rs145204086 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147751932 | TGCTCTGCCATCAGG[A/T]TGGAGTGCAGTGGCA | 79658 |
| rs145215764 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148058804 | TGGGGTTTGGCCCCA[C/T]TGCTGCACGTGAAAG | 79658 |
| rs145232116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147753180 | GCTGGAAATAAAACT[C/T]GTCTCCTGACTGCTG | 79658 |
| rs145234400 | snp | A/G | 0.000131867 | 0.00811889 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147966774 | CAGGAAGAAACTGTC[A/G]CTGCCCTCATGGACT | 79658 |
| rs145239556 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147823161 | TGGAGAAGCTGCTGG[A/G]CCTCTCGACCAAGGC | 79658 |
| rs145242661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147936236 | TATCGGGCTCAAAAG[A/G]TCTCTGATTTTTGTG | 79658 |
| rs145247214 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147756425 | GTTTCTCCATTAACT[G/T]CAGTTAATCAGCAGG | 79658 |
| rs145249842 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147893353 | GTGAGCCACTGCTCC[C/T]GGCAGGAAGTAAACT | 79658 |
| rs145250497 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147908183 | TTGTTGAAATTTTTA[G/T]CTGTGAATCAAGAGT | 79658 |
| rs145256834 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147952191 | CTTGCTTGTAACTTT[C/T]GGCTGTTGCACATAA | 79658 |
| rs145270238 | snp | C/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147830708 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCTTGT | 79658 |
| rs145284157 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148027344 | CTTGCAAGCCAATTG[G/T]CAAGATTTAATAACA | 79658 |
| rs145312098 | snp | C/T | 0.00120805 | 0.0245472 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147913040 | TGTGATAAATAATAA[C/T]TGTACACTTAATGTT | 79658 |
| rs145315009 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147829717 | ACTTATCTGAGGTGG[C/G]CAGCTGTCCAGGAAT | 79658 |
| rs145335700 | in-del | -/CT | 0.0170251 | 0.090679 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148046327 | ACCACAAAAGCCTAA[-/CT]CTCTTGTAGTACCCT | 79658 |
| rs145347045 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147832707 | TTTCTACATCACTAA[A/G]TAAGGTTGTGACAGA | 79658 |
| rs145347850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147788858 | ATGCTTTATTAAGCT[A/G]CAAGCTGTACAGCAA | 79658 |
| rs145365359 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148054005 | GAATTTTGTAGTAGC[C/T]TTTCCACTGCTTAAG | 79658 |
| rs145366754 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147846452 | TTACTAAGTATGTTT[-/T]CTTTTGATGAATATT | 79658 |
| rs145382568 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148005754 | TTTCATGATTGAGGT[G/T]CTTGTGTCTTGTCCT | 79658 |
| rs145399420 | snp | A/G | 3.29462e-05 | 0.00405857 | synonymous-codon, intron-variant, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148063220 | AACAAGCTCCAACTC[A/G]GCTGTGACACCTCTT | 79658 |
| rs145407935 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889262 | TTGTGGGTATTATAA[A/G]TGGATTTCTGATGCA | 79658 |
| rs145416099 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147962821 | GGTGCACACCACCAC[A/G]CTGGCTAATTTTTGT | 79658 |
| rs145423688 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147934544 | TGTGGACTTGTTTTA[A/C]GATGTACCCTGGTGG | 79658 |
| rs145435024 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147766884 | GAGTCTTGCTCTGTC[A/G]CCCAGGCTGGAGTGA | 79658 |
| rs145478033 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147949644 | GAAGGAAAGAGTAGG[C/T]AAGGGATATAAACAT | 79658 |
| rs145484621 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148060675 | GTTGCCCCGTCTTGT[C/G]AATATTCCAGCTTAC | 79658 |
| rs145485923 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148024013 | AATCGTTGCCACGTG[G/T]CCCTGTTGTTTCAGT | 79658 |
| rs145486516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148007040 | TTAGACGAAATTGCC[C/T]GTAGGTGCGGTGGGA | 79658 |
| rs145495596 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148008907 | TACTGTTAAGTCGGA[C/T]GTTAAAGAGATTTGC | 79658 |
| rs145509797 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147968265 | CTCCCGCTGTCTCAA[A/G]CCCCCTCAAAGTAAA | 79658 |
| rs145509889 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147893190 | CAGCCTCCTGAGTAG[C/T]TGGGATTACAGGTGT | 79658 |
| rs145545739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147938241 | GAAAAGGGAGGGGAT[C/T]AGGAAGAATAATTAA | 79658 |
| rs145549080 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147916371 | TACTTACTATTTTAT[A/G]GCATTTTTCTTAAGC | 79658 |
| rs145575765 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147973246 | GACCACTAGTGCCTG[A/C]GTTTTACATGGCTCA | 79658 |
| rs145576086 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147843999 | ATGAGGACAAAATTG[A/G]TATCTCTGACCTAGG | 79658 |
| rs145586405 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148019392 | TATGTCACTTAATCC[C/T]TGTAGTACAGGCATT | 79658 |
| rs145587355 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147808186 | CCAGTTACAAAGGCT[A/G]TCGGAGGTGAGCCCA | 79658 |
| rs145613659 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147904301 | GTTAGTTACATATGT[A/G]TACACGTGCCATGCT | 79658 |
| rs145616013 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147951173 | AACTTGTAGAAGATA[C/T]TCAGATACAAATTCA | 79658 |
| rs145618250 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147898954 | TCACCTTATACCTTA[C/T]ACCAGATCCCTTTCT | 79658 |
| rs145634775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147771385 | CTGTAATATTTTGAT[A/G]CAGGCATGCAATGTG | 79658 |
| rs145641655 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147775179 | CGGCCCCCCAAAGTG[C/T]TGGGATTACAGGCGT | 79658 |
| rs145700164 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147849088 | AGAGCCCGTCATTGT[A/G]GGTCATAGGGAGAAG | 79658 |
| rs145720035 | snp | A/G | 0.000642626 | 0.0179137 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147866779 | TTGCCAAAGACTTCA[A/G]TCACTACAAAATGGA | 79658 |
| rs145731431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148013822 | ATGTATTTACTTATA[C/T]TCAGTTTAAAGTTTC | 79658 |
| rs145736750 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148020154 | TGGGATATTCAGCCT[A/T]TACAACATAGAGCTT | 79658 |
| rs145738189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147974468 | TTCTTTTAATATCTG[C/T]CTTAATACTGAAAAA | 79658 |
| rs145752870 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147788704 | ATCTCAAATGATATC[C/T]ATGCTTGATCTCTCT | 79658 |
| rs145770360 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147951135 | CTGCATTGCCTAGCT[A/G]GACATATGGCAATGA | 79658 |
| rs145772388 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147740304 | CTCAGTGAATTCAGA[C/G]AGATTAGTAGCTTGT | 79658 |
| rs145785619 | snp | A/G | 0.02016 | 0.0983543 | | | GRCh38.p7 | 4:147746579 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 79658 |
| rs145790518 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147737291 | AAGTAGCTGGGATTA[C/T]GGGCACGCGCCACCA | 79658 |
| rs145831017 | in-del | -/TCT | 0.0501905 | 0.150254 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148050679 | TGCCCGGTTGATTCA[-/TCT]TCTTTCTTATAAAGA | 79658 |
| rs145852026 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147980913 | TTGTTATTTTTGATT[A/G]TGCTTATTTGGATCT | 79658 |
| rs145868529 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147927062 | CAACTTGCTTCCAAG[A/G]CTGTGTTTTAAATAC | 79658 |
| rs145869649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147843825 | GGCCTGAACCCCTTT[C/T]TTCTTTTATCCAACA | 79658 |
| rs145877320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147985638 | AATATTTGATCCAAG[A/G]CTAAATTGTCTGCAT | 79658 |
| rs145885728 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147954765 | TATGTAACTTGTTTT[C/G]TAGACTCTGAAAATG | 79658 |
| rs145887773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148030347 | TTGAAACTCTTGTGG[C/T]GTAGGAGGTAGCTGG | 79658 |
| rs145893430 | in-del | -/GA/GAGA | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148059973 | TAAAGCCCACTCTTT[-/GA/GAGA]GAGAGAGAGAGAGAG | 79658 |
| rs145907402 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147909508 | TGTGACCAAAAGGAT[A/C]TTGTTATGAATAACA | 79658 |
| rs145911372 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147831815 | CACAGTCAGGAATAA[C/T]TCAAATCAAAATTCT | 79658 |
| rs145913155 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147862507 | GGGCACCATGGAGTG[C/T]GCAGCCCTGGCTGCA | 79658 |
| rs145916567 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147914607 | ATTTTTGTACAAATG[A/G]AATCATGCAGTTCAT | 79658 |
| rs145928453 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant, nc-transcript-variant | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147782634 | GCCAGTCCTGAGATG[C/G]AGGGACTGGCATGCT | 79658 |
| rs145940753 | in-del | -/C | 0.0295035 | 0.117819 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148038418 | GCAACATTTTATAAT[-/C]CCCCCCCATTTCAGG | 79658 |
| rs145950581 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148005107 | TACACTTCAGGCACA[C/T]TGGCCTATTTGGTAT | 79658 |
| rs145957554 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147789181 | GTCGTGGAGAAGTCA[A/G]TTCAACTGTAAGCTT | 79658 |
| rs145966316 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147745324 | CCATCCAAATACTTC[A/C]AAACATTCAACCCTG | 79658 |
| rs145969467 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147962549 | TCCCAGGTGTAGTGA[C/T]GGTCCTGACATACAA | 79658 |
| rs145972649 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147966292 | CAGCTACTGATCAAA[A/G]ATCCAGTATTCCCTG | 79658 |
| rs145985610 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147840976 | GCAAACAGTGACCCA[G/T]GGGCCTGACCTACCT | 79658 |
| rs146004459 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147798326 | GCTATTATTATTTGT[A/G]TTTTTGTTTTATATG | 79658 |
| rs146005397 | snp | C/T | 0.0103295 | 0.0711199 | upstream-variant-2KB | ARHGAP10 | GRCh38.p7 | 4:147731329 | ACCTGGCATGTTTTC[C/T]GGTAGTTATTTTTAG | 79658 |
| rs146024064 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147929473 | TTTGTGTATGAACCT[A/G]TTTATTTTTATGTAA | 79658 |
| rs146024674 | snp | C/G/T | 9.91412e-05 | 0.00704003 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147857596 | CAGAAAAGAATTATA[C/G/T]TCTAATTGATAAACA | 79658 |
| rs146039785 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147734327 | ATCTGGGGGGCCAGA[A/T]GTCAGCTTTCCTCCA | 79658 |
| rs146044277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147801533 | TGTTCCAATTTTAGT[A/G]TTCATCATTTTTTGT | 79658 |
| rs146071495 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148022542 | CCTCTGTGTGATATG[C/T]TTTCTTTGTGGCACA | 79658 |
| rs146087299 | in-del | -/TG | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147999317 | CATTTGAGCCATCAA[-/TG]GCTACCCTCTTTGGG | 79658 |
| rs146089933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148026357 | AACCCAGCATGAAGC[C/T]GGAGGGGAGATCCTC | 79658 |
| rs146090111 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147907078 | GAGATGGAACAGGAA[A/G]TGTGAGATAGTGCAG | 79658 |
| rs146090538 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147984754 | AGGCCAAGAAGTGGC[G/T]TTTGGGTTAAGAGCC | 79658 |
| rs146091556 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147748703 | AGGCTGGGCACTGTG[A/G]CTCAGGCCTGTAATT | 79658 |
| rs146094224 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911493 | TCAACCTCCCGAGTA[A/G]CTGGGACTACAGGTG | 79658 |
| rs146109762 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147786469 | AAATCTGTAGGAAGG[A/G]TTTTCTTTTTCCGCT | 79658 |
| rs146113438 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147866168 | AGATTTATTGACTTA[C/T]ATGTGGAGCAGAGGC | 79658 |
| rs146129377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147746352 | TGTGATCCGCCCGCC[C/T]TGGCCTCCCAAAGTG | 79658 |
| rs146148103 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147871701 | TTGTAATTAGAAGAT[A/G]CCTTCATATGTACTT | 79658 |
| rs146182672 | in-del | -/TTTATAT | 0.0379877 | 0.132479 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147858169 | GTAAGCAGGAAGGAA[-/TTTATAT]TTTATTTTTCATTTT | 79658 |
| rs146192609 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148046687 | CTTGTAAGGAAAACA[C/T]TCCTCGCTGTGTATT | 79658 |
| rs146197552 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148038540 | CCCTACCTCCTGAAC[C/T]CTCGTCTTCCAATAC | 79658 |
| rs146211426 | in-del | -/ATTAA | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147771497 | TTTTAAAATGTATGA[-/ATTAA]TTATTTTTGACTATA | 79658 |
| rs146212307 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147926488 | GATGAGACCTTTAGC[C/T]AAGGCAGAATGCAAG | 79658 |
| rs146218680 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148004206 | AAAATAAAAAATTGA[C/T]TTAAGCTTTGAAGGG | 79658 |
| rs146231301 | in-del | -/GGTTTTT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147901668 | GAAATAATATGGCTG[-/GGTTTTT]TTTAATCTGAAGCCT | 79658 |
| rs146247967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147765430 | GTGTCTATTGTGTTA[C/T]GTCTTCTGATTAAAA | 79658 |
| rs146281820 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147768236 | CTCTGGGCCCTCCCC[C/T]TGGTTCCTGCTCCCC | 79658 |
| rs146315403 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148069213 | CTTATCTGCAACTGC[A/G]GAGCCACTTTTCCTG | 79658 |
| rs146318020 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148017729 | GAAGTGTGATATCAT[C/T]ACATAGATAGATACT | 79658 |
| rs146330400 | in-del | -/C | 0.481473 | 0.0944461 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148001648 | CTTGTAAGTTGGATT[-/C]CTAGGTATTTTATTC | 79658 |
| rs146332468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147944722 | GGTCTTAGTTAAGAC[A/G]TCATCGTGGAGTGAG | 79658 |
| rs146332732 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147947036 | GAATTCATTGTGTCT[G/T]TATATTTTATGCTGA | 79658 |
| rs146349439 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147821422 | GTGCTTTTCTTCTAT[A/G]CTTTAGGTGTAAGAA | 79658 |
| rs146369976 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147780938 | TTGTCCTCCACCTCC[C/T]ACTTTTGGGAGAATG | 79658 |
| rs146386356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911309 | GCCAAGGATTAGTGT[C/T]ACTGTTCCCTAGGTT | 79658 |
| rs146423921 | snp | A/G | 0.00014859 | 0.00861816 | synonymous-codon, intron-variant, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148063283 | TCCTGCTACTGTAGC[A/G]GACAAGCCACCTGAA | 79658 |
| rs146427370 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148044112 | ACTTGAGGGTTCAAA[G/T]TGCCACTGTTTGGCA | 79658 |
| rs146434083 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147958567 | TCTTGCTGGGGAAGG[G/T]CTTAGGAACCCAGGA | 79658 |
| rs146448366 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147834730 | CACCCACTTCCACCC[A/G]CACACCCACCCACCT | 79658 |
| rs146449829 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147761389 | CTCCTTTTAGTAGTA[A/T]TCGCTGTACTGACCA | 79658 |
| rs146466221 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147839114 | TCTATCTATCTATCT[A/G]TCTATCTATCTATCT | 79658 |
| rs146504736 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148014496 | ATCAGGAGAGGTTCA[C/T]CTGATATAGATGGGG | 79658 |
| rs146518778 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147898970 | ACCAGATCCCTTTCT[C/T]GACATGTGGGGATTA | 79658 |
| rs146524025 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148018744 | TGGTAGTATTTTTCC[C/G]TAAGAATTAAATGTT | 79658 |
| rs146525702 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147923311 | TAAGTACAAATGAGC[C/T]GCCCCCCATGAGCAG | 79658 |
| rs146557209 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147903131 | TGGCCAGGGAGGCCC[C/T]GTGTGGCTGGACCCC | 79658 |
| rs146557839 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147979207 | ATTCAAGTCTTGACT[C/G]CATCTTTAGTTAATT | 79658 |
| rs146575703 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147855752 | AGTAGAAAAGGGAAG[A/T]AACCTCAGTTCCTGA | 79658 |
| rs146578995 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147860577 | ATAGCTTCTACCTCC[A/G]TCCACACCCCTACAT | 79658 |
| rs146590460 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147740809 | TAGAAATATAAAAAG[A/G]TAGTCTCACAATAAA | 79658 |
| rs146594549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147744534 | GTTGTGCAAATGAAT[C/T]GGAGGAAAGCAGGAC | 79658 |
| rs146631700 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147928235 | TACTTCCAAAAATAC[A/G]GGTTTAGACCCAGAA | 79658 |
| rs146641970 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147995080 | TCTATGTGTTTTTAT[A/C]CACATTCTATGTAAC | 79658 |
| rs146642017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148041995 | CGTGACTTTCAGATC[A/G]ATAAAACTATCCCAG | 79658 |
| rs146656424 | in-del | -/CC | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147853782 | ATGGCTTCTTTCTTT[-/CC]TTTTTTGCTTAGAAG | 79658 |
| rs146657578 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147880120 | GGAAAGGTGATCTTT[A/G]TATGTATTTTAAATG | 79658 |
| rs146660744 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147885861 | TTTCCTTACCCTTTT[C/G]TGTGTTTTGAACTGC | 79658 |
| rs146674603 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147997344 | CTAAAATTAATCTCT[A/G]TAGAACTATTCAGTA | 79658 |
| rs146688350 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147796089 | GAAGACCTAGAGCTA[C/T]TTGTTTATAATTTCC | 79658 |
| rs146693616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147878236 | GAGTAGCTGGGACTA[C/T]AGGCGCGTGCCACCA | 79658 |
| rs146698043 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147882537 | TGAAGAGAACAATGG[C/T]GAGAGGAACTGGGTG | 79658 |
| rs146706705 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147799355 | ATTTGCTCAGCTTCT[G/T]AAATCTGTTTATGTC | 79658 |
| rs146707582 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147756070 | TTCTAAAAATTTCTT[A/G]CCTTTTTCCTCATGG | 79658 |
| rs146741554 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147979784 | CCTGGGTTTTTGTGT[A/T]GGTGTGTGGCTATTG | 79658 |
| rs146746076 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148060085 | CTCTTGGAACCCAGG[C/T]TGAGGAAAAGCTGTT | 79658 |
| rs146749474 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147800774 | GAGCAGAGAGACATA[A/G]TTTTCTATGCTGTCT | 79658 |
| rs146763352 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147937466 | AGATGAATTTGTGGG[A/G]ATACAATTCAGCCTA | 79658 |
| rs146767648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147762622 | GCAAGCTCTGCCTCC[C/T]GGGTTCACGCCATTC | 79658 |
| rs146777012 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147803119 | GTTCAAGCGATGCTC[A/G]TGCCTCAGCCTCTCA | 79658 |
| rs146780598 | snp | A/C/G | 0.00105501 | 0.0229446 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148064441 | CGGAAGGCTCGAGCC[A/C/G]TGTATCCGTGTGAAG | 79658 |
| rs146809197 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147813424 | TCTGTCATGGCCTTC[C/T]GTGGGAAAAACATGA | 79658 |
| rs146815309 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147897895 | TTTGAGACAGAGTCT[C/T]GCTCTGTTGCCCAGG | 79658 |
| rs146819937 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147901888 | ATTTTTCCTCCACAT[A/G]TGAGCATCAGTGGAA | 79658 |
| rs146827185 | snp | A/G | 0.000181577 | 0.00952656 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147879280 | ACTATTGCATGTATC[A/G]AAAAGCAGCAAAGAA | 79658 |
| rs146828659 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147774131 | AATAAATGTAAGGCA[A/G]TTTAGGATAGTGCCT | 79658 |
| rs146828736 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147817424 | AAAAATTGTTGATAA[A/G]TAGGTGGCTCTGCTA | 79658 |
| rs146864918 | in-del | -/TA | 0.142947 | 0.22592 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147852730 | TTTTTTTTTTTTTTT[-/TA]AAATGGAGCGGAGTT | 79658 |
| rs146866866 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147999227 | ATTAGGCAAAAACAG[A/G]AGGTAAATAAATAGC | 79658 |
| rs146874742 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147827478 | CTAAGCTTGTGGCTG[G/T]TAGGAAAGGGTTTAT | 79658 |
| rs146879762 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147878770 | TCTTATTTTCCTTCT[C/T]CCTCTTTTTTTTTTT | 79658 |
| rs146886056 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147954347 | CTTGTAGTTCTGTCA[A/G]TTTTTGCTTCAAGTG | 79658 |
| rs146891902 | in-del | -/AAACC | 0.0205511 | 0.0992634 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147898868 | CTGCCAAACACTTTT[-/AAACC]ACCAGATCTTGTGAG | 79658 |
| rs146908186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148062523 | TCAATTATTTGAACT[C/T]TCCCTCTGTGCTTAG | 79658 |
| rs146935682 | snp | A/C/T | 0.00835141 | 0.0640778 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147863479 | CATATGGATTGGCTA[A/C/T]ATTTTATTTACTCAT | 79658 |
| rs146937582 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148067052 | TCGTTCTGTCCCTCC[C/G]CTAAGGCTGGCTACT | 79658 |
| rs146965095 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147815331 | AGTAGAGTACCTGAT[A/G]TTATAAGGTGTGGTA | 79658 |
| rs146969846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147946262 | TACAACTGAAAGTGC[C/T]GCTTGCTATAAGCCA | 79658 |
| rs146989100 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147824982 | ACATTACCTTGCCCT[A/C]GATCACATGGCATCT | 79658 |
| rs146989372 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147779443 | TTGGCATCTCCTTTC[A/G]GTTAATTTGGTAGAT | 79658 |
| rs147018971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147782141 | TTGCCATAAGGTGAA[C/T]GTCCTGCAGAGAGAC | 79658 |
| rs147057515 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147886669 | TTCTCTCTTTCTAGA[A/G]AAGCAATTTCTACTG | 79658 |
| rs147057943 | snp | C/G | 0.0197687 | 0.0974348 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147959726 | GGTTGCATAGTATTT[C/G]ATGGTGTGTATGTGC | 79658 |
| rs147058138 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148006214 | GAAGCCCATGCTCAC[C/T]GTGTAGAGAGGCTAC | 79658 |
| rs147073766 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147837362 | AAATACTAATCCTTT[A/G]TTAGTCTGGATTCTC | 79658 |
| rs147087325 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147767537 | ATAAAGAAGACTGAG[C/T]CTATATTAAAAGATT | 79658 |
| rs147105632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147733412 | AGGATGGCGGTGAAT[A/G]TCCCCTTTCCCCCTT | 79658 |
| rs147116007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148016375 | GGTTGTGGTGGCACG[C/T]GCCTAAAGTCCTAAT | 79658 |
| rs147123190 | in-del | -/ATATATATAG | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147798809 | TATATATATATATAT[-/ATATATATAG]ACTTTTTACCCCCCC | 79658 |
| rs147131973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147976867 | AAATTGAAGGGCTCC[A/G]ATATAAAGTGTGCAT | 79658 |
| rs147132255 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147848898 | AAAGGAGAAATGGTT[A/T]CAATAGTTTATTCTG | 79658 |
| rs147132549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147900856 | CAACACGCCTTGAGA[C/T]AGGTTCTTGTTATTT | 79658 |
| rs147144123 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147776775 | GGCAGCATTGGGAGC[G/T]TAGTGCACTGGGACT | 79658 |
| rs147148587 | snp | A/G | 1.64751e-05 | 0.00287007 | missense, utr-variant-5-prime, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147822768 | GCTCATTCACTCAGA[A/G]ACTTTAAGTTTGAGT | 79658 |
| rs147162744 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147852648 | GTTTTACCATGGGCC[A/G]ATTGACGTAAACAAA | 79658 |
| rs147173903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147739249 | CAGTGGTATCTTGGG[A/G]AAATATTTTCTAGAA | 79658 |
| rs147203598 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148027361 | AAGATTTAATAACAT[C/T]TGAGTGTTGGTCTTA | 79658 |
| rs147206747 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148032853 | CTCATGTTCGAGGGC[A/G]GGAAACATCCAGCTT | 79658 |
| rs147216107 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147957094 | TTTGCTTCCTGACTT[C/T]GTGGGAATGCTGTGA | 79658 |
| rs147221950 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147915810 | GAACTTATTATTGAA[A/C]ATGATGAGGACAGCT | 79658 |
| rs147228885 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147832923 | TTTGGACAACTGTAG[C/T]TCCTCAGTATTTCAG | 79658 |
| rs147249006 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147794883 | TAACCAGTTCCCCTT[A/C]TGATAGACATCTAGG | 79658 |
| rs147280646 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147797290 | AAGATCCAACCTCTT[A/T]GCCAGGTCTTTACAC | 79658 |
| rs147280759 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147754253 | TTCTTGTTCTGTTTC[A/C]AGGTGTCATTTACAT | 79658 |
| rs147295944 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147758023 | TAAACGTTACATTAG[A/T]TAAAGGAACTGTTTT | 79658 |
| rs147305932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147973462 | TTTGATAGAGGCATG[C/T]CATGGGTAATAATCA | 79658 |
| rs147310500 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148050986 | AAGGAATGGAGTCCA[A/G]ATGTATGTGGATCAC | 79658 |
| rs147313857 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148055829 | TCTGCTGCAGGAAAG[C/T]ACTGGGTATGTGTGG | 79658 |
| rs147326065 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147935352 | AATAAAAAGATAGAA[A/G]ACAGTGTTCAGAATG | 79658 |
| rs147328909 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147982707 | CACCTAGCCTGGATT[C/T]CTTATATCTGCATTT | 79658 |
| rs147337502 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147852918 | AGATGGGGGGTTTCA[C/G]CATGTTGGTCAGGCT | 79658 |
| rs147340653 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147805385 | GTAGCCATGTTGTAC[A/C]ATTTGAAGTCAGGAA | 79658 |
| rs147340847 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147860142 | TCTCCTCTTGCTTCA[A/G]TTGAAAATAACAGGA | 79658 |
| rs147342934 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147939445 | TGTACTAATCATCAC[C/T]GTATTTTTAAAAGGC | 79658 |
| rs147356610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147810243 | TAGTTGGCCATCTGG[C/T]AAAAACTGTTATTTA | 79658 |
| rs147358803 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147742727 | CTGACCTCAGTGATC[C/T]GCCTCTCTCGGCCTC | 79658 |
| rs147413974 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147993550 | CTTTCTAGAAGTCCA[A/G]TATTTAGTGAGAAAG | 79658 |
| rs147430590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147996280 | ATAAACAGAAAGGCA[A/G]TCGAAAACAAAACAT | 79658 |
| rs147433754 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147951835 | TTATAGTGTAAGTTT[C/T]GGTAAGTTTGATATA | 79658 |
| rs147449928 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147955621 | TAAAGCCAAGACAGG[A/C]TTCTTGTCCCATGAG | 79658 |
| rs147462633 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147758295 | ATTTTGATGTAGTTA[C/T]GTATGAATAAACCTA | 79658 |
| rs147479325 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147832507 | CAAAAATTAGCCAGT[C/T]GTGGTGGCGGGCACC | 79658 |
| rs147492211 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147764002 | TCGGGTGATCTGCCT[A/G]CCTCGGCCTCCTAAA | 79658 |
| rs147519262 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148008830 | GGTGTTTTCCAGAGG[C/T]GATGATATTAAGACA | 79658 |
| rs147534648 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148012653 | CCTCAAAGTTTAGTC[G/T]TAATAGATATATTAA | 79658 |
| rs147545995 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147981822 | TGCTCTTACTTGTCC[-/T]TTTTTTTTACTGTTG | 79658 |
| rs147549980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147773183 | AAAAATAGCAGATTT[C/T]CCTTCTAAACATGCT | 79658 |
| rs147551361 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147733047 | TATGCTGCTTCCGCA[C/T]ATTCCTCCCCTGCCG | 79658 |
| rs147565214 | in-del | -/CCTCCTGCA | 0.00478085 | 0.0486577 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147922020 | GCCTTCTCCCCTGCC[-/CCTCCTGCA]CCTCCTGCACCTCCG | 79658 |
| rs147566643 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147735937 | GATTCATACAGGTAG[A/G]TAGCACAGTTGCCAG | 79658 |
| rs147574644 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148071519 | TACTCAGGAGGCTGA[A/G]GCAGGAGAATTGCTT | 79658 |
| rs147577411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148019814 | CTAACCTAACCTTCC[A/G]TAGCTGTTAAGATTT | 79658 |
| rs147592754 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147948897 | TGGGAACCCAGGAGG[C/T]GGAGCTTGCAGTGAG | 79658 |
| rs147593971 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148023689 | TGTGACCTCCTGTGA[A/C/G]GTTACATAACCCTGA | 79658 |
| rs147605845 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147825425 | GCACTCCAGCCTGGG[C/T]GACAGAGCGAGACTC | 79658 |
| rs147622223 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147952972 | CATTTTTGCATAGGG[A/T]TCTCCAGTAGTTCTA | 79658 |
| rs147624249 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147909042 | GCCTGAGTTCAGGTG[C/T]CCATCACAAGTCTGG | 79658 |
| rs147634895 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147829898 | AAATAAGGGCAATTG[A/G]TTGAGACCCAGAGGT | 79658 |
| rs147635342 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147782368 | CCACATGGCATATGC[A/G]TTTTATTATCAGCAT | 79658 |
| rs147640829 | snp | G/T | 1.64893e-05 | 0.0028713 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147913105 | GATGGGGTTCACAAT[G/T]ATCAGAAAATGCATC | 79658 |
| rs147651580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147789054 | GAAAACTGCAAGGTG[A/G]TGACTGCTTTTGTGA | 79658 |
| rs147655346 | in-del | -/AA | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148061467 | CGTTCCTTTTCTGCT[-/AA]AAAAAAAAATGGAGT | 79658 |
| rs147680878 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147964270 | GACAGCCCTTGTGCT[G/T]CAGTGCCCACTGAAA | 79658 |
| rs147684554 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148043748 | TGTGTATATATATGT[A/G]TATATGTATATATAT | 79658 |
| rs147696885 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147968522 | TTTCAGTGGGCTCAC[A/C]TGCATTCCTGAATCT | 79658 |
| rs147728960 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147927905 | GTGTGGGGCCCCAAA[A/G]GTTACTAATGAAATC | 79658 |
| rs147731839 | snp | A/G | 0.0685596 | 0.171987 | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147781242 | CCAGCTACTCAAGAG[A/G]CTGAGGCAGGAGAAT | 79658 |
| rs147733684 | in-del | -/TGTGTGTGTGTGTGTG | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147870929 | ACCAAAACTACAGAC[-/TGTGTGTGTGTGTGTG]TGTGTGTGTGTGTGT | 79658 |
| rs147737078 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147784679 | TATATTATATATTAT[A/G]AATATAAAATATATA | 79658 |
| rs147740379 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147800428 | TCTGCCCTATTGCAT[A/T]TGTCGAGGCTCCCCT | 79658 |
| rs147756709 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147802940 | AAGTGCGGACTGTGA[C/T]ATGTAAGGGTTTGGG | 79658 |
| rs147757806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147736826 | AATTATTAGAAGAAT[A/G]AGGTTGTATCCCAGT | 79658 |
| rs147773491 | in-del | -/A | 0.0205511 | 0.0992634 | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147781977 | ATTGATTTCTGAAAT[-/A]ACGGTAAAATAAGTG | 79658 |
| rs147787565 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147986010 | GTTGAAGTGGATTTC[C/T]GTTTTCCTGTTTGAA | 79658 |
| rs147804312 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147989949 | TAAGAAATTACAAAA[G/T]TATTAATTTGGGGAA | 79658 |
| rs147815782 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147869757 | CCTTCAGTATTGAGA[A/G]CACCTGATCTAGGTG | 79658 |
| rs147817597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148070791 | CGCTGGAGTAGCTCA[C/T]GCCTCCCCTTTCCTT | 79658 |
| rs147820298 | in-del | -/A | 0.0103295 | 0.0711199 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148026664 | CTAGTTTTCTTAAAT[-/A]TAGAGCAGCTGTTAA | 79658 |
| rs147833497 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147946004 | CTCCACCCTGTTCCC[C/G]CAGTGCGCGTGTGGG | 79658 |
| rs147844528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147819652 | TCCCGGGTTCCTCCC[A/G]GGTTCACACCATTCT | 79658 |
| rs147849731 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147948551 | CCTGGGTCATTTTTG[A/T]TTATATCTTCATGAT | 79658 |
| rs147858413 | in-del | -/TTTTTC | 0.0704125 | 0.17392 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147843518 | CAGCTGAACTCCTTT[-/TTTTTC]TTTTTCTTTTTCTTT | 79658 |
| rs147861371 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147824576 | CCGCATTGCTGGGGA[G/T]GCCTCGGGAAACTTA | 79658 |
| rs147861889 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147752175 | GGCATGAGCCACAAC[G/T]CCTGGCCAAGCCTTT | 79658 |
| rs147863550 | in-del | -/AC/CA | 0.0275645 | 0.114116 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148030001 | CTCAGCATCCCCCCC[-/AC/CA]CCCACCAACCCCAAT | 79658 |
| rs147889806 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148048486 | TAAATCCTACATTAC[G/T]AGGTATGCTTGTCAC | 79658 |
| rs147908751 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147932620 | ACACATGGACACATG[A/G]GGGGAACAACACACA | 79658 |
| rs147908868 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148005938 | GTGAAACAAATACAT[A/G]TATCTCTTAGTGCAG | 79658 |
| rs147923033 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147803401 | AATGTGTAATGATCA[A/G]ATCAGGGTAATTGGG | 79658 |
| rs147955904 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147892775 | TTCTCAACTGTGGGC[A/G]ATGTTGCTCCTAGGG | 79658 |
| rs147969333 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147769537 | ACTGACATTGTTTCC[C/T]GGGGATTTCCGTATG | 79658 |
| rs147972776 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147785435 | AGCTGTATTGTGCCC[A/G]TCAGATCAATAGTGT | 79658 |
| rs147976084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147986472 | CTTTTCGAGAAAATC[A/G]AGGGGTTAACTGATT | 79658 |
| rs147984109 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148049462 | GCGTTGCTGTCCTCC[C/G]AGTAGCCGGTGTGTG | 79658 |
| rs148003891 | in-del | -/TTAGCCCCAGCTC | 0.0596104 | 0.162024 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147733338 | GAAAATGGGGCGGAA[-/TTAGCCCCAGCTC]TTAGCCCCAGTGAGG | 79658 |
| rs148012998 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147980667 | TCCATCTCGTCCAGG[G/T]CTTTTCTTGGTTGGT | 79658 |
| rs148015211 | snp | A/G | 0.000181253 | 0.00951808 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147906699 | AAGCAGTGGTTGGAA[A/G]CTCTGGGTGGAAAGG | 79658 |
| rs148034415 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148045782 | AAATCCATCTAAGAT[A/G]TTTTTTGAGAGCAAG | 79658 |
| rs148042189 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147938438 | GGAACAAAACTTGAC[A/G]AGGAAGAATGAATGC | 79658 |
| rs148042771 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147856972 | ATTCTCACGCCTCAG[C/T]CTCCTGAGTAGCTGG | 79658 |
| rs148047649 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147923929 | AAGGGCAATGAAGAA[A/G]ATAAAGAACAGCTGT | 79658 |
| rs148054778 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147741951 | GAATTTCCTCCCTGT[A/G]TTTCCTCAGAAAGAC | 79658 |
| rs148110785 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147890012 | TCACCTGAGGCACGA[A/G]ACAGCATATAGCACT | 79658 |
| rs148112543 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147803762 | TGTAAATTACAGCAT[G/T]TTATTCTTTTCTGTG | 79658 |
| rs148116064 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147767694 | TGAATAGCCACTGCA[C/G]TCCACTCTGGGCAAT | 79658 |
| rs148150074 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147828514 | AGTGATTCATCCATT[G/T]GAGGAGATGGCTGAA | 79658 |
| rs148159646 | snp | C/T | 0.00597247 | 0.0543191 | downstream-variant-500B | ARHGAP10 | GRCh38.p7 | 4:148073176 | CTGCCTTCCAGGCCT[C/T]CCTGCTAATCTCTCC | 79658 |
| rs148172573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147946804 | CAATAGTTAAATTAA[A/G]CCTTATTTTAAAAAG | 79658 |
| rs148177029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147762269 | TTCCTCAGCCTCTCA[A/G]AGTGCTGGGATTACA | 79658 |
| rs148191887 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148054853 | TTGTAAGTGATTGGT[A/G]GATTTTTCTGAGCGG | 79658 |
| rs148194587 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148007961 | AATGTAATGCCCTAG[C/G]ATGTCCCAGTCAATC | 79658 |
| rs148202174 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147820446 | AACCGCCACCACGCC[C/T]GGCTAATTTTTGTGT | 79658 |
| rs148213515 | snp | A/G | 9.88435e-05 | 0.00702937 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147822776 | ACTCAGAGACTTTAA[A/G]TTTGAGTTTATCGGT | 79658 |
| rs148223831 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147942828 | TAAGGCAGCTATCCG[C/T]TGGATTTCCAGCAGC | 79658 |
| rs148237673 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147815051 | AGTCCACAGTCATTA[G/T]GTTGAGACTTCTGAG | 79658 |
| rs148253342 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147899329 | TGTGTGTGTGCATGC[A/G]TGTGTGTGTGTGTGT | 79658 |
| rs148258521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148003944 | GAAGAAAGCTGCAAA[A/G]TTATGCTAAGAGACG | 79658 |
| rs148261669 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147960366 | ATATCATTTCTCATT[A/C/T]TCAAATACTATTATT | 79658 |
| rs148262609 | snp | A/G | 0.021333 | 0.101051 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147887604 | CGGTGGCTCATGCCT[A/G]TAATCCCAGCACTTT | 79658 |
| rs148267526 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147775781 | TTATGGTATAAAACA[A/G]CATGTATGCAGCACA | 79658 |
| rs148314639 | snp | A/G | 0.000645957 | 0.01796 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147955422 | TTTGTAGTTGGTAGT[A/G]AGCATAAACGAAAAA | 79658 |
| rs148315965 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148031811 | AACACTGTAACAAGC[A/G]TGGGCCCTCCAGGAG | 79658 |
| rs148319788 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147770842 | CTGGGCAGCTTAAAT[A/G]GCAGTCTTATTTTCT | 79658 |
| rs148324884 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147845685 | CAGAAGACATATTAT[A/T]TGGAGGTTTATTTGG | 79658 |
| rs148329001 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147915042 | TCTGTATTCCAGTCC[A/G]ACTTTGGATGCCTTA | 79658 |
| rs148329610 | in-del | -/T | | | upstream-variant-2KB | ARHGAP10 | GRCh38.p7 | 4:147730867 | AATGAACTATTAGTG[-/T]TTTTTTTTTAAGAAA | 79658 |
| rs148336281 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147733835 | TTGGTTCTCTGACCT[C/T]TTTGGTGTTGCAAAA | 79658 |
| rs148368033 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148024749 | TCTGTCTCTTTCTTA[C/T]GTTCATTCTTTCTCA | 79658 |
| rs148383039 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147910377 | TTGTACAAAATACTT[A/T]CTCTACATTTACTTT | 79658 |
| rs148414873 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147971864 | AAGGCTAGGAGAGAG[C/G]TTATTTGGCATAGTC | 79658 |
| rs148417114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147929881 | TTTGTTGTATAACCC[A/G]TAGAGAAATCTGTCT | 79658 |
| rs148419453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147958281 | CATGGTGCTTAGTAC[A/G]AGAATGACAACTAAA | 79658 |
| rs148431644 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147735285 | GCACTGTGCTAAATT[A/C]TTGAAGAAACAAAGG | 79658 |
| rs148434383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147802332 | TGTTCAGAAGTTAGG[A/G]TGAAGCTTCTTAAAA | 79658 |
| rs148449106 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147916374 | TTACTATTTTATGGC[A/G]TTTTTCTTAAGCTAT | 79658 |
| rs148474147 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148026806 | AAAGCAAAATATGAC[A/G]TAGGCTGCTAAGTGC | 79658 |
| rs148482995 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147797725 | CAGCCAACACGCCCG[G/T]CCCCCTCCCCATTTT | 79658 |
| rs148485230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147881188 | CTGAGTCACAGAGTT[A/G]CTTGAACCCAGGATT | 79658 |
| rs148488452 | snp | A/G | 1.64898e-05 | 0.00287135 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148047027 | TGGCAGATGGAGGGA[A/G]CTTTGGAGACTGGGC | 79658 |
| rs148498827 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147758912 | TGTTCCTGGGAGGAG[C/G]AGGTTGCGGTGAGCA | 79658 |
| rs148503416 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147989274 | CAAGTGGAGGCAGGG[C/T]GAGATCACAGGACCA | 79658 |
| rs148515090 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147788767 | GTATTTGCTGAGAGC[G/T]CTAATTATCAGTACT | 79658 |
| rs148520598 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147867736 | GGGTGTGGTGGAGTG[C/T]GCCTGTAATCCCAGT | 79658 |
| rs148551630 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147753973 | CATCTGCTACTACTC[A/G]TTCTAAGAAAGACCT | 79658 |
| rs148556057 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147984309 | CCCAGGAAGCAGTTT[C/G]TTTCAGCCCAAACTC | 79658 |
| rs148557499 | snp | C/T | 0.0008772 | 0.0209244 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148063333 | GAATGTGGAATATGG[C/T]GGCAGCACACACAGG | 79658 |
| rs148570475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147940156 | TTCCTGTGCTTGCTT[C/T]TCACAGGGAAGTGGC | 79658 |
| rs148575066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147811309 | CATTCTTTTAACACA[C/T]TGGCTTCTGAAATAA | 79658 |
| rs148584538 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147744294 | AAAATGCATCTGAGA[A/G]GTCAGAGAGAGCACA | 79658 |
| rs148624897 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147935111 | AGCCTGAATGTAGCC[A/G]CAGAGGATGCAATGA | 79658 |
| rs148627872 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147891342 | GCTAAGTGAAAGAAG[C/T]CAGTCATAAAAGGCC | 79658 |
| rs148630470 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147997041 | AATAACCATTCTCTC[A/T]TGTGACAGAACACTG | 79658 |
| rs148636304 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147805123 | TTTTACATTGAAGTC[C/T]TTAATTCATCTTGAG | 79658 |
| rs148638243 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147768820 | CTCTGTTCACTGCAG[A/C]CTCCGCCTCCTGGGT | 79658 |
| rs148659989 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147953000 | CTAGTACGATTTGTA[G/T]GAGTGGCTATTTCTC | 79658 |
| rs148660321 | snp | G/T | 0.0197687 | 0.0974348 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147878155 | GGCTGGAGTGCAGTG[G/T]CGCGATCTCAGCTCA | 79658 |
| rs148691691 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147764594 | GGTGGAGTGCAGTGG[C/T]GTGATCTCAACTCCC | 79658 |
| rs148696914 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147837972 | AGGTATGCATATGTA[C/T]ATCTGCTAGATAATC | 79658 |
| rs148713596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147948313 | AAAAGTCATTTTTAA[A/G]AAGTCAGTCAAAATA | 79658 |
| rs148714596 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148022611 | GAGCAGCACATTTTA[A/G]TTAATGTTGTTATTA | 79658 |
| rs148716174 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148058883 | GTTGACTCTTTTTAA[A/G]GAAGAGAGTTTCCTC | 79658 |
| rs148724702 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147823395 | GTGTGGAAAGGGAGA[A/G/T]AACTTGGGCCTTGGA | 79658 |
| rs148727477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147907823 | CTTACCATATTTGGG[A/G]TGCATTTAGCCTCTG | 79658 |
| rs148741613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147781394 | ATTGGGCTGGACCTG[A/G]CAAGCCAGGATGTAG | 79658 |
| rs148760036 | in-del | -/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147945074 | TGTGGTGGTATGGCT[-/G]GGGCCAGGTTGTTAG | 79658 |
| rs148771721 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147977693 | TTTGGGGGTACATGT[A/G]CAGGTTTGTTACAGG | 79658 |
| rs148779661 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147791543 | GTGTGTGCGCGCGCG[C/T]GCGTGCGCGCGTGTA | 79658 |
| rs148783630 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147901559 | TCTCTGCTGGCTTCC[A/G]CAAAGGGCTGTGTGG | 79658 |
| rs148786381 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147853159 | GCATGATCCCACACT[C/T]GCTCACACAGTACTA | 79658 |
| rs148794136 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147777218 | TGCTAATTGAACTAG[A/G]GTCTGTGTGGCTGGA | 79658 |
| rs148798921 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147740027 | AGGTGTGAGCCACTG[C/T]GTCTGGCCTTACTGG | 79658 |
| rs148815511 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148039579 | TGCTGGGATTACAGG[G/T]GTGAGTCACCACACC | 79658 |
| rs148820926 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147949913 | TAATAAACTAGAGGC[C/T]CTTTTTATTTAGTAC | 79658 |
| rs148826925 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147909914 | ATTACACGTAATAAT[C/T]CTCTATTGCATGTGT | 79658 |
| rs148834481 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147826664 | GCCTCAGACCAGTCT[C/T]GTTTCTCCTGTGATC | 79658 |
| rs148875823 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148019443 | GAGAAAATGAGATAC[A/G]CTGTGTTAAGAAATA | 79658 |
| rs148878848 | snp | A/T | 0.140581 | 0.224783 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147905140 | GATATTAGCTCTTTG[A/T]CAGATGAGTAGGTTG | 79658 |
| rs148878945 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147979796 | TGTAGGTGTGTGGCT[A/G]TTGTAAATGGGATTG | 79658 |
| rs148883265 | in-del | -/ATAGG | 0.00478085 | 0.0486577 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147831390 | TGCTTGTGAGTTCTT[-/ATAGG]ATAAGTACCTAAGGC | 79658 |
| rs148892505 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147779294 | CAGGGACCACTCTTG[G/T]CAGGTGTGCACTGCG | 79658 |
| rs148895450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147856518 | CACCTGGCCTCTTGC[C/T]CTCTGATGGTTCAGT | 79658 |
| rs148931719 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147974582 | TTGAGGGTTTTAATT[A/G]GATTTTCAATGAGAT | 79658 |
| rs148936757 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148047408 | GCTGATGGACAGACT[C/G]TTGAAACTGTCTGTA | 79658 |
| rs148943062 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147850035 | GCTCTGTATCTAGCC[A/T]AAGGTTTGTAAATGC | 79658 |
| rs148944783 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147897304 | GATGGGGTTTTGCTA[C/T]GTTGCCCAGGCTGGT | 79658 |
| rs148945751 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147932631 | CATGGGGGGAACAAC[A/G]CACACTGGGACCTGT | 79658 |
| rs148952950 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147747322 | AGAGAAGAGGAGGAA[C/T]AGAAATTGTAAGAGT | 79658 |
| rs148959183 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147803416 | AATCAGGGTAATTGG[A/G]ATATCTATTGCCTCA | 79658 |
| rs148961403 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147737943 | TGTTCTCAGTGTCTT[C/T]TTGTCACATTGCCTT | 79658 |
| rs148963663 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148036727 | AGTTGACTAGCATAC[A/G]GATAGATGGAGAGGG | 79658 |
| rs148979681 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147995740 | TTTTTTTTTCATGAC[C/G]GAGTCTTGCTCTGTC | 79658 |
| rs149000263 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147927359 | AGGTGCATCCTTGGC[C/G]CAAGAGAGATGCACT | 79658 |
| rs149010385 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147800110 | CTGCCGTCTCATTTC[C/G]CCCTGCTGTTATTGC | 79658 |
| rs149029725 | snp | C/G | 0.0178098 | 0.0926698 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147885331 | AAAGAGGAGCAAAGG[C/G]ACATCTTACATGGCA | 79658 |
| rs149032117 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147990491 | GCCACTTGATGAAGC[A/G]GGCCTCTACAGAGGG | 79658 |
| rs149035054 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147870137 | CTCACTGCAAGCTCC[A/G]CCTCCCGGGTTCATG | 79658 |
| rs149041042 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147762036 | TTTTTGAGACAGAGT[C/T]TTGCTCTGTCACCCA | 79658 |
| rs149073856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148065673 | ATGGTAGTATTGAAA[C/T]GCACTCATTTGAGAA | 79658 |
| rs149085816 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147941989 | TCTTCCAAAAAAAGG[A/G]TTTTAGAGTTTTGAA | 79658 |
| rs149090789 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148048817 | CAAGAAGGGCTTGAT[A/G]TTTTTGGTCATAAAT | 79658 |
| rs149094525 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147755741 | ATATTTTTCTATTTG[A/G]CTCTTTTAGAAGCTG | 79658 |
| rs149097115 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147830078 | GAAGTGTCTTGTCCA[C/T]GGCTGCACCCCTTTC | 79658 |
| rs149140490 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148009416 | GGATTATAGCCATGA[A/G]GCGCCATGCCTGGCC | 79658 |
| rs149140992 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147936992 | TTGTGAACTGCACAT[A/G]TGAGTGATCTAGGTT | 79658 |
| rs149163480 | in-del | -/C | 0.0150606 | 0.0854603 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147734691 | TTTTGCGTCCAACTT[-/C]CCCCTGTCTACCTCT | 79658 |
| rs149169313 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147770617 | TTATGAAAAAAAGTA[A/G]TCAGTATATATTGAG | 79658 |
| rs149191158 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147955005 | GCTTTAAATACATTA[A/G]TGTGTAGAAGGAAGT | 79658 |
| rs149210419 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889363 | GCAGTGCAATGGCAC[A/G]ATCTCGGTTCACTGC | 79658 |
| rs149223822 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147766934 | GCTCACTGCATCCTC[C/T]GCCTCCCAGATTCAA | 79658 |
| rs149250407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148011185 | TTGATCCCTTGGTTG[A/G]GTGTTACTCTGGTTA | 79658 |
| rs149280230 | snp | C/T | 0.0644693 | 0.167566 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147970858 | TTCGGGAGGCCAAGG[C/T]GGGCAGATCACCTGA | 79658 |
| rs149281346 | snp | G/T | 0.0146672 | 0.084371 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148001192 | ttccccatttcctat[G/T]tttgtcaggtttgtc | 79658 |
| rs149293931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147772299 | CGTGTTTCCACCTGG[C/T]GGTAGTGTGTATCTG | 79658 |
| rs149296751 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147846788 | GAATGTAATTGAATT[G/T]TAAATTTCTAAGGAG | 79658 |
| rs149308358 | snp | C/G/T | 0.00019771 | 0.0099409 | missense, synonymous-codon, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148046998 | GCCTCCTGGACCAGA[C/G/T]AAAAACCACCTTCTG | 79658 |
| rs149319955 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147741790 | CACACACACACACAC[A/G]CGCACACACACACAC | 79658 |
| rs149329720 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147741584 | TTGTGGTAAGCCCCA[A/G]AGCAAACACTGGCAG | 79658 |
| rs149333806 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147965194 | TGGGTAGTGCTCTGG[C/G]ATTTGTGACGGGTGG | 79658 |
| rs149335252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148045066 | CTCCCCCACCCTCCC[C/T]GGGAACACACTTATG | 79658 |
| rs149339690 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148026746 | TTCATATAACATTTA[A/G]TCTCAACATCAAAGC | 79658 |
| rs149345367 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147840222 | TTATAGTTCTCTTGA[A/G]TCCCTATGATAGGAA | 79658 |
| rs149363736 | snp | C/T | 0.0126979 | 0.078662 | upstream-variant-2KB | ARHGAP10 | GRCh38.p7 | 4:147730593 | CTCCTGGTGCTGTTT[C/T]GTAACAAAAGGGCTT | 79658 |
| rs149393139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148021311 | CAAACTGGAGGAAAG[A/G]GGTGGGGCAGTTTTC | 79658 |
| rs149396380 | in-del | -/A | 0.0509478 | 0.151255 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147857963 | TTGCAGGAATAGATC[-/A]AATTAATTGGCTTTT | 79658 |
| rs149405506 | snp | A/C | 0.000313167 | 0.0125094 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147906640 | TGGTGTCTTTCAGGC[A/C]TGGCGTTTCCTTGAC | 79658 |
| rs149410227 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147983464 | TGCTGGGATTATAGG[C/T]GTGAGCCACTGCACT | 79658 |
| rs149414657 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147794832 | ACATGATTTTAATGT[G/T]CTTGTGGTGTTCTAT | 79658 |
| rs149418681 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147753611 | TGCCTGCCTCAGCCT[C/T]CCAGAGTGCTGGGAT | 79658 |
| rs149422176 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147860180 | GGGCGTGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 79658 |
| rs149461261 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147976455 | GCAAGAATATTTGAC[A/G]AATTTTCAGACTCCC | 79658 |
| rs149472806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147749792 | ATAAGAGAACTGAGA[C/T]GGTCAAACTAAATAT | 79658 |
| rs149476590 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147820331 | CATTCTCTAACCCAG[G/T]CTGGAGTGCAGTGGT | 79658 |
| rs149478400 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148054363 | AAAGGGGAATAATAA[C/T]ATCTGCCCCTCTGGG | 79658 |
| rs149493420 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147934693 | AATAGATTCAGCCTA[G/T]TGTGGTAGCATGTGC | 79658 |
| rs149503762 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147804914 | ATATTTTCTCCTATT[A/C]TGTGGGTTGTCTGTT | 79658 |
| rs149506195 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147739170 | CCAGCCTGGGCAACA[C/G]AGCGAGACTCTGTCT | 79658 |
| rs149538170 | in-del | -/TG | 0.0225045 | 0.103662 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147763182 | CTTTAAGAAAATGAC[-/TG]TTTTTTTGTTATATT | 79658 |
| rs149545220 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147929459 | CTTGGAAGAGTATCT[C/T]TGTGTATGAACCTGT | 79658 |
| rs149558711 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147801157 | TGAAAAATGTCAGCA[A/G]AATTTAGCATTTATT | 79658 |
| rs149561726 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147887245 | CAGTGCCCAGACACC[A/C]TGCCTTTCCTCCCTG | 79658 |
| rs149568943 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147948027 | CTCACTGCAACCTCC[A/G]CCTCCCGGGTTCCAG | 79658 |
| rs149574733 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147764201 | GAAAATACAAGGTCT[C/G]TTTGGGGTATTGATC | 79658 |
| rs149605957 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148068338 | TGGCCCAAATTAATC[A/C]TTAAAAGCCTCTGGC | 79658 |
| rs149609564 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147879679 | AGATATTTCTCCTAA[C/T]GCTATCCCTCCCCTA | 79658 |
| rs149620549 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147943836 | TGCTAGGGATGATTG[A/G]GCTATTTGAAAACAG | 79658 |
| rs149625521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147831917 | CCCATGACTCAGTGT[C/T]CTCTCTGTTGGTGAC | 79658 |
| rs149626021 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147757968 | AATACAAGCCTGGTA[C/T]GTGTGCCATAGCTTG | 79658 |
| rs149627030 | in-del | -/CTCT | 0.0696718 | 0.173152 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147937241 | TCTTCTGAGGCCTCT[-/CTCT]GGCATGGGGATAGCT | 79658 |
| rs149631390 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147817023 | TATGTGGCTCTCTAC[A/G]TAAAGAATATGAGCT | 79658 |
| rs149649450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147901454 | TGTTTTGAGTTATCA[C/T]TACATTATTTGCCAA | 79658 |
| rs149660485 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147777017 | CATCACTGATCTGAG[C/T]AACCTATGACTGGGC | 79658 |
| rs149664764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889199 | ATACTGTGAGCTCTA[A/G]TGTCTTCATTCTGCT | 79658 |
| rs149668378 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147766743 | ATATATATTATATAC[A/G]TAACTATATTCATGC | 79658 |
| rs149706344 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147957970 | AATGTAACTTTCTCC[A/C/G]TTAGCTGAATTCCAA | 79658 |
| rs149711304 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148070570 | GCTGAGTTGCAATTA[C/G]CATTCAAAGAATAAT | 79658 |
| rs149719568 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147833621 | ATATCTTAACAAAAG[C/T]AGTTTGCTTACTTCT | 79658 |
| rs149731265 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147734814 | GAGCTTTTGTATAAC[A/G]TCAGAGAGTCAAGGG | 79658 |
| rs149740164 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147945988 | CGGGAATTCCCAGTA[C/G]CTCCACCCTGTTCCC | 79658 |
| rs149741079 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148019157 | ACTTGATGTCCTTTT[C/G]CAGAGCACTTTAGAA | 79658 |
| rs149757292 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147903651 | CAACCAGTGATCTTT[C/T]TACTGTCTCTGTAGT | 79658 |
| rs149772480 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147829384 | AGTAGACATGAGGTT[C/T]CACCATGTTGGGCAG | 79658 |
| rs149794924 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148013685 | AGAGCGAGACTCCAT[C/T]TCAAAAAAAAGGAAA | 79658 |
| rs149806117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147897687 | ATATTCTAATTCTAC[A/G]TACACTATGAATGTG | 79658 |
| rs149811732 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147974430 | TGTGAAAAGCATCAA[A/T]GATCATATTAATCAG | 79658 |
| rs149823640 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147774069 | CCTCAGCTGTAAAAT[A/G]GGATAATAATAATAT | 79658 |
| rs149845039 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147780484 | GTGTTTATAGAGGTG[A/G]TGAAATGCTGTGCTC | 79658 |
| rs149853025 | snp | C/G/T | 0.00162974 | 0.0284997 | synonymous-codon, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148046962 | TTCCTCCCCGTCTCC[C/G/T]GTGACTACAGCTGTC | 79658 |
| rs149862273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147967581 | CTCAGCATATTAACT[A/G]CTAGAAATAAGTACT | 79658 |
| rs149867877 | snp | C/T | 0.021333 | 0.101051 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147927001 | CCTGAAGTGAAGAAA[C/T]GTGATTTGATTTGTC | 79658 |
| rs149873388 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147743280 | CCTCGTGATCCACCC[A/G]CCTCAGCCTCAAAGT | 79658 |
| rs149874981 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147843602 | CACGATCTCAGCTCA[C/T]CGCAACCTCTGCCTC | 79658 |
| rs149878599 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147799988 | GCCACCCAGTTAGTC[C/T]TAGCACACAGGTCCT | 79658 |
| rs149889123 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147732889 | CTCAAAAGAAATTTC[C/T]TGGGGATTCTTTGAA | 79658 |
| rs149893610 | in-del | -/ATG | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147950755 | ATACCAGCCCTCTGA[-/ATG]ATTTCTTATCTATGC | 79658 |
| rs149919898 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147919526 | GCAGTTGTTCCCAAA[C/T]TTTGCTGCACATTGA | 79658 |
| rs149920018 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147996637 | AGGCTGCATAGATGC[C/T]TGGCTGAATCCTCAT | 79658 |
| rs149933790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147795553 | CAAACGCAACTTCTG[A/G]AGTGTGAGCTCTTTG | 79658 |
| rs149949763 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147755546 | GGGAAAGAAAAAAAA[A/T]TACCAGTTCCATGTT | 79658 |
| rs149951002 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147985081 | GAGCTGCCTAATCTC[A/G]TCCAGGAGAGTGGGT | 79658 |
| rs149970276 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147941536 | GACATGAGTGTGACA[C/G]AACCTCACACATATT | 79658 |
| rs149984284 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147873359 | GCTTAAATAGAAGTG[C/T]GTGTACATGTTCACA | 79658 |
| rs149994997 | snp | A/C | 0.000429994 | 0.0146565 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147965040 | AAGCGGCAGCCCAGA[A/C]TCTCGTGTTAATGCG | 79658 |
| rs150001230 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147822641 | GAGGAGAGCTCTACA[C/G]CTTTACCAATTTTAG | 79658 |
| rs150002695 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147751911 | TTTTTTTTTAAGATG[A/G]AGTGTTGCTCTGCCA | 79658 |
| rs150005378 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148058151 | CTTCTGTCTTTATTA[A/C]CATTTTCAAACACTC | 79658 |
| rs150021827 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147936184 | CCCTTCTGGCTTCCA[A/G]AAAGAAGGAAGGATT | 79658 |
| rs150043333 | snp | A/G | 1.6473e-05 | 0.00286988 | missense, intron-variant, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148063200 | AACCCACAGTCTCCA[A/G]CCACAACAAGCTCCA | 79658 |
| rs150056541 | in-del | -/GGGAGTGTGGGGTTGGCT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147892574 | AGTTGAGCAGCATGG[-/GGGAGTGTGGGGTTGGCT]GGGAGTGTGGGGTTG | 79658 |
| rs150058302 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148050563 | TGTTTTTAGTAGAGA[C/T]GGGGTTTCACTGCGT | 79658 |
| rs150067243 | in-del | -/CT | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147914392 | TAAGATAGGGCCTCA[-/CT]CTGTCACCCAGGCTG | 79658 |
| rs150073877 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148005490 | TATGTATCAGTATTA[C/T]CAATTATTATGGCCC | 79658 |
| rs150075964 | snp | G/T | 0.000153988 | 0.00877328 | splice-donor-variant | ARHGAP10 | GRCh38.p7 | 4:147879340 | CTGGAGGGAAACTTG[G/T]AAGTATTTGATTCAA | 79658 |
| rs150091877 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147875529 | CTACCCTCATCACCA[A/G]TGCACACAGGCACAC | 79658 |
| rs150106292 | in-del | -/A | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147874026 | TCTTAGTTTGTGTTT[-/A]AAAAAAAAACAACAA | 79658 |
| rs150108273 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147949593 | TGATTCAAAATGTCA[A/G]TAATTCTGAGATTTA | 79658 |
| rs150113952 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148061398 | AATTTCCTGCCAGGG[C/T]TTCACTCACGCCTAC | 79658 |
| rs150115906 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147939117 | GCATCAAAAATGTCT[G/T]TTCGTCATTGATTTG | 79658 |
| rs150116979 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148010705 | TATCATGACTCTAAT[A/T]GTGGCCCGTAGTCCA | 79658 |
| rs150120962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147826210 | TGTTTCTGTTTTAGG[C/T]TCCTAGAAATAGAGC | 79658 |
| rs150132539 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147895119 | TTAGACTTTCCATTT[A/C]TCCCAGTAATGTTTT | 79658 |
| rs150167244 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148006734 | CATGTTATCTGCATC[C/T]TTTCATGTGATAAAA | 79658 |
| rs150172105 | in-del | -/TAAAT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147991161 | AAAAAAAAAAAAAAA[-/TAAAT]AAAAGAAAACAAATA | 79658 |
| rs150174356 | in-del | -/A | 0.0448719 | 0.142907 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147775433 | AATACCTGTTGTCTT[-/A]GGGGCCAGCTTCAGG | 79658 |
| rs150176177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147819475 | ACTATCAGTATTTGG[A/G]AATAGGTACATGAAA | 79658 |
| rs150183422 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147964803 | TGCAGCCACACTGAA[A/G]TTACCTCATTAGGGG | 79658 |
| rs150192600 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147778416 | CCATGACATGAGCCG[C/T]TTTCTCACAGTCCTG | 79658 |
| rs150197657 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147839852 | CTTACATCCGAATGT[C/G]TGACGAAAAAGGATT | 79658 |
| rs150199032 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147768026 | TCAGGCATGAAACAT[A/G]TATTTGTTAATGGAC | 79658 |
| rs150237819 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148036042 | ATCTTTACTATTCTA[A/T]TTTGTTTAATAAAGG | 79658 |
| rs150248150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147737212 | CTAGAATGCAGTGGT[A/G]CAATCTTGGCTCAGG | 79658 |
| rs150249094 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147836020 | TTGTTTTATGATTCT[C/T]ATTTTTTCCTAAGTG | 79658 |
| rs150270929 | in-del | -/TTTT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147820607 | TTTTTTTTTTTTTTT[-/TTTT]GAGACAGGGTCTCCC | 79658 |
| rs150271027 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148020486 | AGTGTGTGTTCACCC[C/T]AGGTGTCCATGGGTT | 79658 |
| rs150272022 | in-del | -/TTTT | 0.228547 | 0.249078 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148049795 | TAGATCATAAAATTG[-/TTTT]TTTTTTTTGTTTGTT | 79658 |
| rs150278390 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147794688 | TAGTTTGGGATTGTT[C/T]ATTCCCATTGCCATT | 79658 |
| rs150301876 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147913890 | AGACGTGGTGGCTCA[C/T]GCTGGTAATCCCAGC | 79658 |
| rs150306219 | snp | A/G | 6.60469e-05 | 0.00574622 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148023390 | CCGTGGCCGTCTACA[A/G]TCTTTGTCTGGAGCT | 79658 |
| rs150319865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147990260 | AACCAGTAGGTAAGC[A/G]TTTGCACAAATCTCA | 79658 |
| rs150321072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148016061 | GTGGGTTCAAATCTT[C/T]GTAAGTCAAGCACTT | 79658 |
| rs150324168 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147976125 | TTGGTCTCTGTCATT[C/T]TTTAATATATAAAGA | 79658 |
| rs150333330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147789874 | GGATGCAGATGATGT[A/G]TGGGAGTCTCATCAG | 79658 |
| rs150334217 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147899582 | TTGCTTGAATTCACT[G/T]TCATTGGAACATACA | 79658 |
| rs150348419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147749726 | CAGGATAAAATCCAA[C/T]GTAAGGATTTGACAG | 79658 |
| rs150358309 | snp | A/C | 3.30126e-05 | 0.00406266 | synonymous-codon, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148072021 | GGAACCTGGCTGGCT[A/C]GAAGGGACTCTGAAC | 79658 |
| rs150378269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148048523 | TCTTCCTTTTCCACA[A/G]TAAAAATTCTGTTTC | 79658 |
| rs150384157 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147861995 | GGGTTTCACCAGGGA[C/T]CTGTCTGTCCCTTCC | 79658 |
| rs150385702 | snp | A/T | 0.266819 | 0.249434 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147755075 | CGACAAGAGTGAAAC[A/T]CCGTCTCAAAAAAAA | 79658 |
| rs150392098 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147845763 | AGGTGCTCATGTAAG[C/T]GTGCCTTAAGTTATC | 79658 |
| rs150394779 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147929287 | TTTTCCCAAAGCTTT[A/G]GAATTATGTAAATAC | 79658 |
| rs150400795 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147814206 | AACAAGTCGTTGGTC[A/G]TTTCTTGTGGTTCAT | 79658 |
| rs150408931 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147801095 | ACAGGCGTGAGCCAC[C/T]GTGCCCAGCCTTATT | 79658 |
| rs150420132 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147898184 | CCTTAGGCTGCCTTA[A/G]GCTGCATTTCTTGTA | 79658 |
| rs150444002 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147921665 | TTGTGTCAGAAGCCA[A/G]AAGCAGTTACAATTT | 79658 |
| rs150449250 | snp | A/C | 0.0209421 | 0.100162 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147999611 | TTCGTCGTAATGGAG[A/C]TGAACACTAGTCACT | 79658 |
| rs150454065 | in-del | -/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147875360 | AGGTTAGGAGTGGCT[-/G]GTGAGCACCCTGTTC | 79658 |
| rs150461065 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147879032 | GCCTCGACCTCCCAA[A/T]GTGCTGGGATTACAG | 79658 |
| rs150461537 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147796877 | TATAACATTCTATGA[C/T]TTCTAATGTAAAAAC | 79658 |
| rs150468140 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889672 | AACATACTTTGTCTT[C/T]TTTACAAGTATCTGT | 79658 |
| rs150482099 | snp | G/T | 0.0146672 | 0.084371 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148067353 | GCTAGTTAAAAGCAG[G/T]TGCTTGCCCAGAACA | 79658 |
| rs150496853 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147815832 | GATAGTGCCACTGCA[C/T]GCTAGTCTAGGTGAC | 79658 |
| rs150501048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147930476 | CTGAAGCTGAAAAGA[C/T]AAGAAAGAACTTCTT | 79658 |
| rs150531136 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147888910 | CTTCTCTTGTCTACT[C/T]TCCTGATTCCTAGGT | 79658 |
| rs150551977 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147809545 | GAAACTAAAGCTCAG[A/G]AGCATTGTCACCTGC | 79658 |
| rs150559095 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147972759 | CAACAGTGACATTTC[-/T]CTTTTTTTTTTTTGA | 79658 |
| rs150569852 | snp | G/T | 0.0341408 | 0.126114 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148000707 | TTTTCATGTGTCTGT[G/T]GGCTGCATAAATGTC | 79658 |
| rs150578732 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148070281 | GGGATGCTGAAGCTG[C/T]TCTTTGAAGCATGAG | 79658 |
| rs150596370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147759762 | TAATTTGATTAATTT[A/G]TTTTGAGACAGGGTC | 79658 |
| rs150623025 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147996226 | ATATGGCCTATGGAA[A/G]CCTCTATCATAAACA | 79658 |
| rs150624108 | in-del | -/T | 0.99917 | 0.00481695 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147965018 | TTATTATTTTTTTTT[-/T]GGAAGAAAGCGGCAG | 79658 |
| rs150638941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147951608 | TCTTTTATTTTTCAA[C/T]TTTCTTTTCAAAACA | 79658 |
| rs150641943 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147940421 | TGTTCTTTGGCATCG[C/T]AGACTAGAGGAAGCC | 79658 |
| rs150644639 | snp | A/G | 0.0836354 | 0.186609 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148013561 | GGCATGGTGGCGGGC[A/G]CCTGTAGTCCCAGCT | 79658 |
| rs150653432 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147829234 | TTTTTTTGTATTTTT[A/G]GTAGAGACAGGGTTT | 79658 |
| rs150696625 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148008473 | TGGTGATCCCCACTG[C/G]GGGTGGTGGTACTGC | 79658 |
| rs150703898 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147906410 | TTTCAGTTTTGCAAG[A/G]TGAAAAAAGTTCTGT | 79658 |
| rs150704545 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147820890 | ACCACCACACTGGCC[A/G]TATTTTACATTTTAA | 79658 |
| rs150707598 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147780326 | TCTGCCCTACCTCTC[C/G]TCTCCTACCCAGTAT | 79658 |
| rs150709355 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147892109 | TCATTTTGCCTGGTT[C/T]CCATATCACTCTTGA | 79658 |
| rs150726109 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147967277 | GCCAGAGGACCATGA[A/G]CATCATTGAGAGTAG | 79658 |
| rs150758597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147850734 | CACCAGAAGGAACCA[A/G]TTCTGGACACAACAG | 79658 |
| rs150761428 | snp | C/T | 0.00161206 | 0.0283448 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147847159 | TCTCTAGGCATTAAG[C/T]GTAACTGAAACCCTG | 79658 |
| rs150769321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147776160 | TATCTTGTGTAGACC[C/T]GCTAGTGGCAACAGA | 79658 |
| rs150772434 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147739043 | CAAAAAAAAATTAGC[C/T]GGGTCTGGTGGCAGG | 79658 |
| rs150779794 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147961045 | TGAGCATTTATGTGC[A/G]TTTTTCCTGGTTATA | 79658 |
| rs150781196 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148038876 | TGCCTTCTCTTCAAA[G/T]AAGCAAATGTTCTTC | 79658 |
| rs150794603 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147838118 | TTGTCCCAGCTCTTG[A/G]CACCTTTGAGATTAG | 79658 |
| rs150796547 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147919294 | TTATAAATTATTCTA[C/G]TTTTGAGATAAGAAA | 79658 |
| rs150810986 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147795138 | CCTACGCTGGAGTGT[A/C]GTTACACCATCATAG | 79658 |
| rs150813807 | snp | C/T | 0.00026387 | 0.0114833 | synonymous-codon, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147955334 | TCTTCCAGAGCCTCT[C/T]ATGACCTATGAGTTA | 79658 |
| rs150831797 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148032692 | GTCCCACAATAGGCC[A/C]TCTGCAAGCTGAGGA | 79658 |
| rs150848127 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147992328 | CCCTTCACACTGAGT[C/T]ACACTGACCACCCCT | 79658 |
| rs150855740 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147978617 | TGCTTGCTTTTCCTT[C/T]GCCTTCCACCATGAT | 79658 |
| rs150856274 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148057536 | AGTGTACTAGTGCCT[A/G]CCTGTTGCATCTAGC | 79658 |
| rs150862307 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147872499 | TGCTCTGTGTATACA[G/T]TTGACCCTTGAACTA | 79658 |
| rs150863512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147791968 | TAAATAGCACTGCTG[A/G]TGAACATTCTTATAC | 79658 |
| rs150867536 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147751260 | TTTAATTGACCTGAT[A/G]TATAAGTTTAGCTAT | 79658 |
| rs150873193 | snp | A/G | 0.039522 | 0.134904 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147795929 | CAAACTCCTGACCTC[A/G]TGATCCGCCCACCTC | 79658 |
| rs150907278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147943302 | TTTCACACATAAAAC[C/T]ACAGAAAACAAGAAA | 79658 |
| rs150910721 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148050245 | AATTATTAGTGAACA[A/T]TTAATTTCTTATTTT | 79658 |
| rs150941559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148035064 | TTGCAAGAGGTAGAG[A/G]TGGTTCCTGGAGTTG | 79658 |
| rs150944938 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147994568 | TTCATATAAAGAAAC[A/G]GTTGACATCAGAAAC | 79658 |
| rs150952658 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147802557 | CTCAGCAGAGTGTCT[C/G]TACAATATAAATAGT | 79658 |
| rs150957621 | snp | A/G | 0.000227657 | 0.0106666 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147875002 | TTAACATTTATGTGT[A/G]TTTTTTAATCCATTT | 79658 |
| rs150967892 | in-del | -/C | 0.0463947 | 0.145069 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147824637 | CTGGCACCTTCTTCA[-/C]AAGGTGGCAGGATGG | 79658 |
| rs150968605 | snp | C/G/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147793500 | AAAGAATGGGGCCTT[C/G/T]AAAGGAGGAGTTGGA | 79658 |
| rs150971337 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147752625 | CTCCACCTCCTGGGC[G/T]CAAGTGATTCTTGTG | 79658 |
| rs151004924 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148020539 | AAGTGAGAACATGCG[-/T]TTTTTTGTTTTTTTT | 79658 |
| rs151014919 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147944908 | CTTTTCAGTGACTCA[A/G]CAGTGGCAATAACCT | 79658 |
| rs151024719 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147748062 | CAGCCCCAAATGTTC[A/G]TAGTGCTGAGGTTGA | 79658 |
| rs151029788 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147819099 | ATTTAATCTGTTACA[A/G]ACATTTTCAACTAAT | 79658 |
| rs151030543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148053138 | AAAAAGATTGGAAGG[C/T]GCAAAGGACATAGGA | 79658 |
| rs151043884 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147933378 | GGATTACAGGCACTC[A/G]CCACTGTGCCAGTCC | 79658 |
| rs151046533 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148006337 | CGTTAGCAGACATGA[C/T]GTGGGGAAAACGGAG | 79658 |
| rs151049944 | snp | C/T | 0.273587 | 0.248885 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147750843 | CCTGACCTCGTGATC[C/T]GCCTGCCTCAGCCTC | 79658 |
| rs151081074 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147897448 | CTTAAATCTGCCATC[G/T]TGATTTTGATTTCTA | 79658 |
| rs151104172 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147958786 | ACATTTCAATATTGA[A/G]ATAATTTAGCATTTA | 79658 |
| rs151116101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147885654 | TTGATTTGTTATTCA[C/T]GTTTGACCTCCTGAA | 79658 |
| rs151119279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147835865 | TCTCATAATAATATT[C/T]TTCCCAAGTATTTAT | 79658 |
| rs151146855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147769168 | TTTCAATGATGAGAC[A/G]TTTTCTCACTATACA | 79658 |
| rs151147300 | in-del | -/GT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147899308 | ATGAAAGCAGCTGGG[-/GT]GTGTGTGTGTGTGTG | 79658 |
| rs151158787 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148028860 | TGACTAGATGGAGAG[A/G]TCAAGGCAGATAAAG | 79658 |
| rs151163533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147843448 | CCTTTCTGCCACCTT[A/G]CCATGGATATTGCTG | 79658 |
| rs151168040 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147953471 | CTGTTTCTTCTTGAG[C/T]GAACTTTGGTAGTCT | 79658 |
| rs151170606 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147913290 | GATCAGTTATTCATT[C/T]ACTATGACAATGAGG | 79658 |
| rs151171237 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147830427 | TTGGACTTTTGACAC[A/G]GATTTTTGTTCCAAA | 79658 |
| rs151176145 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147732578 | AACGGGGAATTCATT[C/T]CGGACCAGCCCAGCT | 79658 |
| rs151187466 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147789821 | AAACAGATGGAAGTC[A/G]TTAAAAATCAGAGCA | 79658 |
| rs151189627 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148015476 | CTGAGTTTTAGTGAA[A/C]CAGAACAAACGTGAA | 79658 |
| rs151208860 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148023185 | TCCAAATCAAATGTT[A/G]TGGTGCTGGTTTACT | 79658 |
| rs151222491 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147908011 | CCATGCCCAGCTAAT[A/T]TTTGTAATTTTTAGT | 79658 |
| rs151235973 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147781733 | CCCAGGCTGGAGTGC[A/T]GTGGCGCAATCTCGG | 79658 |
| rs151238872 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147861280 | TGGACCAGGCATACT[G/T]CAGGTCGCTTCCATT | 79658 |
| rs151242926 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148009718 | ATCAATCCAGAGCCT[A/T]ATTTGGGATCTCCAT | 79658 |
| rs151245401 | snp | A/T | 0.499642 | 0.0133738 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148003023 | gggtgttaattttag[A/T]tctttcctgctttct | 79658 |
| rs151252104 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147744631 | AGCTGCAGGCTATAG[C/G]GGGTGATTGGGTGTG | 79658 |
| rs151257221 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147894015 | TTTTTAAATTGTATG[C/G]TGAAGGATACTGGAG | 79658 |
| rs151293267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147854048 | TGGTTATTTGAATTG[A/G]GGTTCTTAGGTTCTT | 79658 |
| rs151303695 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147740191 | GCACACCCTGTAGCT[A/G]GTATTATAGGTGTGT | 79658 |
| rs151308832 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147935693 | TATGAACATATATGT[A/G]TTCATAGATAAAAAG | 79658 |
| rs151309015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147963734 | AGACGTTGGGAGGGC[C/T]GTGCTCCCTCTGAAG | 79658 |
| rs151322142 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147805748 | TGAGATCAGAGTTTA[C/T]GGCAACAGTGAGCTA | 79658 |
| rs151323800 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147921202 | ATTTAGCAGTTGGTT[A/G]TATATAGAGGATAGG | 79658 |
| rs180671966 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147780211 | ACTCGTTTCACTTCC[C/G]CTTTTCTGTGGCTGT | 79658 |
| rs180675896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147738342 | GGATCACGAGGTCAG[A/G]AGATCGAGACCATCC | 79658 |
| rs180678422 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147755909 | AGGAGCAATGCATCA[A/G]TAATGAATGTAACAG | 79658 |
| rs180681596 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147798869 | TTCCTTTAGTCTCCA[A/T]GGTTTCAGATGGGAA | 79658 |
| rs180686577 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147773938 | CAGCCATTTGAGAAG[C/G]AGCACATCTGGTTAG | 79658 |
| rs180708834 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147817127 | TTTAATGAGTGACAA[C/G]AGTATATTTATTAAC | 79658 |
| rs180711609 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147746332 | TGGTCTTGATCTCTT[A/T]ACCTTGTGATCCGCC | 79658 |
| rs180713537 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147871106 | CTGGGACTACAGGTG[C/T]CCGCCACCGTGCCCG | 79658 |
| rs180720931 | snp | A/T | 0.0182019 | 0.0936463 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147762544 | TTTATTTATTTATTT[A/T]TTTTGAGACGGAGTC | 79658 |
| rs180723367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147826120 | CCTGGTGTCTGGAGG[A/G]AAAGTTCTGAGCAGA | 79658 |
| rs180732510 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147851896 | AAAGTCTTTCAGGAA[C/G]AGTTAATTCTTCCTG | 79658 |
| rs180740736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147808700 | ATGATTTGTCATAGA[A/G]TGATTTCTTGCCAAA | 79658 |
| rs180752136 | snp | A/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147788045 | TTTATCATCGGTTCC[A/T]CTCCACATCTCTTTT | 79658 |
| rs180753405 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147881649 | TTCTCAAAAGAATCA[A/G]GAGAATGACAAAAAT | 79658 |
| rs180753889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147909428 | TCTTTGTGGTATTCA[A/G]CCCCATCCTGAGATG | 79658 |
| rs180761997 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147888120 | ACTGGCTTCTTCACT[G/T]TTTGTACTTCTTTGC | 79658 |
| rs180767419 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147844222 | GTGAGTACATAATAG[A/G]TATATATATTTATGG | 79658 |
| rs180776561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147917411 | CTCCTCCACTAGGGT[C/T]GCCTGTGTCCTCCAG | 79658 |
| rs180777358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147861891 | GGCCTGGAAAAAGCA[C/T]CGTAAGTTTTCATCC | 79658 |
| rs180783301 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147990051 | GGTCCCTGACTTCCC[G/T]CAACACTCCTGATAT | 79658 |
| rs180790293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147972256 | ACATGCTTTGGGTCT[A/G]CTATAAAGGGTATTA | 79658 |
| rs180791730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147944564 | TTTAAGTAGCATGCA[C/T]GACTTAATGTGGTGG | 79658 |
| rs180795742 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147937754 | GGAGGCGGAGGCAGG[C/T]GGATCACCTGAGGTC | 79658 |
| rs180809810 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147954147 | AAATAAATGGCCTGT[A/G]TGCACTGGGAATGTG | 79658 |
| rs180811082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147902259 | ACTCTTGCCTATCTT[C/T]AGTCCATTCTCCACC | 79658 |
| rs180813985 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148034728 | TCCTCATTGTCTCAG[C/T]TGTACTGGAGGTTGT | 79658 |
| rs180815322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148016380 | TGGTGGCACGCGCCT[A/G]AAGTCCTAATTACTT | 79658 |
| rs180817334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147962580 | TCTTTTGACTTTATG[A/G]GGGGCTTATTAGGAT | 79658 |
| rs180826646 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148056373 | TGCCCTCAAATGTTT[A/G]TTTATAATTTCAGAA | 79658 |
| rs180879159 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147894232 | CTCCCATCAGCAGTG[G/T]ATGAGAGTTCTATTT | 79658 |
| rs180881614 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147866414 | ATTACAAATATTGGG[A/G]TTCTCCTGACTAAAG | 79658 |
| rs180896367 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147848048 | GTAGGGAAGGGAGTT[C/T]TTATATTTGTATTTT | 79658 |
| rs180902677 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147830178 | TTGTTTTTCTCTACC[A/C]CAGACTTTACCCTTG | 79658 |
| rs180903552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147958149 | TGGATGTCTTACTGC[A/G]TGATGTCTGTTACCT | 79658 |
| rs180907359 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147923073 | TCCATATTGGTAATA[C/T]TGTGTGTCTCAACAA | 79658 |
| rs180913350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147885530 | AGTTGAGACTTGGGT[A/G]GGGACACAGCCAAAC | 79658 |
| rs180916736 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147906358 | AATATTAGGCTTTTA[C/T]GTAGCAATTGAAAGT | 79658 |
| rs180924089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147874314 | GCTGACTCGTCACAA[C/T]TGCCTTGCTAATTCT | 79658 |
| rs180933893 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147941354 | TCTCATAAAATTCTA[C/G/T]GTGTACAGCATTGCT | 79658 |
| rs180945113 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148000953 | CCATCTGTAAATTTT[G/T]GCTTTTGTTGCCATT | 79658 |
| rs180948288 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148031379 | AAACTTAGATAATAT[A/C]CAGAACAATCCTATA | 79658 |
| rs180949448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147994177 | TTTTGAGCTTAAATG[A/G]TGCATAGTGTTTCAG | 79658 |
| rs180953363 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148013505 | CATCCTGGCTAACAC[A/G]GTGAAATGCTGTCTC | 79658 |
| rs180955992 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148021443 | TAATTTATGCTTTGG[A/T]TATACTGGCTGTGTG | 79658 |
| rs180960091 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148050577 | ACGGGGTTTCACTGC[A/G]TTAGCCAGGATGGTC | 79658 |
| rs180971762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148069836 | CCCACATTGTTACAA[C/T]CCTGAGGGCCTGTTT | 79658 |
| rs180973331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147977294 | GGGCGAGTGTGGTGG[C/T]GTATGTGTAGGTCGG | 79658 |
| rs180987597 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148060515 | TTCCCAGCCGACAAG[C/G]CTCTGAAAAATTTCC | 79658 |
| rs180995498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148005801 | GAAGCAGTGAGAGAA[A/G]TATTTACATGTGTAT | 79658 |
| rs181009563 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148039797 | TTGGCACTCTCAGTC[C/G]TTTATAATTGAGGTC | 79658 |
| rs181079348 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147997596 | AAAGATGGCCCATCA[C/G]AAGGCATCAACACAG | 79658 |
| rs181084252 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147980859 | TAGTAGTCTCTGGAG[A/T]TCTTTTCTATTTCTG | 79658 |
| rs181089045 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148008252 | TGCTGAAAGCATCTT[A/G]GATGCACTTCTTGCT | 79658 |
| rs181108169 | snp | A/C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147733345 | GGGGCGGAATTAGCC[A/C/T]CAGTGAGGAGCTGGG | 79658 |
| rs181110798 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147954447 | TGTCAATATGAAATG[A/C]CCTTCTTTATCTCTG | 79658 |
| rs181111083 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147973044 | ACAGGCATGAGCCAC[C/T]GTGACTGGCCTAATG | 79658 |
| rs181116198 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147751433 | CAGTGGCGTGATCTC[G/T]GCTCACTGCAACCTC | 79658 |
| rs181118272 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148025779 | TATAATTGTCAAAAC[G/T]ACTTGAAGGTTTCAA | 79658 |
| rs181120666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147990449 | TTCCAATTTCCAAGA[C/T]AACTAAAAGTCAGAG | 79658 |
| rs181121120 | snp | G/T | 0.0146672 | 0.084371 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148003219 | tttccatgtagttga[G/T]cggttttgagtgagt | 79658 |
| rs181122462 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148044126 | ATTGCCACTGTTTGG[C/T]AGGAAGGAAGAGAGA | 79658 |
| rs181126149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148016854 | TGCTGGAGTGGCTCA[C/T]AGAGCTCAAACACAT | 79658 |
| rs181134136 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148064188 | GTGGTTCAGTGACAG[C/G]TCCTCAGAGAGGCTC | 79658 |
| rs181140415 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148035043 | GCTGCAGATTTCCAT[A/C]GACCTTTGCAAGAGG | 79658 |
| rs181153252 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148056779 | TCTACTTAATATAGT[C/T]ATACTTTTTTCCCTT | 79658 |
| rs181180581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147767005 | AGGCGCCTGCCACCA[C/T]GCCCAGATAAGTTTT | 79658 |
| rs181238815 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147792615 | CCTGAGCTTTATTAT[G/T]CCTTATCTAGTTCTC | 79658 |
| rs181252971 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147746633 | GACCTCAGCTGATCC[A/G]CCCACCTCAGCTTCC | 79658 |
| rs181253036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147786708 | CATAGATTAGTTTTT[A/G]TGTTGGAATTTATTC | 79658 |
| rs181256346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147856865 | AGTAAAACATACTGA[C/T]TGATTGAGACAGAGT | 79658 |
| rs181257269 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147762920 | TCGCCCTTATCTACT[C/G]TGGATTCCATTTGCT | 79658 |
| rs181260962 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147777280 | TTTTTTTTTTTTTAG[A/G]CGGAGTCTCACTCTG | 79658 |
| rs181262848 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147812874 | CCATGTAATTTGTTA[C/T]AGTGAGCATTAAATG | 79658 |
| rs181264222 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147803292 | GGGATTACAGGCATG[A/T]GCCACTGCATCCAGC | 79658 |
| rs181268581 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147759893 | AGCGGGGATTACAGG[A/G]GCCTGCCACCATGCC | 79658 |
| rs181276048 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147821018 | TTACTCACTGGGCAG[C/T]TACATGTCCCTCCAA | 79658 |
| rs181281678 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147842655 | TGGAGAACACCGTCC[C/G]TCTGTTTCAGGCTGA | 79658 |
| rs181291501 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147825642 | GATCCTGTAGTCATC[A/C]ATTTTTCAGCTATTT | 79658 |
| rs181297446 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147806247 | TAAATTTGTCTAAAT[C/T]GGCTCTCCAGACATT | 79658 |
| rs181305143 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147780829 | AGTGCTGCCGGCATG[A/G]CATCCTCTGAGAGCA | 79658 |
| rs181328134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147772536 | TGTACCACAGGCCTG[C/T]GCCTTGTGGCGAGTG | 79658 |
| rs181336055 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147742178 | AAAAATGAGTGCTTT[A/C]TTTTCTGACTGTAAA | 79658 |
| rs181339301 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147839096 | TTAGATCTATCGTAT[C/G]TATCTATCTATCTAT | 79658 |
| rs181353410 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147737181 | TTGAGATGTGAGTCT[C/T]GCCCTGTTGCCTAGG | 79658 |
| rs181366745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147767194 | CAAAGAAATCTGTTC[A/G]GCTTTGTTTAAACCC | 79658 |
| rs181375240 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147783922 | AACACACATTAAATT[A/G]TGTATTATATTTATA | 79658 |
| rs181383182 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147803787 | TCTGTGGCTGAATAG[C/T]ATTCCATTATATCTA | 79658 |
| rs181410518 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147857765 | CATTATATAGAGATA[A/G]CAAAAAGTGAACAGG | 79658 |
| rs181412089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147840455 | TAGCATTCTGGTTAC[A/G]TTCCTGCTTTACCCC | 79658 |
| rs181418747 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147799211 | GGCTAATTTTTGTAT[G/T]TTTAGTAGAGACGGG | 79658 |
| rs181420348 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147834275 | GGAGTTCAAAACCAG[C/T]CTGGGCAACATAATG | 79658 |
| rs181421595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147821973 | AGGTTTGGCTTCTTT[A/G]TTTGTAAAATGGTAT | 79658 |
| rs181427340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147926974 | GTGGTATTATCCCCA[C/T]TCGCATGAGCCCCTG | 79658 |
| rs181431522 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147963932 | ATGCCAGTCATATTG[C/G]ATGAAGAAGCCCCAC | 79658 |
| rs181432165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147909944 | TTCTGTTTTACTCAA[C/T]GGGGACCTCCTCAAC | 79658 |
| rs181432594 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147895160 | GCATAGAAGTCATGG[A/G]CATTTTTTTTTTGGT | 79658 |
| rs181436378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147944983 | GCCTTGATGCTCTCA[A/G]TCGTTCTGTGAGAGC | 79658 |
| rs181438555 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147871179 | TAGCCAGGATGGTCT[C/T]GATCTCCTGATCTCG | 79658 |
| rs181442120 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147875717 | GAAGATTGCAGATGG[C/T]GATAAAAGATATTCC | 79658 |
| rs181487935 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147754766 | CATAAGTTGTACATT[A/C]TTCTGTTAGAATTAT | 79658 |
| rs181505045 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147776675 | GAGACTCTCCTATTC[C/T]CTTTGTTTCCTTGCC | 79658 |
| rs181508202 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147751636 | CCCCCTAAAGTACTG[C/G]GATTACAGGTGTGAG | 79658 |
| rs181532160 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147853160 | CATGATCCCACACTC[A/G]CTCACACAGTACTAT | 79658 |
| rs181543059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147958643 | ATGTATTCATTTCAC[A/G]GTAGATACGAATGCC | 79658 |
| rs181548664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147923679 | TCATTTGTTGCATGT[A/G]AAAGCAAATTTATCT | 79658 |
| rs181550752 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147942105 | GAAGAGGAAAAAATT[C/G]TGTGGGTCTGCCAAG | 79658 |
| rs181553620 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147994382 | AAGTTCTTGTTAATC[C/T]TTGCACAGCTGGTGT | 79658 |
| rs181556561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147817917 | ATTTAATTGCAATTC[C/T]GCACTAGAGTCATTT | 79658 |
| rs181557099 | snp | A/C/G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148030002 | CTCAGCATCCCCCCC[A/C/G/T]CCACCAACCCCAATG | 79658 |
| rs181557391 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147853378 | AGTTCTTCTCTAGAC[G/T]AGTCCAACAGTAAAC | 79658 |
| rs181559005 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147901805 | CATTCTTCCTGTCCA[A/G]CATCTGTATTTGCTG | 79658 |
| rs181560623 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147880798 | ATGAAAATATTTAAT[C/T]TAGGGTTATCGGTGT | 79658 |
| rs181561704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147978033 | GTATTCCGTGGTGTA[C/T]ATGTACCACATTTTC | 79658 |
| rs181561976 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147835521 | TGGGGTTACAGGCAT[A/G]TGCCACCATGCCTGG | 79658 |
| rs181571917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147936586 | CACCCGCCTCGGCCT[C/T]CCAAAGTGCTGGGAT | 79658 |
| rs181574567 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148006042 | AACCTGAGTAGAACT[C/T]GAGACTGTTTTGATC | 79658 |
| rs181577042 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147890022 | CACGAGACAGCATAT[A/G/T]GCACTGTTCCATTTA | 79658 |
| rs181579024 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148050304 | TTGGAAATCTCATTT[A/C]TTTCTCTGTGTTACT | 79658 |
| rs181581078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147917036 | TAGAAATGTCTCCAA[C/T]AAACATAACTCTGGT | 79658 |
| rs181581123 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147871429 | ATATGGTTTAGTTTC[C/T]ATAATCAGAAAAAAG | 79658 |
| rs181581484 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148068182 | AGTGGTTGCCTCCTC[A/C]GGGGCAGGGTTGGGA | 79658 |
| rs181583404 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147971773 | ATAGGTACTGGGGCC[A/G]CTCATAGTTTTCAAG | 79658 |
| rs181586736 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148021961 | TGCTGTCTTTGAAGT[A/T]GCTTATTTTTATTGG | 79658 |
| rs181590548 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147953609 | TGATTCTGCAGTCAC[C/G]TTTCTCATTCCTGGT | 79658 |
| rs181604020 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148002809 | TCTTTTCTCTTTTCT[A/T]CTTTATTAGTCTTGC | 79658 |
| rs181631961 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147758722 | GGTGGCTCAGGCCTG[G/T]GATCCCAGCACTTTG | 79658 |
| rs181637981 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147733519 | TCACTCACCTAGATT[A/C]TCAGTTCAGTAATTC | 79658 |
| rs181640640 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147947918 | TTCCATCCTTCTTAA[C/T]TCATTAATCTTCCTA | 79658 |
| rs181643830 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147791482 | TCTGTAGTTCTTTTT[A/T]AAAAACCTAACATAT | 79658 |
| rs181654789 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147913721 | AGGGCTTCTACATAA[G/T]AATTTTAGGGGGATA | 79658 |
| rs181669150 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147984254 | AAGCGCCCTCCCCCA[A/G]TACACATTCGCGTTC | 79658 |
| rs181682402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148026433 | ACTCCCAATTGAGAG[A/G]TGACCAGTTTAACTA | 79658 |
| rs181690095 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148045780 | AGAAATCCATCTAAG[A/G]TGTTTTTTGAGAGCA | 79658 |
| rs181694352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148012372 | TTTAAGGTGCAGGAG[C/T]GAGGTAAAGATTATG | 79658 |
| rs181701756 | snp | A/C/G/T | 0.000703478 | 0.0187428 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148064546 | CTGTTAATCCTGTCC[A/C/G/T]CAGGATTAATAAGTC | 79658 |
| rs181708563 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147907151 | ACAATTTAAAGTTTC[A/G]TCTAGTAGTTTACAG | 79658 |
| rs181710208 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148040119 | GGTCACCTAGGTGCT[A/G]GTTCAGAGCCAGGTC | 79658 |
| rs181718614 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148004577 | ATCAACCACGTGAAC[G/T]GTCTGTGGAGAGGGC | 79658 |
| rs181724705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147967124 | AACTATTTAGGACTT[C/T]TGTTGCTTTTATTCC | 79658 |
| rs181727830 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147993217 | TTATCTAGAATTCTA[A/G]AGCAGAGTCAAACCT | 79658 |
| rs181732686 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147861460 | AATGTAGTGAGCAGG[G/T]GAGGGGGAGGATCAC | 79658 |
| rs181735484 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147984597 | GAGTTCTGTGGTTAT[A/G]AATAGCATTTCTGTG | 79658 |
| rs181735628 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147740224 | CACCAGGCCTGGCTA[C/T]GTTTTGTATTTTTTG | 79658 |
| rs181745535 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147890651 | GGCCAACCTGGTGAA[A/G]CCCCATCTCTACTAA | 79658 |
| rs181756750 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147932815 | TTAAAAGTTGGAGAT[A/G]AAAAATGGAAAAAAC | 79658 |
| rs181771226 | snp | A/C | 0.00117543 | 0.0242143 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147966696 | GTTTCAAATCACTCC[A/C]AGCAGAACCTGATGA | 79658 |
| rs181774809 | snp | A/G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148000723 | GGCTGCATAAATGTC[A/G/T]TCTTTTGAGAAGTGT | 79658 |
| rs181788296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147964188 | ACGAGCCTCCTCTGC[A/G]GGCCCTTACGCTACA | 79658 |
| rs181794329 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147928457 | CTGAAAGTGCCTGCT[A/G]GTGGGGAGGCTAATC | 79658 |
| rs181799371 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148015544 | TGGTATTTTACTGTC[A/G]GACCCTGTCGTCAAT | 79658 |
| rs181814294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147998360 | TCAAAGAGCAATCAT[C/T]TATTCCCCAAAAAGC | 79658 |
| rs181823929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148055486 | TTGAGGTCAGGAGTT[C/T]GAGAGCAGCCTGGCC | 79658 |
| rs181842587 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147746002 | ACCATGTTGGTCAGG[C/T]TTATCTCGAACTCCT | 79658 |
| rs181868387 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147737853 | GAGTTGTTCCTATTT[A/G]GAGCTTCCCACCAGG | 79658 |
| rs181879539 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148061755 | TAATTTGGTTGCTCC[A/C/G]ATGTTGGCTGATGGC | 79658 |
| rs181929951 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148000766 | TTCGCCCGCTTTGTG[A/G]TGGGGTTGTTTGTTT | 79658 |
| rs181956257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148030815 | ACCTTCCTTTGTGCC[C/T]TCCTAGGCTGTATTA | 79658 |
| rs181962819 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147740951 | ATTTTGATACAGTTG[C/G]GCACATCCATAAACA | 79658 |
| rs181963436 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148068507 | TGAGAAAAAAATATC[A/G]AGTGAAAAAATAAGT | 79658 |
| rs181965883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147759397 | TAATTTAAAATTTTC[C/T]AGTAACCCCATTAAA | 79658 |
| rs181974118 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147777009 | GCTATATTCATCACT[G/T]ATCTGAGCAACCTAT | 79658 |
| rs182001386 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147829506 | GACAGTGTTTTTGAG[C/T]GAGTAGTTTTTGCTG | 79658 |
| rs182005725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147876934 | CTAGGTCATACAACT[A/G]CTAAATGCTGGAGTT | 79658 |
| rs182006105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147910311 | TACAGGCGTGAGTCA[C/T]CTTGCCTGGCCTATG | 79658 |
| rs182007029 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147895494 | TAGGCAATGTAATGA[A/G]ATAATGAGACCCTGT | 79658 |
| rs182007459 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147812275 | AAAATGGGGTACTTG[G/T]TTACATATTTATGTA | 79658 |
| rs182021119 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147933560 | TGTAGCTGTCTCAGC[A/C]CTAGAGGATGCTCTA | 79658 |
| rs182024258 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147791773 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACTGTGT | 79658 |
| rs182029398 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147948896 | GTGGGAACCCAGGAG[C/G]CGGAGCTTGCAGTGA | 79658 |
| rs182032762 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147914285 | ATACACAGAAAATTT[A/C]TGTTTCCCTCACTGA | 79658 |
| rs182034494 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147945557 | GGTTAACTGTAAATG[A/T]CTTTTTAAGTCTCTG | 79658 |
| rs182038796 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147847891 | AATGTGCAATCTGAG[C/T]TTTGAAATTACCCCA | 79658 |
| rs182058545 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147981063 | TTGGGTCTTGGTTTC[A/G]TTTAGTTCTGCTCTG | 79658 |
| rs182076381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148034317 | GCATCTCCCTCTGGC[A/G]ATTACTTATTTATTT | 79658 |
| rs182079705 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147755735 | TAGGTGATATTTTTC[C/T]ATTTGGCTCTTTTAG | 79658 |
| rs182086355 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148008371 | ACACATGCTATTAGA[A/G]ACATTTTTGTAGTTT | 79658 |
| rs182090584 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147825819 | GTACTTCCCTGGCAT[A/C]CTGAACATTGAGCGC | 79658 |
| rs182121427 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147787228 | TGACATTCTGGTAGA[A/G]GTAGTATTTATTTAT | 79658 |
| rs182127003 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147846546 | AAAAAGAAAATGTGG[C/T]TGTGGCTGGAGTTTG | 79658 |
| rs182131601 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147827782 | TAAAATTGGTTCCAA[A/G]GATTTCATAGTGGTC | 79658 |
| rs182131749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147872326 | ATGAGAACCAGGCTT[C/T]TTACTGTCTGGGAAA | 79658 |
| rs182132034 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147854354 | CAAAAATGTTCTGGC[A/G]CTGAGTAATGGCTGC | 79658 |
| rs182145324 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147946010 | CCTGTTCCCCCAGTG[A/C/T]GCGTGTGGGCCCTTA | 79658 |
| rs182150538 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911552 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCGTGT | 79658 |
| rs182156887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147929571 | CTGAGGACTAGTTAT[A/G]AATATATGTAAGGAA | 79658 |
| rs182170148 | snp | A/G | 0.000148766 | 0.00862329 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147965090 | AACTGCCAGAGAAGA[A/G]TAAAGAGATGTTGGA | 79658 |
| rs182182446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147982300 | TGGAAAGTCTGATGA[C/T]TATGTGCCTTGGACT | 79658 |
| rs182220070 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148013088 | TATAAATTTTAGAAA[C/T]AGTAATTCAGTATGA | 79658 |
| rs182226058 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147850390 | CAATAAATCTGGCTG[C/G]TGCTCACTCTTTGGG | 79658 |
| rs182242644 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148050431 | CAGGCTGGAGTGCAG[A/T]GGTGCCATCTCAGCT | 79658 |
| rs182245271 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147886856 | GCTCACCGCAACCTC[C/T]GCCTCCTGGGTTCAA | 79658 |
| rs182247582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147841266 | TTCCAAGGCTCACTA[A/G]CCAAGGCATTTTGCG | 79658 |
| rs182249975 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147866028 | CAGGTCATGGCTGAC[A/G]TTGGGAATGGAGCCT | 79658 |
| rs182256957 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147868405 | GCACACCCAGCTAAT[G/T]TTTTTTCTTTTTGGT | 79658 |
| rs182263354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147967739 | CCGCAAGGCATAACT[A/G]TGTACTGCCTGGGGG | 79658 |
| rs182267045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147942769 | CTGCCTTCCTCCATC[C/T]GGTGATGAGAGGGTA | 79658 |
| rs182267974 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147804122 | AGCATGGTACCCAAT[A/C]GGTAGTTTGTTTTTG | 79658 |
| rs182274949 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147908123 | TGCTGGGATTACAGG[C/T]ATGAGCCACCACACC | 79658 |
| rs182276051 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147985267 | GGCCTCACTGTACCA[C/T]GGTCTCTGCACAGGA | 79658 |
| rs182280050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147925108 | CTTCCTCTTCAGTGA[C/T]TTGTGGACATTTGAG | 79658 |
| rs182285663 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148003865 | TTGACTCTTTATCCT[A/C]TTTGCCCAACAGTGT | 79658 |
| rs182294059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147960588 | TACCAGTTTATTTTA[A/G]GATGAGATTTATTAT | 79658 |
| rs182296773 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147941143 | TTCCAAGATGGTGTT[A/T]TGATGATTAGAACTG | 79658 |
| rs182302104 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147823897 | GGGTTATTGAATATT[A/G]TCTGCTTTTCTTAAA | 79658 |
| rs182312248 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147904758 | ACCCAGTAATGGGAT[G/T]GCTGGGTCAAATAGT | 79658 |
| rs182313196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147805060 | GCTAGGTCCTCTATC[C/T]AGAATGGTATTTCCT | 79658 |
| rs182340637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147976104 | GTCCTATCCCTCTTC[C/T]GTAGGTTGGTCTCTG | 79658 |
| rs182367025 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147747915 | GGTTCTCAAATGGGT[G/T]ATTTTGACTGTCTAG | 79658 |
| rs182377185 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147843429 | AAATCAACTCCAGCC[C/T]AGCCCTTTCTGCCAC | 79658 |
| rs182386771 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147965235 | CACACCTGGAAGGGC[A/C]GGCTGAACGTTTGAC | 79658 |
| rs182390014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147773544 | TGTACACTTAAATAT[C/T]GTATTCTGAGTTATA | 79658 |
| rs182392877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147808188 | AGTTACAAAGGCTGT[C/T]GGAGGTGAGCCCACT | 79658 |
| rs182394011 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147946415 | TGCTTTGATCTCTAC[C/T]ACAGATTTTACGAAG | 79658 |
| rs182398280 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147982438 | GCAGTGGTGCAATCA[C/T]GGCTCACTGCAGCCT | 79658 |
| rs182405747 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148065007 | AGTCTCCAGATTCGG[G/T]TATTGACTTTGCATA | 79658 |
| rs182408020 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148009357 | GTCTGGTCTCCAACT[C/T]CTGACCTCAAGTGAT | 79658 |
| rs182412868 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147999451 | TCCACCACTGCTGTT[C/T]GCTGCCATTGCAGCC | 79658 |
| rs182414265 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148027954 | AGATATGAAAATCAG[A/T]ATTATACTGCATATC | 79658 |
| rs182425928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148046689 | TGTAAGGAAAACATT[C/T]CTCGCTGTGTATTAT | 79658 |
| rs182430150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148066558 | TGTGCGTGTACACAC[A/G]TACACATACATAGTC | 79658 |
| rs182458528 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147819153 | AAATTGGTGCATTTC[A/G]GTTTTAACTTTCCAG | 79658 |
| rs182463713 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147781596 | CTATGTTGCCATACT[A/G]AATGTTTTACTAAGA | 79658 |
| rs182520312 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147884832 | GAGATGGGGCAACGG[C/T]CTGAACTTGAAGTTT | 79658 |
| rs182523273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147883866 | GACCCGGCTAATTTT[C/T]GTATTTTCAGTACAG | 79658 |
| rs182527272 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148007071 | GTTAGCGCACTTCAA[C/G]GAGGTTAATCATCCT | 79658 |
| rs182529394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147822501 | GGAGGGAATAAACAT[C/T]TTTTCAGCATCTGTT | 79658 |
| rs182533049 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147956744 | GGAATAAGGTTTTTT[A/T]TTTTCCTTTTTTTTT | 79658 |
| rs182534061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148050974 | GTCTCAGGTCCTAAG[A/G]AATGGAGTCCAAATG | 79658 |
| rs182545590 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148070641 | ACAGAAAGGAAGGCA[C/T]TGCATGCGCGCAGTG | 79658 |
| rs182545620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148024045 | TTGCCAGATTGCCCA[A/G]TTTTTACAAAGCCTA | 79658 |
| rs182549845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148042417 | ATGCACCTGCTTTCT[A/G]CATTTGACCCTGTTC | 79658 |
| rs182558031 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148008886 | GGAGACAGAGAGTCC[A/G]CTGTCTACTGTTAAG | 79658 |
| rs182569357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148046305 | TTTAAATTCATCGTG[C/T]GGCATTACCACAAAA | 79658 |
| rs182571205 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147991817 | TTTTTCTGCACGCTG[A/G]GTACCTTTTAACTGC | 79658 |
| rs182575411 | snp | A/T | 0.0197687 | 0.0974348 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147858339 | TCTCATCCCACAAAA[A/T]TGTATTTTTTTTTCT | 79658 |
| rs182598890 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147957705 | ACCCTCCCTGCTGAG[A/G]GTTCTCAAGGTTTCT | 79658 |
| rs182602684 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147761365 | TTTAAAAATCTTTTC[G/T]AGGTTTTTCTCCTTT | 79658 |
| rs182604590 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147831941 | TGGTGACTCATTATC[A/T]TCTGTGGCCTTCCAG | 79658 |
| rs182615433 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147858995 | TTCTCATGACTCGCT[C/G]TTCTCCAAACCCTCC | 79658 |
| rs182619304 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | ARHGAP10 | GRCh38.p7 | 4:147731121 | TGATCTACCCGCCTC[C/T]GTCTCCCAAAGTGTT | 79658 |
| rs182621052 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147794908 | TCTAGGTGGTTTCCA[A/G]CATGTTATCACTCAT | 79658 |
| rs182628971 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147934273 | GCTTGAATCTAGGAG[C/T]AAGCTTGTGGCACAT | 79658 |
| rs182636228 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147896566 | TTTCATATTTTCTTG[A/G]TAAGTCTTGCCTAGA | 79658 |
| rs182646312 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147752892 | CTCATGCCTGTGTTG[C/T]CATTTTATTTTCTTC | 79658 |
| rs182652685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147768794 | CCCAGACTGGAGTGC[A/G]GTGGTGCCATCTCTG | 79658 |
| rs182658071 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147784800 | TAAAATATATATTAT[A/G]AATATAATATATTAT | 79658 |
| rs182659595 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147800838 | CTTTTTTGACACAGC[A/G]TCTTACTCTGTCACC | 79658 |
| rs182676454 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147735923 | TTTCAGTTGCTTATG[A/T]TTCATACAGGTAGAT | 79658 |
| rs182685377 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147995600 | GTAAAGACAGATTTG[A/T]CAGCCTTACAATACA | 79658 |
| rs182698486 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147764691 | AGGCGTGCACCACCA[G/T]GCCCAGCTGACTTTT | 79658 |
| rs182700501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147836149 | TGCTAGCTTTTCTTT[C/T]GTGGGAGGCAAACAC | 79658 |
| rs182701077 | snp | C/T | 0.00277738 | 0.0371615 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148023431 | AAGATGTTAATGATA[C/T]TTTTTGCTTGATAGC | 79658 |
| rs182720702 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148062885 | TAATTAGTGAACTCA[G/T]AGGGTGCTAGCAGGT | 79658 |
| rs182732036 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147760468 | TGCTTGTGGACAGAG[C/T]GGCAGATTGGGGAGA | 79658 |
| rs182764534 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147748383 | AGGGTATAGAAACTA[A/G]TAAAAAAAAGCTGAT | 79658 |
| rs182768023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147904068 | TACCATTTTGCATTG[C/T]CACCAGCAATGAATA | 79658 |
| rs182777104 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147864293 | AGGGCCGCAGATGGG[C/T]GTCCAGCCCTGGCCC | 79658 |
| rs182780264 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147765778 | GCACTCCAGCCTGGG[C/T]GACACGATGAGACCC | 79658 |
| rs182788496 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147782357 | GGTGGCATTTTCCAC[A/G]TGGCATATGCGTTTT | 79658 |
| rs182788722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147938022 | GTACCACGGACTACT[A/G]TGCAGCCCTAAAAAG | 79658 |
| rs182791641 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147826679 | CGTTTCTCCTGTGAT[C/T]CCTACTCCCCTTGAC | 79658 |
| rs182796765 | snp | C/G | 0.190205 | 0.242744 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911594 | GTCTTGATCTCCTGA[C/G]TTCGTGATCCGCCCA | 79658 |
| rs182797542 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147809372 | ATTTTTTTTCTTGAT[C/T]TTAAATTAGCTTCCT | 79658 |
| rs182805830 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147999027 | GTGTACATAGAGAGC[C/G]CTGGAAAACAAATGG | 79658 |
| rs182806936 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | ARHGAP10 | GRCh38.p7 | 4:147731518 | CGCTCTTGCCATTGT[A/C]AGGCTTCGATCTCAA | 79658 |
| rs182815485 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147862892 | ATGTGCCAACTAACT[G/T]CTGATGGCTGAACTA | 79658 |
| rs182818527 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147844731 | AAATATCTCTCAAAT[A/C]TGTCTACTTGTCTTT | 79658 |
| rs182821854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147939559 | CATTTCAATGTATCC[A/G]TGATACTTAACTAAC | 79658 |
| rs182827912 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147918204 | GCAGTGGCTTGATCT[C/T]GGCTCACTGCAAGCT | 79658 |
| rs182833452 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147801389 | AAGAGAACCATTGCT[A/G]TGCTGTAATGCTCTG | 79658 |
| rs182835728 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147974873 | AGAGAACTTGTGCAG[A/G]GAAACTCCCCTTTAT | 79658 |
| rs182846223 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147882079 | TGTTCATTATAAGCT[A/G]TTTAGTCTTGATCAC | 79658 |
| rs182848602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148027386 | GTCTTACTTGGGTAT[C/T]GTCGGGTTGGCACTT | 79658 |
| rs182849937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147902727 | GTCTGGGAGACAGAG[C/T]GAAACTCCATCTCAA | 79658 |
| rs182855878 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148037151 | TGACAAGATGCAAAA[C/T]CAAAATTTTGGACAA | 79658 |
| rs182887948 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147877479 | ATGAGTTATTTTTCC[C/T]CTCCTGGGCTTTTTT | 79658 |
| rs182889372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147778591 | GTAGTAAATATGCAC[A/G]TGTTCTCTCCCTCAT | 79658 |
| rs182892638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147815549 | CTTAAAAGAGAGAAG[A/G]GATGTGATGACAGAA | 79658 |
| rs182897226 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147841819 | AGTATTTTTAATAAA[A/G]AAGTTTTTTATAAAT | 79658 |
| rs182900866 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147785406 | GTGCCTTGAGAACTT[C/T]AGGCATAAGTGAAAG | 79658 |
| rs182901929 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147818330 | CATCACTTTGGGAGG[C/T]CGAGGCAGGTGGATC | 79658 |
| rs182920634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147915061 | TTGGATGCCTTAGTG[A/G]GGTGAAGTACTGCCT | 79658 |
| rs182929292 | snp | G/T | 0.0345262 | 0.126772 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147824232 | GAGGCTGAGGCAAGA[G/T]AATTGCTTGAATCTG | 79658 |
| rs182935625 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147805588 | TTAACAATATTGATT[C/T]GTCATATCCCTTCTC | 79658 |
| rs182941790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147949648 | GAAAGAGTAGGTAAG[A/G]GATATAAACATATAA | 79658 |
| rs182949023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147878241 | GCTGGGACTACAGGC[A/G]CGTGCCACCACGCCT | 79658 |
| rs182949537 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147978849 | TATGTTTTTTGGCCA[G/T]TTGTCCGTCTTCTTT | 79658 |
| rs182950671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147860015 | GATATTCATTACTTT[C/T]GGCAGTGGTTAATGT | 79658 |
| rs182965310 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147842148 | ACCATATTGACCAGC[C/T]GGTCTCAAACTCCTG | 79658 |
| rs182973954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147915511 | AATAGATGCAGATCT[A/G]TCTAGAAGGCTTTCT | 79658 |
| rs182987147 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148006982 | TACTACCTGGATAGC[G/T]TTTCTTGATTTACAT | 79658 |
| rs182998666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148041338 | AGGGAAGGGATTTCA[A/G]GGGGGAACTATCTCT | 79658 |
| rs183026391 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148047813 | ATTTATAATTCATCC[A/G]GAGAATCTTTTTTTT | 79658 |
| rs183029376 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148066866 | TTGCTATAGACGTAT[G/T]GGGGAGAGGCTGCTG | 79658 |
| rs183065867 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147930333 | TTATTTCCGTATTTC[C/T]CTTACTGATTAATCA | 79658 |
| rs183082183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147903504 | CATTAGGGCTCACTC[C/T]TGGATTGTACATTTT | 79658 |
| rs183082433 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147918924 | AATTATTGGGACCTT[A/G]CTCTCTCATACTTAC | 79658 |
| rs183101670 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147955110 | TAGGGATTTGTGGCT[C/T]CCTAGGCTTTGATAG | 79658 |
| rs183110778 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147973569 | TTTAGTTATTTTTAA[A/G]TGTGTAAGAAATTAT | 79658 |
| rs183116210 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147938400 | GTAACTATAATTTTT[A/T]AAAAAAGCAAAGAGA | 79658 |
| rs183122343 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147990883 | GGGCCTGGTGTTGTG[G/T]TGCATACCTGTGGTC | 79658 |
| rs183128693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147738864 | CCAAATTTTGATTGT[A/G]GTTCGGGATGCTGGA | 79658 |
| rs183143079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148003605 | GTGCTCCTGTATTGG[A/G]TGCATATATGTTTAG | 79658 |
| rs183148287 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148017764 | ACTTAAGTATTTATT[A/T]ATTCAGTTCAATCAA | 79658 |
| rs183156900 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147836793 | ATAAAATACCATACT[G/T]GGATTTGTTGGGAAG | 79658 |
| rs183196837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147764385 | AGCACCTGAAGACCA[A/G]GCACACCTAACACTA | 79658 |
| rs183202709 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147781115 | TGTAATACCAGCATT[G/T]CGGGAGGCTGAGGCG | 79658 |
| rs183212272 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147872605 | GCCTACTGTTGATCA[C/G]AAGCCTCACCCATAA | 79658 |
| rs183212433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147800442 | TATGTCGAGGCTCCC[C/T]TAGTTATTGTTGGTG | 79658 |
| rs183212776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147756708 | GTTTACAGTGCTATT[C/T]ATGGTTTTAGGCATT | 79658 |
| rs183216788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147915940 | ATGACCCTGTCTGTA[C/T]AAAAATTTTTTTAAA | 79658 |
| rs183223838 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147898499 | TCCATTGAGGTTCTT[A/G]GATGTGTAGGTTTGA | 79658 |
| rs183229160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147951615 | TTTTTCAATTTTCTT[C/T]TCAAAACATTAAAAA | 79658 |
| rs183250069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148006398 | CGTCAAATATATGAC[C/T]CTTGTCAGCCTGTTC | 79658 |
| rs183250098 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147970117 | CCCACTCCTGGCTCT[C/T]TGTTCCTGCTCAGTT | 79658 |
| rs183252818 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147936227 | TTTTTCCTGTATCGG[G/T]CTCAAAAGGTCTCTG | 79658 |
| rs183257688 | snp | A/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148023284 | CGGACGCCGCCCGAT[A/G]CTACATTCCCTGAGC | 79658 |
| rs183263853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147986178 | CATTATCAGTTTCCT[C/T]ATCTATGAAATAAGA | 79658 |
| rs183266943 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148040622 | GCTGGGATTACAGAC[A/T]TGAGCTGCAGCGCCT | 79658 |
| rs183269794 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148001395 | TTGTCTTGGCAATGC[A/G]GGCCCTTTTTTGGTT | 79658 |
| rs183269829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148062371 | CTTAGGTGAAGAGCA[C/T]CTGGGTGCTGCAGAC | 79658 |
| rs183283455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148032490 | AACTGCTGTAGGTAT[A/G]TGCCAAACATGATTG | 79658 |
| rs183292419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147813243 | TCACTGGCCTATACC[C/T]GAGTTGTCACTCATG | 79658 |
| rs183301156 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148063376 | CCTGAGCAGGTTCTT[G/T]TGTTCTCTGCTGGCA | 79658 |
| rs183313052 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147777676 | ACCTTTAAGGGTGAC[C/T]CATGTCTGTGTCATT | 79658 |
| rs183314742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147848571 | TTTAAGCTCTTTAAA[A/G]CTTGTTGCATTTTGG | 79658 |
| rs183316066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147753442 | TCTGCCTCCTGGGTT[C/T]AAGCGATTCTCCTGC | 79658 |
| rs183349054 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147886166 | ATATTCTAAAATCCA[A/G]AAAAAATTGAAATCC | 79658 |
| rs183376489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147788546 | GTGAGATTAGGGGTG[A/G]GACCAAGGGTAAGGA | 79658 |
| rs183377025 | snp | A/G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147760963 | TCAACTGAGAACTGT[A/G/T]AAAGAGCTGGTTGTA | 79658 |
| rs183379728 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148018137 | CTTATGTTGTAAATA[C/G]GTAGGTGCTGTGAAG | 79658 |
| rs183384375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147778024 | TGAGGATCCAGACAA[A/G]TCTTGCTTTCTGCCT | 79658 |
| rs183386658 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148036158 | ATATGATATAATTCC[A/G]TGACCTAGGTTTTAT | 79658 |
| rs183388862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148058812 | GGCCCCACTGCTGCA[C/T]GTGAAAGCTACAAGG | 79658 |
| rs183405744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147950285 | TAAATTTTGGTGATG[C/T]ATCAAATGGGATAAA | 79658 |
| rs183406760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147743205 | TGCCTGGCTATTTTT[A/G]TGTATTTTTAGTGGA | 79658 |
| rs183413222 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147756490 | TAGTCCCCCTTATCC[A/G]TGGTTTCAGTTACCC | 79658 |
| rs183417908 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147849441 | TTCCTCTGATTAAAT[C/G]TGCTTACATGGGATA | 79658 |
| rs183421105 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147985930 | ACTCACTTTTACCAG[C/T]CAGATGCCATCATGG | 79658 |
| rs183427184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147819347 | TAAACAAACATGTTC[A/G]TATATATTATGTGTA | 79658 |
| rs183427659 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147831657 | GAACTGACCTTTACA[A/C]TTGGACAGCATTGCT | 79658 |
| rs183431032 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148013760 | TCCAAAAGAAAAATA[A/G]CATTCACGTTGGAAA | 79658 |
| rs183433872 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147813782 | CGTAATTGTATTCTC[A/G]TTATTTAAGGCTTTG | 79658 |
| rs183446063 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147891624 | TGTGACTTACATCTC[A/C]ATAGAGCTATTTTAA | 79658 |
| rs183452277 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147867283 | TTTTCCTTTGGAAAA[C/T]GTGTGCTTTCTGCCA | 79658 |
| rs183456185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147854959 | TTTTCATAGCCTTCT[A/G]TTGCTGAGTGTGCTG | 79658 |
| rs183458781 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147863696 | GTGCCTGTTAACTGC[G/T]GGTGGCTGAACTATT | 79658 |
| rs183469735 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147789098 | TCTTAGCGTCTCCCA[C/G]TGTCTTTGGGAGTGA | 79658 |
| rs183480936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147827649 | CTGAGAACTTTGAAA[A/G]ACTCTTGTTTTACTT | 79658 |
| rs183495799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147733216 | TAAACTCGGAAGAAG[A/G]CACGAGATACAGGAG | 79658 |
| rs183505643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147775954 | AACTGAGGCATAGAA[A/G]AGTTCCGTAAGCTGG | 79658 |
| rs183510378 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147790300 | GTGACCTCATCTAAA[C/G]TTAATCAACTCCCAG | 79658 |
| rs183524030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147930999 | GTGTTTTCTGGAGCT[A/G]TGTGGTCTCTGGCTC | 79658 |
| rs183528462 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147739848 | TCAAGCGATTCTCCC[A/G]CCTCAGCCTCCCAAG | 79658 |
| rs183550125 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147736497 | TTTTTTGTAAAATGG[A/G]ACTGATACAGAAAGC | 79658 |
| rs183551662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147866536 | TCATTTTCTATAAAG[A/G]CCAATTAATAGATAA | 79658 |
| rs183557594 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147793141 | TGAGACTCTCTGGAA[A/G]AAAAGAAAATGTGTG | 79658 |
| rs183559258 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147830985 | CACTTGTCATCAAAG[G/T]ATGGTCCCTGGTCCA | 79658 |
| rs183562695 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147770155 | TATGAATGTTGTAAT[A/T]GGAGAATCTGCCTCA | 79658 |
| rs183563855 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147965985 | CTTTTTGAAGATGGT[A/G]TCTTTGAATTGAGAC | 79658 |
| rs183567199 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147810093 | GCTTATTTACATTCA[C/T]CCTTTTTGAGCGGGA | 79658 |
| rs183579767 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148058722 | ATGGACTGCTGATCT[C/G]TTCCATTTTCTAAAA | 79658 |
| rs183581603 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148029086 | AAAATGGTGTAGAAT[C/G]TCTTGGTATAAATAG | 79658 |
| rs183598808 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147935159 | TGATGGTCGAGCTGT[C/T]TGTTGTGATTAAGTT | 79658 |
| rs183625817 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147772315 | GGTAGTGTGTATCTG[A/C]CAGTTGACACTTTAC | 79658 |
| rs183632083 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147786481 | AGGATTTTCTTTTTC[C/T]GCTTTTTCATTGATC | 79658 |
| rs183637993 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147969894 | TAATTAAGTGCTCTC[A/C]GGCTTTCTATTCAGA | 79658 |
| rs183641117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147806217 | GCGGCTTTCCAGGTC[A/G]GATCAAATTTACTCT | 79658 |
| rs183641764 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148001146 | ATGGCTAGCCAGTTT[A/T]CCCAGCACCTTTTAT | 79658 |
| rs183642239 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147942375 | TAGAATTTTTTATTG[A/C]CATTTTTACACAAAG | 79658 |
| rs183654227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147736967 | TGCCTGGGACTGCTA[C/T]CCACTATCTTGGGCC | 79658 |
| rs183657609 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147878393 | AGCCACTGCGCCTGG[C/T]CCATACTTCATTTTT | 79658 |
| rs183659440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147754327 | GCTATTGTAGTTCCT[C/T]TTGCAAATTCCTGCT | 79658 |
| rs183664819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147842482 | CTTTCTGAGCATTTC[C/T]TGGGTCCCATTCTGA | 79658 |
| rs183668466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147978371 | AATCGCCATTCTGAC[C/T]GGTGTGAGATGGTGA | 79658 |
| rs183673517 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147825363 | GAGGCAGGAGAATCA[C/G]TTGAGCCCGGGAGGC | 79658 |
| rs183687127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147809704 | GTTCCATGGAAGACA[A/G]TTTTTCCATGGATTG | 79658 |
| rs183703944 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147775743 | TCCCTAGGCATGGGG[C/G]CTCTAAATCCTTTTG | 79658 |
| rs183710063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147844926 | CTTGAAAACCCTCCT[A/G]TGGCTTTCCACTGTA | 79658 |
| rs183737175 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147883106 | CACTTTGTAATAAAT[G/T]AATTGAAGACCATTT | 79658 |
| rs183738136 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148032882 | TTGGGAGAAAGATGA[C/T]GGCTGTGGAAGATTC | 79658 |
| rs183752095 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148071572 | AGTGAGCCGAGATCG[C/T]GCCACCGCACTCCAG | 79658 |
| rs183755068 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147873936 | GCGAGAGGGAACCTA[A/G]CCGTCAACAACTGAG | 79658 |
| rs183757513 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147893810 | TTTAACAGAATTTTA[G/T]TGGAACTGATAGAAC | 79658 |
| rs183770060 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147931858 | AAGAGCTTCTGCACA[A/G]CAAAAGAAACTATCA | 79658 |
| rs183772246 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147966235 | AAGCAAGATTAGCAC[A/G]TACAGTTGGCTCTTT | 79658 |
| rs183774266 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147947664 | TCCTTTGGCCTCCCA[A/G]AGTCCTGGGATTACA | 79658 |
| rs183779479 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147982921 | AGGGTCTTACTCTCG[C/T]CCAGGCTGGAGTGCA | 79658 |
| rs183782565 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147946972 | TTTTAGGAATTAAAC[A/G]CTATGAAACAACTCG | 79658 |
| rs183800279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148035961 | TTCTTTTTTAAAAAA[A/G]ATATCTCTAGGTTCA | 79658 |
| rs183805912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147884274 | GGAACCACTCTCCAC[C/T]CCTCAAAGACATTGA | 79658 |
| rs183808893 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148009630 | AGAAATTAATTCACA[A/T]GTTTCTAGTGAACTT | 79658 |
| rs183809766 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147904432 | GTTCCCCTTCCTGTG[C/T]CCATGTGTTCTCATT | 79658 |
| rs183818864 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147821584 | AGAAACTTACAGTGG[G/T]GAATGTTGAACAAAA | 79658 |
| rs183821533 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147864749 | AATCAGGCAGCACAC[C/T]GTATTTTGGCCCATG | 79658 |
| rs183828300 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147940226 | GTCCAGAATTGTGAC[A/G]GTACATTTGGTTGGA | 79658 |
| rs183834042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147957031 | AGTGGTGAAAACGAT[C/T]GCAGAAACGCAGACA | 79658 |
| rs183843898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147921406 | TCTCTCTGCTTTAGA[C/T]GATGAGAGATCCAAT | 79658 |
| rs183847028 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARHGAP10 | GRCh38.p7 | 4:147730479 | CTGCTGGTTTTAGTA[A/G]GAACTGAAGCTTTCA | 79658 |
| rs183865749 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147959727 | GTTGCATAGTATTTC[A/T]TGGTGTGTATGTGCC | 79658 |
| rs183866915 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147871109 | GGACTACAGGTGCCC[A/G]CCACCGTGCCCGGCT | 79658 |
| rs183888240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147909524 | TTGTTATGAATAACA[A/G]AAGATGTTCTTATTA | 79658 |
| rs183892446 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147926899 | TCAAACTAGATAATA[A/G]CGAGGTTGTACTTGT | 79658 |
| rs183903182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147888957 | GAATTATAAGAAATT[C/T]GTTCCTTGTCTATTA | 79658 |
| rs183903594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147986536 | CTCCTCTCCCCTGGT[C/T]ACCTACCCTCTCCTC | 79658 |
| rs183905733 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147994505 | TTGGATTAATAGGTT[A/G]TGGGGAAGATTTATA | 79658 |
| rs183919003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148014123 | TGTGTATGGACTATA[C/T]CTTATAGTTGACATA | 79658 |
| rs183922403 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148002249 | GAACCAGCCTTGCAT[C/G]CCAGGGATGAAGTCC | 79658 |
| rs183926784 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147962891 | GTCTTGAACTCCTGA[C/T]CTCAAGGGATCTGCC | 79658 |
| rs183926981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147944592 | TGGTACCATTTTGAC[A/G]GGTTTTTCTTTTTAG | 79658 |
| rs183934737 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148033655 | GTTTACAAATGTTTC[A/T]GCTTAACTCCGAAGC | 79658 |
| rs183936029 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148014685 | AGGTAGTTCTGGAAT[A/G]TGTTGTACTTTATAA | 79658 |
| rs183938790 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147980660 | CTGTGAATCCATCTC[A/G]TCCAGGGCTTTTCTT | 79658 |
| rs183944275 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148052102 | ATTTGCCTAAAGTTC[A/G]GAAAAATAATCATTT | 79658 |
| rs183948361 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147735311 | AAAGGATATAGACAC[A/G]TACCTGTGACAAGGT | 79658 |
| rs183953839 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148052263 | CTCCTTCAGAGAGGG[A/C]TTCCTCAACCCCAGC | 79658 |
| rs183954044 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148072252 | TGGGCAGGGATGGGA[C/T]GCACCACACAGAACT | 79658 |
| rs184038388 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147768426 | TCTAAAGATTCCGCT[G/T]TTAACATCAGCTTAA | 79658 |
| rs184044190 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147983691 | GCTATGTCATCTTTT[G/T]AATCTTGAGTCGTTT | 79658 |
| rs184067729 | snp | A/T | 0.0696718 | 0.173152 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148000415 | CTTTATAGCAGCATG[A/T]TTTATAATCCTTTGT | 79658 |
| rs184073651 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148029956 | GGATGCCTCCCCTGC[A/G]TTGGTGTCTCCCCAG | 79658 |
| rs184078630 | snp | C/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148011939 | CCCCCAGTAACTAAA[C/T]GCGTAAGAATAACAG | 79658 |
| rs184081986 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148049910 | TCTCACTCTGTCACC[C/T]AGGCTGGAGTGTGGT | 79658 |
| rs184084441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147907444 | CTCTAAATAAACTGC[C/T]ATTGCAGGTGCCAGG | 79658 |
| rs184096184 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148067601 | TTTTCCTGTGTTCAC[A/T]TATCCATTTGGAGTC | 79658 |
| rs184146488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147803387 | TGATACATGCATACA[A/G]TGTGTAATGATCAAA | 79658 |
| rs184149875 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147829044 | CCACCATGCCTGGCT[A/G]ATTTTTTTGTATTTT | 79658 |
| rs184172544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147751219 | AATGAGTAGATCACT[A/G]TTGTTTTAGATTAGA | 79658 |
| rs184179111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147752303 | TGCAAAGCTTACTTT[C/T]GGGAAATTAAAAATT | 79658 |
| rs184214305 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147820442 | AGGCAACCGCCACCA[C/T]GCCCGGCTAATTTTT | 79658 |
| rs184233084 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | ARHGAP10 | GRCh38.p7 | 4:148072977 | TCTGATGTGTGCAAT[C/T]CTGGAAGGGCATTCA | 79658 |
| rs184243666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147886801 | TTTGAGATAGAGTCT[C/T]GCTCTGTCACCCAGG | 79658 |
| rs184260486 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147856361 | ACGTATTTTAAATAG[C/T]GTTACAGAAATCACT | 79658 |
| rs184270360 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147831058 | CACCCCAGAACTCTA[C/T]TGAGTCAGAAACTCT | 79658 |
| rs184273268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147842944 | TCTCTAAGAAGTGTT[A/G]TCTCATTTGTAATGA | 79658 |
| rs184283366 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147825652 | TCATCAATTTTTCAG[C/G]TATTTAGGAAAGACT | 79658 |
| rs184295975 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147880334 | TGCCTTTCCCTGAAA[A/C]ATATTTAAAGCAGCT | 79658 |
| rs184298255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147943172 | CTACTTTAGTTTAAA[A/G]CATCAGAGTGGAAGA | 79658 |
| rs184298527 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147901068 | TTGTTTCAAAAACTA[C/T]AGAATTTTTATATTT | 79658 |
| rs184308181 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147861256 | ACTGGCTCCGTGCAA[A/G]GCTGTGGCTGGACCA | 79658 |
| rs184323718 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147766886 | GTCTTGCTCTGTCGC[C/T]CAGGCTGGAGTGAGT | 79658 |
| rs184324632 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147916844 | GGAAGCCAAGTTCTG[A/T]AGACAGTGGAATTGC | 79658 |
| rs184324964 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147922935 | TACTGTTTACTCAGA[C/G]AAAATGTCTTATTTA | 79658 |
| rs184328866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147961359 | GTGAAATTCCTGCCC[C/T]GGTCTTTTGCCCTTT | 79658 |
| rs184329071 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147979244 | ATATGATGAGAGGTA[A/G]TAGTCTAGTTTCATT | 79658 |
| rs184354365 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148068183 | GTGGTTGCCTCCTCA[G/T]GGGCAGGGTTGGGAG | 79658 |
| rs184366722 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147803045 | ATGGAGCCTTGCTCT[A/G]TTGCCCAGGCTGGAG | 79658 |
| rs184393205 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147745636 | AGCTGGGACTACAGG[C/T]GCCCACAACCACGCC | 79658 |
| rs184396826 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147761820 | AGGTGATTTTAAAGA[C/T]GGCATTACTAGGAAA | 79658 |
| rs184401173 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147860852 | ACTAGTGATTTGCTT[G/T]GAGTAGTAAAACGTA | 79658 |
| rs184408376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147778785 | ATCCTCTTGCTCCAT[C/T]TCATTTTAATAAGTG | 79658 |
| rs184415713 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147838531 | GGGATATGTTTCCAT[G/T]ATTTCTCTTCCTCCT | 79658 |
| rs184425601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147899462 | AGTTTTTGAAAAACA[A/G]TGGTTTCATAGGTTC | 79658 |
| rs184430632 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147941077 | GAAGAATTTAATGGG[A/T]GTACAGCATCTGCTT | 79658 |
| rs184444036 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147921766 | CGTTTTACCTCCAGT[C/G]CCTCCCACCTGCCGT | 79658 |
| rs184459787 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147992855 | GGGACTTTCTACTTA[A/G]ATAATGAAAGACACC | 79658 |
| rs184462400 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147957245 | GATTTAATGAGAAAA[A/C]GTACATGTACTAAAT | 79658 |
| rs184462792 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147796282 | TTAATCCTTGCCCTT[A/G]GGGAATATATAATCT | 79658 |
| rs184465692 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147975764 | ACTATTACATTGAGG[A/T]TTATGTTTTCAACAT | 79658 |
| rs184474810 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148004431 | CCTAAGATGACCTCC[A/G]GTGACCCAGGCCCTT | 79658 |
| rs184485724 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148038988 | TTAAACTATATTTCT[C/T]TCCCCACTTCCAATA | 79658 |
| rs184485966 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148020015 | GCATTATGTGTAATA[G/T]TTGAGTATCCCACAT | 79658 |
| rs184487132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147970954 | AAGAATTAGCCAGGC[A/G]TGGTGGCGGGCACCT | 79658 |
| rs184506682 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147997148 | CCTGGTGTAGTGGTG[G/T]GAATAAAAAGTGTTA | 79658 |
| rs184532867 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148025008 | TTGGTCTTAGGATCA[C/T]GTCTACTATTTTGAT | 79658 |
| rs184537889 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, downstream-variant-500B | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147783093 | TGTGTTAAATTATAT[A/G]TTATGTAAATTATAT | 79658 |
| rs184546586 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147758776 | TTGAGGTCAGGAGTT[C/T]GAGACCAGCGTGGCC | 79658 |
| rs184547291 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148064031 | GCCGCCTCCTTCTGC[C/T]GGCTGGCCGTGTGTC | 79658 |
| rs184550853 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147776723 | TGCTGCTTCTGTTGG[A/G]TGAAGGTTTGATAGG | 79658 |
| rs184558852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147839296 | CCCTTTAGTTTAATG[A/G]AATGGGAAGTATCTG | 79658 |
| rs184562026 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147820246 | TCTTAGAGAACAATT[G/T]CATGTTTGCCTGGTT | 79658 |
| rs184562421 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147852785 | GTAGAATGGCATGAT[C/T]TTGGCTCACTACAAT | 79658 |
| rs184568841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147879103 | ACTAGCAGTATTGCT[A/G]ATTTGTTTCATTGAT | 79658 |
| rs184570373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147802098 | TCGGAGGAGTGGGGC[A/G]TATGAGGATGGACTG | 79658 |
| rs184576955 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147740243 | TTGTATTTTTTGTAG[A/C]GATGGAGTTTCACCA | 79658 |
| rs184581453 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147912580 | ATATATATATATATA[G/T]ATATATATATATATA | 79658 |
| rs184583300 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147873504 | ATGACCAAGGAGGGG[A/C]ATAAAGTCAGGGTGA | 79658 |
| rs184584490 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147952374 | CTTTACATCCTCACC[A/G]ACAATATACAAAGGT | 79658 |
| rs184588261 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147972178 | GGTAGAAAGTATAAC[A/G]TAAGGTATAGTTAAA | 79658 |
| rs184596637 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147874378 | GCCGTTTGACAGATA[C/T]TGGCACACCAAGTGT | 79658 |
| rs184599047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147947796 | ATCAACTTATATGAC[A/G]TATTTTGTATTTTTA | 79658 |
| rs184600152 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147988743 | GCCTTTTAGTGTTGA[C/G]TTTTCCCCCACACTT | 79658 |
| rs184601096 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147975386 | AGACAGAGCAGTAGG[C/G]AGAAGGGCATATGTG | 79658 |
| rs184601220 | snp | A/C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147855422 | GAGAGTAACTATGTA[A/C/G]TATCAATACATTGGA | 79658 |
| rs184601748 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148024611 | CATATGATACAAATA[C/T]TAGTTTTACAATTGG | 79658 |
| rs184602756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147837872 | ACTGATGTTCCTGTA[C/T]GTGCCTGATTGTAAG | 79658 |
| rs184610884 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148042694 | GTCTTTGCCTGTCTT[C/T]TGCATTATACTCTGG | 79658 |
| rs184615317 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148016116 | GTACCCAAAAGTTGC[A/G]ACTGTTATTATTTGA | 79658 |
| rs184621735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147892343 | AGCCCATGCAATTTG[A/G]CTGAATATGAGAATG | 79658 |
| rs184622874 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148002828 | TATTAGTCTTGCTAG[C/T]GGTCTATCAATTTTG | 79658 |
| rs184627882 | snp | A/C/T | 0.00279258 | 0.0372817 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148063840 | CGTCCTTTCCATGAA[A/C/T]GGACACAGAGGTTGC | 79658 |
| rs184631684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148003947 | GAAAGCTGCAAAATT[A/G]TGCTAAGAGACGTGA | 79658 |
| rs184655509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148007667 | TGCTCAAGCATTGTG[C/T]AACTTCAGCAATTCG | 79658 |
| rs184666948 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148043768 | TGTATATATATGTGT[A/G]TATATATGTATATAT | 79658 |
| rs184683591 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147857095 | GACCTCAGGTGATCC[G/T]CCCGTCTTGGCCTCC | 79658 |
| rs184713817 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147894691 | ACTCATGAAGATTTT[G/T]GGGGTATATATGGTG | 79658 |
| rs184733467 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147870433 | CATAAATATTTTGGT[C/T]ATCTTTTAAGTATTT | 79658 |
| rs184737637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147851457 | GGCTCAATTGATCCT[C/T]CTGCCTCGGCCTTCC | 79658 |
| rs184740247 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147833494 | TTACCCAGTCTCAAG[C/T]AGTAACTTCATAGCA | 79658 |
| rs184741486 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148020790 | AACAGAATGATTTGC[A/G]TTCCTTTGGGTATAT | 79658 |
| rs184746900 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147966578 | GGGTGGTTAAGTCTC[C/T]TGACCCCTTGCTTTT | 79658 |
| rs184753359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147992390 | ATTTTTCTCTAAAAA[A/G]CGTTTTATTTTGTAT | 79658 |
| rs184755020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147932439 | GATAAAGAAAATGCC[A/G]TACATGTAATATACC | 79658 |
| rs184755586 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148039239 | TCAGTATAGTTCTTC[A/G]TGTGGCCATCCTTTG | 79658 |
| rs184759568 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148060462 | TGTGAACCCATTACA[C/G]GACTTAAGTATATTT | 79658 |
| rs184760008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147887589 | TTTCCTGGCCAGGTG[C/T]GGTGGCTCATGCCTG | 79658 |
| rs184767724 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148018521 | AAACAGTGTCCCTTT[A/G]AGTCATTCCTGGTGT | 79658 |
| rs184793047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147987930 | TTCCTTTTAATAAAT[C/T]CACTTTTACTTATGC | 79658 |
| rs184794932 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148015108 | GTAGAGAGGGCCTCA[A/T]ACTGATAGGTAGCAG | 79658 |
| rs184798891 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147736672 | GACTCAGGGGAAGGC[A/C]TTTCAGGGTAATTCT | 79658 |
| rs184819330 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148053861 | GGCCTAATTCGTGCC[C/T]TCCTTTGCTGTGCTG | 79658 |
| rs184855825 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147744920 | GAATACCGAGGCTGC[C/T]GAGAGAGAATGTAGA | 79658 |
| rs184884718 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148034909 | TTTAGTCTTTAAACA[A/G]TGCCCCAGGACTGTG | 79658 |
| rs184886848 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148056554 | CTCTTCACTTCCCGC[C/T]CCCACCCCACCTCCG | 79658 |
| rs184891620 | snp | A/G | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147971271 | TAAGTTCTGTTCTTA[A/G]CAGAGTATACTTGTT | 79658 |
| rs184900104 | snp | A/G | 0.0032219 | 0.0400071 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148002648 | TAGTCTTGGGAGGGT[A/G]TATGTGTCAAGGAAT | 79658 |
| rs184900727 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147740075 | TTTTTTTGAGACAGA[G/T]TCTTGCTCTGTTGCC | 79658 |
| rs184917479 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148000277 | TTTTTGATGGCTGCA[C/T]AGTATTCCATGGTGT | 79658 |
| rs184924825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148033804 | AGACTTCATTGGCAC[C/T]AACTGAGAATGACTG | 79658 |
| rs184925396 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147983368 | TTTTTTGTATTTTTA[A/G]TAGAGACAGGGTTTC | 79658 |
| rs184960125 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147776365 | GCTGGAATTACAGGA[A/G]CGCGTCACCACACCC | 79658 |
| rs184968574 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147810323 | TTACTAGTGATTTCT[A/G]TTTATTTTGTGAATT | 79658 |
| rs185058937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147758498 | AAGAAAGCCTGTCCC[C/T]TTTTGGCTAATACTT | 79658 |
| rs185061710 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147895994 | AATGATCATTAAATA[C/T]GTTTCTTTAATCTTT | 79658 |
| rs185071032 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147798303 | GCTGTGTTACTTATA[C/T]AACACCTGCTATTAT | 79658 |
| rs185081544 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147790664 | AAAACCTGAGCTAGA[C/G]TAGCCCACATTTGGT | 79658 |
| rs185084758 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147816071 | TTTCTTTAAACAGAG[G/T]AATCTGTGGCCAAAG | 79658 |
| rs185097258 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147816917 | CCCTGTTCCTCTTTA[G/T]ATAAAACATGAAAGA | 79658 |
| rs185099952 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147754955 | CAAAAATTAGCGGAC[A/G]CCTATAGTCCCAGCT | 79658 |
| rs185104085 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147887226 | AGACACCCACCTCCA[C/T]CCTCAGTGCCCAGAC | 79658 |
| rs185107832 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147762352 | ATGCCACAAATTAAT[C/G]TTATTTCTAACTGGT | 79658 |
| rs185111964 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147779933 | TAGACACTTACACCC[C/T]TATAGTCTTGCCCGA | 79658 |
| rs185113925 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147786811 | TTACAGAAATGAGTC[C/T]GTATTCAGCCTGTGC | 79658 |
| rs185118116 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147850690 | GAGGGTCCGCGGCTT[C/T]GTTCTTGAATTCAGT | 79658 |
| rs185120023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147925610 | TCTTACAGGGAAGGT[A/G]TTAGAGGAAAAAATA | 79658 |
| rs185153397 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147953142 | TGATATATTATTTTA[C/T]TTATCTTGTGGAATT | 79658 |
| rs185189479 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147832890 | TGAAACGGACATGAG[A/G]TTACTTCTCTTTTAC | 79658 |
| rs185202665 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147732785 | CCTAGGCACTCCTGG[C/T]CCGGAGTCAGGTTTC | 79658 |
| rs185212360 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147766205 | TGAGGCAGGAGAATC[A/G]CTTGACCCTGGGAGG | 79658 |
| rs185215415 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147869558 | ATCATTTTCTGTAGA[A/G]AAATGGGGAAATGAC | 79658 |
| rs185216241 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147752364 | CTATTAAAAGTTATA[C/G]GAAAGGAAGTCATTT | 79658 |
| rs185220364 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147792219 | AAACTTTTGAGTTTT[G/T]GCTCATCTGTTGATG | 79658 |
| rs185221500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147773312 | AAGTTCACCCAGTTC[A/G]TCACAAGTTAGAATT | 79658 |
| rs185229365 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147946263 | ACAACTGAAAGTGCC[A/G]CTTGCTATAAGCCAA | 79658 |
| rs185229829 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147829311 | CCTGCCTCGACCCCC[A/C]CATCGTGCTGGGATT | 79658 |
| rs185230993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147807527 | GTCGGTGTATTTTAA[A/G]TGTGTAAGTGACAGA | 79658 |
| rs185241644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147829618 | TCTACTCACTTCTGC[A/G]CGTGTTCTCAGAGGA | 79658 |
| rs185246684 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148003058 | TGGGCATTTAGTGCT[A/G]TAAATTTCCTTCTAC | 79658 |
| rs185247525 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147908757 | AGAATACAGCAGTTT[A/C]CTTATCACTCCATAG | 79658 |
| rs185249414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147812653 | ATTTTGATTATTCAC[A/G]TACATTTTACAAGGA | 79658 |
| rs185250908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147965203 | CTCTGGGATTTGTGA[C/T]GGGTGGAACTGGGGA | 79658 |
| rs185255759 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147759626 | GACATTAATTTTAAT[A/G]TTTTACTTAATCTGG | 79658 |
| rs185259029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147999321 | TGAGCCATCAATGGC[C/T]ACCCTCTTTGGGTAC | 79658 |
| rs185263024 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147865730 | ATAGAAACAAGAATA[A/G]CCAAGTAATGATTAA | 79658 |
| rs185263710 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147777148 | ATATGCATGATTTGC[A/G]TTTCAGCTATGTATC | 79658 |
| rs185263813 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147735580 | GGCCATAAAAACAAG[G/T]TTAGGAATGTGGACT | 79658 |
| rs185266076 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148016520 | GAAAGAAAAAAAAAA[A/T]TGAGGGAAAAAATGC | 79658 |
| rs185274654 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147866067 | TCAGAGCCCCAGATT[C/G]CTAACCACCCACGGT | 79658 |
| rs185277680 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147847909 | TGAAATTACCCCAGA[G/T]AAATAATTTCCACCG | 79658 |
| rs185283401 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147904562 | ACAAGGACATGAGCT[C/T]ATCATTTTTTATGGC | 79658 |
| rs185316432 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147750118 | CTTTGTATTTTTTGA[C/T]CTTAAAATTTTCATT | 79658 |
| rs185349416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147811877 | CAAATGTACCCCTTA[A/G]CTTTTGGAGCAGAAA | 79658 |
| rs185352997 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148059433 | TACTAATCAAAAATC[C/T]GTAGTTAAAGGGACA | 79658 |
| rs185362625 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148030233 | AAATTCTTTAAAGCT[A/T]CTCTCCCTGTGGAGT | 79658 |
| rs185363849 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911609 | CTTCGTGATCCGCCC[A/G]CCTTGGCCTCCCAAA | 79658 |
| rs185367449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147788092 | CAAACACACCCCTGC[C/T]GTTCCACATGGACAC | 79658 |
| rs185370212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147884487 | CCTTATTAAAGAGGC[A/G]TAGGGGCCTGGATTC | 79658 |
| rs185378415 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147847322 | AAGGAGATGCCGGAG[A/C]AAACCATCTGTTGTT | 79658 |
| rs185389610 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147738659 | AAGGTTAACAATTAT[G/T]ATGACATAACTAAAT | 79658 |
| rs185393313 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147826422 | TGTCTGTATAAGGCC[A/G]TGAACCTTAGGAGTG | 79658 |
| rs185395424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147755951 | GTAACAGAATAGCCA[A/G]TTATCAACTGGCTTT | 79658 |
| rs185399687 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147808776 | TGGGCCCCCTCTGGT[C/T]CTGCACTCTTCTAGG | 79658 |
| rs185402185 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148000960 | TAAATTTTGGCTTTT[A/G]TTGCCATTGCTTTTG | 79658 |
| rs185407445 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147774659 | TACAAAGCTTCTTGT[A/G]TGTTGTGGAAGATAG | 79658 |
| rs185407983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147908931 | TCTTTGCATCTGAGC[A/G]TATGATAGTGTGTTA | 79658 |
| rs185411810 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148031934 | TAATTTATGCCACCA[C/T]TTACCTAAATGAACA | 79658 |
| rs185415833 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148013557 | GCCGGGCATGGTGGC[C/G]GGCGCCTGTAGTCCC | 79658 |
| rs185418696 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147862231 | GCATGCATACCCGGC[A/T]GGGTGGCAACAGTAC | 79658 |
| rs185423532 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147979507 | CTTAGGATTGCCTTG[A/G]CTGTTGAGGCTTTTT | 79658 |
| rs185423821 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147944012 | TGGTAGAAAGCTGGA[A/T]ATAAAAGATTTCCTT | 79658 |
| rs185433533 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147844309 | AATAGGGTATCCATC[C/T]GTTCAAGCATTTATC | 79658 |
| rs185434730 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148070117 | TTATATGTGTTACAT[A/G]CTCTCATAGTCTGGA | 79658 |
| rs185452775 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148007363 | TGTCATCAGGGAAGG[A/G]AGGGAGCTCGGATTC | 79658 |
| rs185472122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148012791 | TGAGGTCCATATATA[A/G]TTGTATTAAATATAT | 79658 |
| rs185480376 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148034344 | ATTTTTTTGAGACCA[G/T]TTCGCTCTTGTTGCC | 79658 |
| rs185482500 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148050334 | TGAATGTCTCTTAGG[A/C]TACTACATTTGGTTT | 79658 |
| rs185521495 | snp | A/G/T | 0.00319074 | 0.0398324 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147926585 | AAGAAATAGAATGAA[A/G/T]GCAAGAGGAGAGATG | 79658 |
| rs185533226 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147866481 | GCAGAACATGCCATA[A/T]AAGCTGTCTAATGGC | 79658 |
| rs185547294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147848231 | TGGAATGAATTCTCA[C/T]TTAAGTGACTTGTGA | 79658 |
| rs185559751 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147906387 | GTTATTGTTCAACAG[A/G]TACAGAGTTTCAGTT | 79658 |
| rs185562165 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147961867 | ATGACATCGTACCTC[C/T]CTGGTCCTCCCACCT | 79658 |
| rs185568047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148010553 | AGTATAATTCTATTA[C/T]TGCTATTTTTGTTGA | 79658 |
| rs185568974 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147923134 | GGTTGGAATTGGTAC[G/T]TTCACATAACATGTA | 79658 |
| rs185569277 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147996627 | GGCAATGACCAGGCT[A/G]CATAGATGCCTGGCT | 79658 |
| rs185577018 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147957821 | ACAAATATAAATTTC[A/G]TTTCTATTTTGTCAC | 79658 |
| rs185595594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147977638 | TTGAAATCTCAGCTC[C/T]ACTCAATTGTGTGAC | 79658 |
| rs185595928 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148049444 | ACACTCTTCTAGGGT[C/T]GTGCGTTGCTGTCCT | 79658 |
| rs185597516 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147941431 | CAGTCCTTAACTTAC[A/G]AGGTGTTTTTAAATA | 79658 |
| rs185616739 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148055505 | AGCAGCCTGGCCAAC[A/G]TGGTGAAACCCTGTC | 79658 |
| rs185619530 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147767107 | CCACCCACTTTGGCC[A/G]CCCAAAGTGCTGGGA | 79658 |
| rs185631589 | snp | A/T | 0.0178098 | 0.0926698 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147783746 | TTATGTATTGTATAA[A/T]TTATAGAACACATTA | 79658 |
| rs185652659 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147733375 | GCAGCCTGACCATCC[C/G]TTGGATCCATAACCC | 79658 |
| rs185667035 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147751458 | AACCTCCGCCTCCTG[A/G]GTTCAAGCAATTCTC | 79658 |
| rs185702022 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147941271 | TTGTTCCTGTTCAAG[A/G]AAAGTTTGAACAAGG | 79658 |
| rs185706382 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147976703 | TTCTGTTTTTCTTTA[G/T]CTGTGGCATTGGAAG | 79658 |
| rs185710541 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147806094 | TAACTCACAAGAACT[A/G]CCATGCACACATACT | 79658 |
| rs185711551 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147918275 | TGAGTAGCTGGGACT[A/C]CAGGTGCCCGCCACG | 79658 |
| rs185717663 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147963963 | CCTACTTCAGTTATG[A/G]TCTCATCTAAACTGA | 79658 |
| rs185719418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147882143 | ATTTAGTTAGGAGTC[A/G]TTCTAACCAGGGTTG | 79658 |
| rs185722866 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148029663 | TTTCTCCATGCTTAC[C/T]AATTTTTTTTTGGCA | 79658 |
| rs185723745 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147903036 | ATCAAGTCACCTCCC[A/G]CCAGGCCCCTTCTCC | 79658 |
| rs185730919 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147771861 | CAGTGGTGCTATCTC[A/G]GCTCACTGCAACCTC | 79658 |
| rs185733384 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147980990 | GTTAATCCTATCAAT[C/T]TTGTTTATCCTTTCA | 79658 |
| rs185736021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148066922 | GTAGTGTGCCATAGA[C/T]GAGGCTACGCTTTGA | 79658 |
| rs185738819 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147746035 | CCTCGTGATCTTCCC[A/G]CCTCTGCCTCCCAAA | 79658 |
| rs185743701 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147938212 | ACTGAGGCCTATGGG[A/C]GGGTGGAGGGTGGGA | 79658 |
| rs185745364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148008254 | CTGAAAGCATCTTGG[A/G]TGCACTTCTTGCTCA | 79658 |
| rs185746879 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147842288 | CCTTTGGGGCTCAGA[C/G/T]GGATATTGCATTGAA | 79658 |
| rs185749741 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147997628 | TATAGAACCAGACAC[A/G]TAGAACAGAAATAAC | 79658 |
| rs185751137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147954449 | TCAATATGAAATGAC[C/T]TTCTTTATCTCTGGC | 79658 |
| rs185751287 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148025814 | TTTAATTTTTTTGTA[C/T]TTTTTTCTTATTTTA | 79658 |
| rs185765988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148044850 | AGCAGTGGTCTACCA[A/G]TGGGTTTTGGTCCAT | 79658 |
| rs185770320 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148064189 | TGGTTCAGTGACAGC[G/T]CCTCAGAGAGGCTCC | 79658 |
| rs185771451 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147763301 | GGTGGTGTTTGTAGT[A/C]GGAGTAGATAATAGT | 79658 |
| rs185775860 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147780850 | TCTGAGAGCAAGTCC[A/G]CCTAGGGTGGACTGG | 79658 |
| rs185777155 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148027755 | ATGATATAAATTAGC[C/T]GTCTTAGGTAGGTTG | 79658 |
| rs185786504 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147799732 | ATTTATAATTGATTA[C/T]TGAAGCACTTGTAAG | 79658 |
| rs185791049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148065656 | CTGAAGGGGAGGGTG[C/T]GATGGTAGTATTGAA | 79658 |
| rs185800526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147753780 | TTTCATGATGCTCAC[A/G]TATTCATGAATGTTG | 79658 |
| rs185806723 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147746830 | TTATGGCAGGACATC[A/G]AGGAAACTGTCAACT | 79658 |
| rs185840906 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147818295 | GTTAGGCTGGGCGCG[G/T]TGGCTCACGCTTGTA | 79658 |
| rs185863100 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147860546 | TGCTGCTATACCTCT[A/G]TGTTTATTGGGCATA | 79658 |
| rs185869858 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147786181 | GGTTATTAAGAGGAA[C/G]TAACCTTATTAGCTG | 79658 |
| rs185874568 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147784743 | TAAAATATATATTAT[A/G]AATATATATTATAAA | 79658 |
| rs185886115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147825073 | CAGCTGGCTTCGTAG[A/G]TGTCACTCTAATTTC | 79658 |
| rs185889466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148009006 | ATGGTTTAGTATTAA[A/G]TAATACATATATTTA | 79658 |
| rs185905391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148046597 | TTTATACCTGGACTC[C/T]GTATAGTGAGGAAGT | 79658 |
| rs185906470 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148022164 | TTTGTTTTTAAATTA[G/T]ACATGTGCAGAACGT | 79658 |
| rs185912105 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147884925 | TCAAAGCTCATTCTG[G/T]CAGAGTAAGAAAGAT | 79658 |
| rs185914335 | snp | C/T | 0.0018771 | 0.0305782 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147822893 | ACTCCTTTCTTCTTA[C/T]AGATGCTTCCTTACG | 79658 |
| rs185915387 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148040168 | GTTCTTGTCCTTGGG[A/T]TAGGCCAAATCATCC | 79658 |
| rs185919959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148061781 | ATGGCTCCATGTCCC[C/T]GCCAATCTGCCTGGC | 79658 |
| rs185923599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147777898 | CTTTCCTATAGATGG[A/G]GAGATAAAACTTGAG | 79658 |
| rs185929788 | snp | G/T | 0.0554779 | 0.157039 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147793158 | AAAGAAAATGTGTGT[G/T]TATGTATGTGTGTGT | 79658 |
| rs185946901 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147840456 | AGCATTCTGGTTACA[C/T]TCCTGCTTTACCCCA | 79658 |
| rs185953999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147858789 | TCTCACCTCCATTTT[C/T]AGGTATCCAAAAAAA | 79658 |
| rs185956381 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147822122 | TAATCTCCAATTAAG[A/T]TGAGGACCTCTGTAG | 79658 |
| rs185962794 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147803906 | TAAACATGAGGTGTG[C/G]AGGTTTCCCTTTGAT | 79658 |
| rs185974678 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147762687 | GGTGCCTGCCACCAC[A/G]CCCGGCTAATTTTTT | 79658 |
| rs185979488 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147876127 | TAGAAGTTAATGTTC[C/T]ATGCAGGCAGCAGGA | 79658 |
| rs185983952 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147857872 | TATGGATTCATAGTA[C/G]TAAAATTTTTGTTTC | 79658 |
| rs185999440 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147768495 | CATCACAGTGGTCTC[A/C]CTAATTAAAAAAAAA | 79658 |
| rs186005758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147913850 | CATTGTTGTGTGGGT[C/T]CCTGTTTAAAAAAAT | 79658 |
| rs186009935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147933445 | TTGAGGGATTAGCTG[C/T]TTATTTTCATCTACC | 79658 |
| rs186012287 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147740995 | TTGCATGTGTTTAAA[A/C]TTTATATAATGGTTT | 79658 |
| rs186035326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147841336 | TGATTATGTAATCTG[C/T]ATGTGTGGTTATAAA | 79658 |
| rs186041558 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147799052 | TTTTTTTTTTCTCTT[A/C]GAGATGGAGTCTCAC | 79658 |
| rs186050327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147834155 | AGTCACCAGTCTACT[C/T]CTGTGATAACCCATT | 79658 |
| rs186053930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147804161 | CCTCCTCCTACCCTC[C/T]ACCCTCAAGTAGCCC | 79658 |
| rs186068508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147876950 | CTAAATGCTGGAGTT[A/G]TCATTCTGAACCTGG | 79658 |
| rs186082080 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147863153 | AGTGGTATTAAGTAC[A/C]TTCACATTGTTTTGC | 79658 |
| rs186088394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147844805 | TCGTGTACCACTCTA[A/G]AAGCCTCCTAACGAG | 79658 |
| rs186088882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147853707 | GTTGTAATCCTCCCC[C/T]CTTTGCTGTGTGCCC | 79658 |
| rs186089998 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147937950 | CTCCATTGTACTCCA[G/T]CCTGGGCAACAAGAG | 79658 |
| rs186091474 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147902409 | CTGCTGCAAAGAACT[G/T]CCTGAGATTGGATAA | 79658 |
| rs186094419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147746462 | CTGGAATGCAGCGGC[A/G]CGATCTTGGCTCACT | 79658 |
| rs186097154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147835675 | CACTGCGCCTGGCCT[A/G]TTTTATTTTCTTGAT | 79658 |
| rs186103031 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147818509 | AGGCGGAGTTTGCGG[C/T]GAGCTGAGATCTTGC | 79658 |
| rs186107434 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147800715 | GAGTTCTCCTTTGGT[A/T]ATCTCCTCTGCTATT | 79658 |
| rs186111601 | snp | C/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147890653 | CCAACCTGGTGAAAC[C/T]CCATCTCTACTAAAA | 79658 |
| rs186113732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147937105 | AAAATTGTCTTCCAT[A/G]AAACCAGCCCCTGGT | 79658 |
| rs186123374 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147972580 | AGATTTTCCTGTTAG[G/T]GGTAATAGAGGAGCC | 79658 |
| rs186123721 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147871455 | AAAAGTTTTTTAAAG[A/C]TGTTTTCTCTTTCAA | 79658 |
| rs186129855 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147917170 | GGCTCTACTTCCTTT[A/G]TTTGGAAACTGTCTT | 79658 |
| rs186139555 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147817217 | CCCATTAGTGCTTTC[A/G]TTGCTGGGGTGGGAA | 79658 |
| rs186146910 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147953965 | TTGTGTTTTTATTTC[A/G]TTCTTTTCAGAATAC | 79658 |
| rs186149006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147910534 | TTGTAGTGTTTGACT[A/G]CAGGCTATACAGATA | 79658 |
| rs186158288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147812920 | AGTACTCACTTGGAG[C/T]AGCGACTGGCACAAA | 79658 |
| rs186166057 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147780324 | ATTCTGCCCTACCTC[C/T]CCTCTCCTACCCAGT | 79658 |
| rs186179284 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147777351 | GCAAGCTCCACCTCC[C/T]GGGTTCACGCCATTC | 79658 |
| rs186187850 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147881738 | AAAGAGAAGGACTTA[A/T]GATCTTGAACCTTGC | 79658 |
| rs186215460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147917695 | ATTTTATAGATGTTG[A/G]TAGAAGAATAGGATT | 79658 |
| rs186247787 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147959247 | TATTTTTTTTTTTGT[C/T]TTTGAAGAAGAGGGA | 79658 |
| rs186248443 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147990187 | TCATTTGAATTCTTA[A/C]GAATGTCTCCCAAAT | 79658 |
| rs186249333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147915166 | CGGCGGAGTAGGAGC[C/T]GTTGTATGATTTGGG | 79658 |
| rs186254987 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147954167 | CTGGGAATGTGTGTT[C/T]TGCTTTTGAGTGGAG | 79658 |
| rs186262610 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147933757 | GCAGGTCTCTGCATG[A/G]GTGGGATGAATTTCT | 79658 |
| rs186263992 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147994445 | TACCAGAAGTGCACA[C/T]GGGCTACAGATTTTA | 79658 |
| rs186266532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147985777 | GTGTGTCCGTCTCAG[C/T]GTCTGTAAGCTTTTC | 79658 |
| rs186267029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147949059 | AGGTAGCCTGGGTTG[C/T]CTGGTTGTCCCACTT | 79658 |
| rs186271120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147949884 | TTTCTTTTGCTGTGT[A/G]GGAGGAATTTGTTTA | 79658 |
| rs186272488 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148005905 | CATGCAAATTACCGT[C/G]TCATTACACAATATT | 79658 |
| rs186274874 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147978068 | TCCACTCCACTATTG[A/G]TGGGCACTCTATTGA | 79658 |
| rs186276972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147914414 | CCAGGCTGGAGTGTG[A/G]TGGTGGAGCCATAGC | 79658 |
| rs186278063 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148006275 | AGCTGTTCCAGCTTT[C/G]CTGTCCAGGCACTGG | 79658 |
| rs186282388 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147967514 | ACCCAGGTGATCCAT[A/G]TTGGGGTGAGCAGAA | 79658 |
| rs186289079 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148039909 | GGCAATTTCACTTCT[A/G]TTCTCTATATTACAA | 79658 |
| rs186306780 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147985022 | GTGCCTAGGTGTGGA[A/G]CTGGGAACCTCACCT | 79658 |
| rs186316395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148013272 | TATGTAAGTCATTCC[C/T]GTAAACGTGTACTTG | 79658 |
| rs186323050 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148000823 | TTGTGATTCTGGATA[C/T]TAGCCCTTTGTCAGA | 79658 |
| rs186337918 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147792973 | GTGAAACCCGTCTCC[A/G]CTAAAAATACAAAAA | 79658 |
| rs186348401 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147830453 | CCAAACTATTAGGTT[G/T]GTACAAAAGTAATTG | 79658 |
| rs186365109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147927759 | GGGAGCTTGATCCTA[A/G]GGGAAGGCGCAGAGG | 79658 |
| rs186392162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147934810 | CTGCATTCCACCTGG[A/G]TGACAGAATGAGACC | 79658 |
| rs186398966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148046035 | AGTTAAAATTTAATG[A/G]GGACTGAGGATTAGG | 79658 |
| rs186399163 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148064612 | TGTCGGGAGGGCGAG[G/T]CTCCCCCTTGATGCT | 79658 |
| rs186399755 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147990551 | CAATCCAAATGCCCA[C/T]GAGTGGTAGACCAGA | 79658 |
| rs186405880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147896987 | TATGTATTGAATATC[A/G]AAAGGATTTTTTTGC | 79658 |
| rs186408323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148016967 | CCTGGGCAACATGGT[A/G]AAACCTCATCTCTAT | 79658 |
| rs186418109 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147994320 | AGTCATGAGCTTTAT[A/G]TAGTTGCTTGAGCCA | 79658 |
| rs186428733 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148021510 | GCATCTGCCATATTT[C/G]TAAACATCAAACATA | 79658 |
| rs186433288 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147968684 | AGATTTTTTTTTCTT[C/T]AGTCACCTGTAGATG | 79658 |
| rs186448616 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148061368 | CTTGGCAATTGTTTG[G/T]CTAACTGTGGCCTTA | 79658 |
| rs186465018 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148057099 | CCTCTGGGGGGCACT[C/T]GTAAGTCATTCGCTT | 79658 |
| rs186507453 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148040813 | TTTATTAAAAAAGAT[C/T]TGGGGGGGGTTATTT | 79658 |
| rs186509013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147742181 | AATGAGTGCTTTCTT[C/T]TCTGACTGTAAAGTT | 79658 |
| rs186519331 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148062504 | TAATTCAGATTAACA[C/T]GCATCAATTATTTGA | 79658 |
| rs186554130 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147945399 | ACTGACTTACCATTT[A/G]AAAGGATGTTTGTAA | 79658 |
| rs186556448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147755822 | GTGTGTGTGTAGTGC[A/G]TTATGAGTCAGCCTC | 79658 |
| rs186595192 | snp | G/T | 0.0517044 | 0.152246 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147738022 | TGTGTTGTTGTTGTT[G/T]TTTTTTTTTTTGAGG | 79658 |
| rs186599624 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147973045 | CAGGCATGAGCCACC[A/G]TGACTGGCCTAATGG | 79658 |
| rs186615087 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147772069 | TGCTGGGATTACAGG[C/T]GTGAGCAACCGCGCC | 79658 |
| rs186625751 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148018320 | TGGGCACTAAGAGGA[A/G]TTTGCATCCAGGCAG | 79658 |
| rs186626622 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148003393 | GAATTTATATTCTGT[C/T]GATTTGGGTTGGAGA | 79658 |
| rs186635955 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148037039 | TGGTTTTTCTGTGTT[C/G]TTTGGTCATGATCTT | 79658 |
| rs186639643 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147831697 | AATTCTCTTTTTCCC[A/G]TAAGCCTGTTATTCA | 79658 |
| rs186639673 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147778132 | GAAGTGTCGGTTTAG[C/T]GCTGAGAGGAGCAAA | 79658 |
| rs186640436 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148058848 | CCCCGAAATTCAGGC[C/G]CATGTTTCCAAGCAA | 79658 |
| rs186642546 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147753902 | TTTGTGGTTAGAGAG[A/G]TTAACAAATTGAGCA | 79658 |
| rs186643975 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148035059 | GACCTTTGCAAGAGG[A/T]AGAGGTGGTTCCTGG | 79658 |
| rs186647999 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147793789 | TACGTGCCTTCCCCC[C/T]TAACAGTAAGCTTCT | 79658 |
| rs186648243 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147814891 | CAGGTTCTGGGGGTT[G/T]GGATTTCAGTATATA | 79658 |
| rs186699970 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147853292 | CAGTGGCCCTGGCCA[C/T]GAATCGGTTTTTATT | 79658 |
| rs186728873 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147759987 | ACTCCTGACCTCAGG[C/T]GATCCACCCGCCTCA | 79658 |
| rs186752530 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147890317 | CAATGGTTAGATGGA[A/T]GTGTGCTTCATTTTT | 79658 |
| rs186767364 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147846551 | GAAAATGTGGTTGTG[G/T]CTGGAGTTTGTGTGT | 79658 |
| rs186770935 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147776063 | ATTTTTTGAGATTTC[G/T]AAGACTTTTGATAAT | 79658 |
| rs186772005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147734464 | AGTGTCTTTTTTTCT[C/T]GTTATGTTCATTAAG | 79658 |
| rs186772505 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147890758 | CTTGAACCCGGGAGA[C/T]GGAGGTTGCAGTGAG | 79658 |
| rs186773757 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147828049 | ACCTTGTGATCTGCC[C/T]GCCTCATTCACCCAA | 79658 |
| rs186779345 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147790385 | GCAAACATTCAGTTC[A/G]TAACACCTAGTAATA | 79658 |
| rs186783413 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147810104 | TTCACCCTTTTTGAG[C/T]GGGAAGAAGAAAGGA | 79658 |
| rs186796354 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | ARHGAP10 | GRCh38.p7 | 4:148072928 | GAGCCTGGAGTATTC[A/G]GGGTGGGGCGTGTTC | 79658 |
| rs186800432 | snp | A/C/G | 0.0926964 | 0.194308 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911569 | GGGTTTCACCGTGTT[A/C/G]GCCAGGATGGTCTTG | 79658 |
| rs186804651 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147884005 | TAGCTTGAGCCCTAC[A/C]TCTTAACCACTGTGC | 79658 |
| rs186804897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147864381 | CCATCACTCCCTGAG[C/T]GCTGAGGTGCTGGGC | 79658 |
| rs186836290 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147737588 | AGGGTAATTTTTTCC[C/T]GAATGGAAAGGAATA | 79658 |
| rs186852014 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147767587 | ATCTAGGCATAAGTG[C/T]GCACCTGTAGTCCCA | 79658 |
| rs186878071 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARHGAP10 | GRCh38.p7 | 4:147731482 | AGAAGTGTAATAGGA[A/G]CTGCTGGGCCACCAA | 79658 |
| rs186894763 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147831274 | GATGGAAAGCCTAAG[A/C]TTTGACTTCTCATTT | 79658 |
| rs186901928 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147887016 | CCTGCCTCGGCCTCC[C/T]AAAGTGCTGGGATTA | 79658 |
| rs186904713 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147907162 | TTTCATCTAGTAGTT[C/T]ACAGTATGCAGTATT | 79658 |
| rs186905421 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147868637 | CAACCTTTTTGGCAC[C/T]GGGGACTGGTTTTAA | 79658 |
| rs186919475 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147942826 | CCTAAGGCAGCTATC[C/T]GCTGGATTTCCAGCA | 79658 |
| rs186923483 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147867142 | TTGAATTTATAATGC[A/C]CTACTTAACTGGGCA | 79658 |
| rs186930795 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147834834 | GACCTGCATCACTGT[C/T]TGATGGCCCCTCCAG | 79658 |
| rs186931026 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147908373 | AGTCAGTTTGCGTAG[C/G]GAAAAGACTAAGTCA | 79658 |
| rs186937635 | snp | A/G | 1.68281e-05 | 0.00290065 | synonymous-codon, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147966836 | AATTGAAAACCATGA[A/G]AAGGTAAAATTTTTT | 79658 |
| rs186941678 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148000754 | CTGTTCGTATCCTTC[A/G]CCCGCTTTGTGATGG | 79658 |
| rs186953205 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147942219 | AAGGAACATTTTGTT[A/T]GTAATGCATTGTCTT | 79658 |
| rs186954074 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147961155 | CAGAGTGGTTGAACC[C/G]TTTAATGATTACCAT | 79658 |
| rs186954839 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147910202 | TTAATTTTTTTGTTG[G/T]TGTTGAGATGGGATC | 79658 |
| rs186956184 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147995718 | TTGCATGGTCCATCT[C/G]TCTCTCTTTTTTTTT | 79658 |
| rs186961575 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147978970 | TTAGTTCTTTGTCAG[A/T]TGCATAGTTTGCAGA | 79658 |
| rs186964841 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147871254 | TGAGCCACCACGTCC[A/G]GCCGTGTGTGTGTTT | 79658 |
| rs186981683 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147784815 | AAATATAATATATTA[C/T]AAAATATATATTATA | 79658 |
| rs186984827 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147843451 | TTCTGCCACCTTGCC[A/G]TGGATATTGCTGAGC | 79658 |
| rs186989519 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147751676 | CTGGCCTTTTTTTGC[C/T]TTTTTTGGAGCACTT | 79658 |
| rs186996869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147808509 | TTAAGCAGGGGAGTA[A/G]GGAGATCCAATTCAT | 79658 |
| rs187008666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147823924 | TAAAAGCTTACATTA[C/T]CTTCCTAATGATATT | 79658 |
| rs187011303 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147881093 | GGCCTGGCCAACATG[A/G]TGAAATCCTGTCTCT | 79658 |
| rs187012694 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147781186 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAAAT | 79658 |
| rs187014572 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147752951 | AGAAGTATTTTTATT[C/T]TCTTTGGTGATGGTA | 79658 |
| rs187020169 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147805122 | GTTTTACATTGAAGT[C/T]TTTAATTCATCTTGA | 79658 |
| rs187021110 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147768972 | TGAACTCCTGACTTC[A/T]AGTGATCTGCCTGCC | 79658 |
| rs187042850 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147813438 | CCGTGGGAAAAACAT[A/G]AGCCAAGCCAATTTG | 79658 |
| rs187053680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147841857 | ATATAGTGTTATTTG[C/T]CACAACTACTACTAT | 79658 |
| rs187056193 | snp | A/T | 0.194902 | 0.243853 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147784176 | ATTGTGTATTATATA[A/T]TTTACATAACATTAA | 79658 |
| rs187065196 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147945617 | ATGTTAATTTCAGAA[A/C]GATAGTCTAATGAAC | 79658 |
| rs187065725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147940325 | TCTCAGGGATTCATT[A/G]GTATTCACAGTGGCT | 79658 |
| rs187074366 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147982489 | ACAACCCTCCCATGT[C/G]AGCTTCCTAAGACTG | 79658 |
| rs187080060 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147848673 | GAATTGGATGGTGCT[A/T]TATGTGTGACGGTTA | 79658 |
| rs187081615 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147921536 | TCTGGGTCATGGTGC[C/T]ATATAGCATTTGGGA | 79658 |
| rs187082902 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147975490 | ATTTCATTTCTTACA[A/G]TTGCATAAGCTGGAA | 79658 |
| rs187084275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148009418 | ATTATAGCCATGAGG[C/T]GCCATGCCTGGCCGA | 79658 |
| rs187085877 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147999452 | CCACCACTGCTGTTC[A/G]CTGCCATTGCAGCCC | 79658 |
| rs187091654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147957120 | TGTGATAGTCTTCAC[A/G]GTGATTTGGATGACA | 79658 |
| rs187092902 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148028703 | TGACTTAATCTGCCA[C/G]TAGAAATCTGAAAGG | 79658 |
| rs187098156 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147981139 | GTTTTTCTGGTTTCT[G/T]TAGGTACAAGGTTAG | 79658 |
| rs187101239 | snp | A/C | 0.000170227 | 0.00922413 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148046853 | AGTTTTTTCTTCTCC[A/C]GGTATTTGTTTGATA | 79658 |
| rs187107201 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147948140 | GTAGAGACAGGGTTT[C/T]GCTGTGTTGGCCAGG | 79658 |
| rs187116037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148066624 | AATACCAGTGTCTCC[A/G]TGTGTTTTGGAGGAG | 79658 |
| rs187122210 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147886502 | GTTAAGCCCTACAGT[C/T]TGTTGTTCGTCGTGC | 79658 |
| rs187126970 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148008466 | ACAGTTTTGGTGATC[C/T]CCACTGGGGGTGGTG | 79658 |
| rs187134518 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147923737 | TTGGAAAACCTTACC[G/T]CTTGAAGATTGCTTT | 79658 |
| rs187140861 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148014868 | AATAAAACATAAACA[A/G]AATTAGAAAAACAGA | 79658 |
| rs187149059 | snp | C/G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147984296 | CCACTGGAGAAGCCC[C/G/T]AGGAAGCAGTTTCTT | 79658 |
| rs187170997 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148033689 | CTGTGTTTCATACTA[A/G]TGTGTTGGGTATATG | 79658 |
| rs187175308 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148053445 | TGAATCTGGTTGCTG[C/T]GCATTTATCATCTAA | 79658 |
| rs187196820 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147825883 | TGTTGAGAATCTCAG[C/G]ACAAAGGTAAAGGCA | 79658 |
| rs187213914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147764442 | GACTTTGAAGTGTGG[C/T]TGATCTCCCATCGGC | 79658 |
| rs187218892 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147979291 | GCCAGTTTTCTCAGC[A/T]CCATTTATTGAATAG | 79658 |
| rs187222221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147861501 | GTTACAGCTCTTTCA[A/G]TCTGGCCATTCCTTG | 79658 |
| rs187226181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148007105 | CTTGGACAAAAATCT[A/G]TATAGAAGAAGAAAA | 79658 |
| rs187230215 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147996196 | TCTTTTCAGAGAAAG[G/T]AGAGAATAGCTAGGA | 79658 |
| rs187246313 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148024086 | TTTTCAACACTGATC[A/C]ATACAAAACAAGACT | 79658 |
| rs187247568 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147901909 | ATCAGTGGAAAACTT[G/T]AGGGGAAAACAAAAA | 79658 |
| rs187249295 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148042558 | GCAATAATTTCTTCC[C/T]TTTCCTGTTGCTGCA | 79658 |
| rs187255355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148063433 | CCTGGACTTCATGGA[C/T]AGCACTTACCACCTT | 79658 |
| rs187266717 | snp | A/G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147928834 | TATACTACAATTAAA[A/G/T]CTTGTAATGATTGCT | 79658 |
| rs187279685 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147964217 | CAGGCTGTACTCTCC[G/T]GCCCTTGTCACTTCA | 79658 |
| rs187282886 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147998700 | ATACATTAGTATATC[C/T]TACTATTAAGTGAAA | 79658 |
| rs187293546 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148026437 | CCAATTGAGAGATGA[A/C]CAGTTTAACTAAATA | 79658 |
| rs187296312 | snp | C/T | 1.64779e-05 | 0.00287031 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148023300 | CTACATTCCCTGAGC[C/T]CACCTGCCTGTCAGC | 79658 |
| rs187296681 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148050460 | CTCACTGCAAGCTCC[A/G]CCTCCTGGGTTCACG | 79658 |
| rs187325965 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147736150 | TGTGTGTGTGTGTGT[C/G]TGTGAAGCTAAAGGG | 79658 |
| rs187384559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147773687 | TGTTAAAAAGCATGC[A/G]CTCTGTGTACCAAAA | 79658 |
| rs187393552 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147747433 | GAAGAAACAATGCCT[A/G]GAAGAAATAAATGCT | 79658 |
| rs187437398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147975341 | TCAAAGTCCCCGAGT[A/G]GTGTGTGTCCTCCAG | 79658 |
| rs187445284 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148003927 | GTGAAGAACACCTAT[A/G]TGAAGAAAGCTGCAA | 79658 |
| rs187453053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147743074 | AGTCTCACTCTGTCA[C/T]CCAGGCTGCAGTGCT | 79658 |
| rs187453240 | snp | A/G | 0.0154538 | 0.0865337 | upstream-variant-2KB | ARHGAP10 | GRCh38.p7 | 4:147731972 | GCGGAGGAAAGAGAA[A/G]GGGACGAGCGGGAGC | 79658 |
| rs187459744 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147760609 | TGATGGACTTACTCT[C/G]TTGGACATACACAGA | 79658 |
| rs187484121 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147801569 | GTAAAATAACATACC[A/G]TCTGTTTTTTACTAT | 79658 |
| rs187485322 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148029785 | GGAATTACTGTGTTG[C/T]GAAGTTTAATCTAAG | 79658 |
| rs187490798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148066972 | GGTTCTGTGCTCTGC[A/G]GTGCTGGTATCCAGC | 79658 |
| rs187500218 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147749119 | TTCTATTTTTTTCCC[C/T]GTTGCTTGGTTGATT | 79658 |
| rs187500411 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147836842 | TGATGTGCCTTTTTT[G/T]TTTTAAATTGTTTTA | 79658 |
| rs187501137 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148030961 | CATGTTGGGTGGCCG[A/C]GGTGGGAGGATCAGC | 79658 |
| rs187504288 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147819499 | CATGAAATAAAATCA[G/T]CCTATTATATCTTTT | 79658 |
| rs187506743 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148006869 | GCTAAGATTTCCATG[C/T]ACCCTTTCCTTCCTC | 79658 |
| rs187507517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147766087 | GGAGTTTGAGACCAG[C/T]CTGGCCAACATGGTG | 79658 |
| rs187516025 | snp | A/G | 0.0498117 | 0.149749 | intron-variant, downstream-variant-500B | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147782926 | ATATATAAATTATAT[A/G]ATATATAAAATTATA | 79658 |
| rs187542983 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147775753 | TGGGGGCTCTAAATC[C/T]TTTTGCACAGAATTA | 79658 |
| rs187548704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147789168 | TGCTTTCCATTCAGT[C/T]GTGGAGAAGTCAATT | 79658 |
| rs187561955 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148068748 | GTCCTGTGGCAGTTC[G/T]GAAGTTGAGTGTGGG | 79658 |
| rs187562763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147739354 | TCTATAGTCGAGGTT[C/T]AGGCAGTCAGCAGCA | 79658 |
| rs187580139 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147760972 | AACTGTAAAAGAGCT[A/G]GTTGTAGGTAAAAAG | 79658 |
| rs187583829 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147756750 | TTGGAATATATCCTC[A/C]CTGGATAAGGGGGGA | 79658 |
| rs187601540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147824565 | GACTCACAGTTCCGC[A/G]TTGCTGGGGAGGCCT | 79658 |
| rs187624969 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147878252 | AGGCGCGTGCCACCA[A/C]GCCTGGCTAAATTTT | 79658 |
| rs187627776 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147860175 | AGGCCGGGCGTGGTG[G/T]CTCACGCCTGTAATC | 79658 |
| rs187630666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147842183 | CAAGTGATCCACCCG[C/T]CTCGGCCTCCAAAAG | 79658 |
| rs187642121 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147915672 | TTTTCTCATTTAAAA[A/G]TAAGAGACAAAAAGC | 79658 |
| rs187649768 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | ARHGAP10 | GRCh38.p7 | 4:147730769 | TGTAAGTCTATATCG[C/T]GAGTTTGTAGATGTA | 79658 |
| rs187651924 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147739862 | CGCCTCAGCCTCCCA[A/G]GTAGCTGGGATTACA | 79658 |
| rs187655491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147787409 | GATGAAGCTCATGAA[A/G]GTGAAAATGAATCAC | 79658 |
| rs187663149 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147898122 | ATGGTTTTCTTTATT[A/C]TTTTCTGCAAAACTG | 79658 |
| rs187674855 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147935458 | GGCAGACATTAGTCT[A/G]AAGTTTGAAGAAAGA | 79658 |
| rs187681260 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147950696 | TTTTTCTTCTACTGA[C/T]GAGGCAATTTTTTTT | 79658 |
| rs187683181 | snp | C/G | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147836560 | ATTTCCTATTAATCG[C/G]CTCCTGATTTTCAAG | 79658 |
| rs187697820 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147992039 | GAATGTGGCCATTAC[G/T]GGTTAAGGAAATTAC | 79658 |
| rs187704717 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147800876 | GAGTGCAGTGGCACA[A/G]TCTTGTCTCACTGCA | 79658 |
| rs187708830 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147872335 | AGGCTTCTTACTGTC[G/T]GGGAAAAAATTCACA | 79658 |
| rs187735657 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147904085 | ACCAGCAATGAATAA[C/G]AGTTCCTGTTGCTCC | 79658 |
| rs187741985 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147820259 | TTGCATGTTTGCCTG[G/T]TTTACATTAGGAACT | 79658 |
| rs187742381 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148049800 | TCATAAAATTGTTTT[C/G/T]TTTGTTTGTTTGTTT | 79658 |
| rs187760174 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147886827 | CCAGGCTGGAGGGCA[G/T]TGGCACCATCTCTGC | 79658 |
| rs187760975 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147940001 | AATACTTGTCATTCC[A/T]TTCCTCTACTTTCTA | 79658 |
| rs187779555 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147867425 | TCACTGACAAGCTGG[C/T]CAGGGTATGTTGAGT | 79658 |
| rs187790272 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147743434 | TTACTGTGTGACCTT[A/G]GGCAAGTTGTTTAAC | 79658 |
| rs187791192 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147837889 | TGCCTGATTGTAAGA[A/C/T]AACATTATTTTCCCA | 79658 |
| rs187799403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147955808 | TCACATAGACAGATA[C/T]TCGGATCTAAATTAC | 79658 |
| rs187801249 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147778623 | CCCCAAGAAGCTGCT[C/T]ATAGGGGTGTTGCTA | 79658 |
| rs187806077 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147931070 | GAGATGATGATGAAA[C/T]TTGACTGCTTCCCAC | 79658 |
| rs187809447 | snp | A/G/T | 0.0119091 | 0.0762411 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147893248 | ATTTTTAGTAGAGAC[A/G/T]GGTTTCACCTTGTTG | 79658 |
| rs187813855 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147938851 | GCAACTCATTTGAGA[A/C]GTAAATATAAGTCAC | 79658 |
| rs187825902 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147991192 | AATAGAAGTCTTTCC[A/C]TTAGGTCTAGGGCCC | 79658 |
| rs187829094 | snp | A/C/G | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147744931 | CTGCCGAGAGAGAAT[A/C/G]TAGAGGGAGAAGGCA | 79658 |
| rs187831950 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147973708 | CCTCCCCAGCCTCTG[A/G]TAACCATCATTCTGT | 79658 |
| rs187834825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147877714 | CCTGTGAGCCCTGAT[A/G]GTGGTACTGCTGACT | 79658 |
| rs187842275 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148003733 | GACTAGGATTGTAAC[C/T]CTTGCCTTTTTTTGT | 79658 |
| rs187847471 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147806112 | ATGCACACATACTGA[C/T]GGAGCTGAGTGACTG | 79658 |
| rs187850058 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147815566 | ATGTGATGACAGAAA[C/T]AAAGGTCAGGCTGGG | 79658 |
| rs187854286 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148035964 | TTTTTTAAAAAAGAT[A/T]TCTCTAGGTTCACAG | 79658 |
| rs187854349 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148017826 | AAATTTGCAGAGACC[A/G]TCTTATATCCTGTTA | 79658 |
| rs187878604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147850549 | AGTCACTGCAAAGGT[C/T]TGCGGCTTCACTCCT | 79658 |
| rs187918892 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147748031 | CAGGACAGCTCCCCT[A/G]CAATGAAGAATGATC | 79658 |
| rs187935861 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147781871 | AGTTAAATTCTTAGT[A/C]AGATTTGTATAATTC | 79658 |
| rs187940307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148006996 | CTTTTCTTGATTTAC[A/G]TATTTTTGCATAATA | 79658 |
| rs187945419 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147951737 | GGGTTACAGGTGTGA[A/G]CTACCATGCTTGACC | 79658 |
| rs187952539 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148041776 | GACCAATTGTGGTCA[A/G]TTTTTATGAGAATTG | 79658 |
| rs187958043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147970722 | ATTTTTCCTAGCCTC[C/T]TTGCTGTTTTTATAA | 79658 |
| rs187960158 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147936265 | TGTTTCTTAGCAACT[C/T]TCTTTTCTTTTTTCC | 79658 |
| rs187973014 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147986252 | TGAGCTACTCCATGC[C/T]TCTCACTGCCATTTC | 79658 |
| rs187980224 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147819169 | GTTTTAACTTTCCAG[A/G]GAACCTACTATTCTG | 79658 |
| rs187985014 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148014359 | TTCCAAATGTTTGCA[C/G]GTGCAAATTGATAAA | 79658 |
| rs187992825 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148001522 | TATGGCCATTTTCAC[A/G]ATATTGATTCTTCCT | 79658 |
| rs187993697 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147757610 | CTGCTGTAGCATTGA[C/T]AACTTCCATCCGTTC | 79658 |
| rs187994052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147854999 | ACCGCTGATTAAAGC[A/G]TCACCCCTTCCTCGG | 79658 |
| rs188002702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148033330 | ACATAGGCTTCCAGC[C/T]ATCCTGGGATGATAA | 79658 |
| rs188008469 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147930360 | ATCATCAATATATTA[A/G]TTGTTCATTTATTTT | 79658 |
| rs188014118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147854563 | GAACTTTTTGGATTA[C/T]GCTGTTACATTTATA | 79658 |
| rs188023855 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147891891 | TTCCCCCGCCCCAAC[A/G]ATTGTGTTATATAAC | 79658 |
| rs188030878 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147965300 | ATGCTTTCATGAAGC[G/T]GTATAATTATTTGCT | 79658 |
| rs188044703 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148060509 | TGATCCTTCCCAGCC[A/G]ACAAGCCTCTGAAAA | 79658 |
| rs188048306 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147956857 | CATTAGTATTATTAC[A/G]CCCCATAACTGATGG | 79658 |
| rs188054144 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147921157 | AGTGCAGATACAGCC[A/G]AATGATTTTGCTGAA | 79658 |
| rs188071417 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147992453 | CGCTCTGTTGCCCAG[C/T]GTGGAGTGCAATGGC | 79658 |
| rs188074422 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147761383 | GTTTTTCTCCTTTTA[C/G]TAGTAATCGCTGTAC | 79658 |
| rs188085839 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148018733 | ACAGTACTAGCTGGT[A/T]GTATTTTTCCCTAAG | 79658 |
| rs188104901 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148059084 | TGCTTTTAGTGAAAC[A/G]CTCTTGTTTCTATTT | 79658 |
| rs188105502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147966277 | ATGGGCAGATTCAAC[C/T]AGCTACTGATCAAAA | 79658 |
| rs188107274 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147885517 | GAGCTACAATTCAAG[C/T]TGAGACTTGGGTGGG | 79658 |
| rs188107427 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147932413 | CCCAAATGCCCATCA[A/G]TGATAGACTGGATAA | 79658 |
| rs188109478 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147906197 | GATATATACCTGAAA[G/T]AATTGAAAGCAGGGG | 79658 |
| rs188113005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147947778 | TCCAGTGGATACATT[C/T]GAATCAACTTATATG | 79658 |
| rs188121069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147983431 | AGCTCGTGATCCGCC[C/T]GCCTCCTCCTCCCAA | 79658 |
| rs188121869 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147832381 | AGTCCAGGCACGGTA[G/T]CTCACGCCTGTAATC | 79658 |
| rs188129870 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147859473 | GAGACAAGGTTTCAT[G/T]ATGTTGGCCAGGCTG | 79658 |
| rs188131482 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148011248 | TAGTGTTTTGAAACA[A/G]TCTTGTTATTTTCAT | 79658 |
| rs188135514 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148000316 | CACATTTTCTTAATC[C/T]AGTCTATCATTGATG | 79658 |
| rs188138318 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147795068 | AAGGTAGCAGCTGCC[A/G]GTCAAGGGTGGCCTT | 79658 |
| rs188139447 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147736716 | CAGTGGTTCTCAATC[A/G]TAGCTGCTCAATAAA | 79658 |
| rs188211018 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148032554 | TTTCCTGTCCTTCTA[G/T]AATTCTTTATTTTTA | 79658 |
| rs188225390 | snp | C/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148070965 | AGGCTGCAATTTTCT[C/T]GTTGAGTATCACGTG | 79658 |
| rs188227135 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148002396 | TGTTGTCTCTCTGCC[A/T]GGCTTTGGTATCAAG | 79658 |
| rs188233184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148023979 | TTCTCACGTCCCTTC[C/T]GAGCCATGCTGTTCA | 79658 |
| rs188274615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147872770 | TGGATCATCATAAAG[A/G]CCTTCATGTGTGTCT | 79658 |
| rs188287219 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147733304 | ATTCATGCAGAAATA[A/C]TGAGTTAGTGATGCT | 79658 |
| rs188289347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147751378 | TTGTTGTTTTTTTTT[C/T]TTTGAGACAGAGTCT | 79658 |
| rs188291720 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147756500 | TATCCGTGGTTTCAG[C/T]TACCCATGATCTGAA | 79658 |
| rs188298649 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147766935 | CTCACTGCATCCTCC[A/G]CCTCCCAGATTCAAG | 79658 |
| rs188307399 | snp | C/T | 0.229136 | 0.249128 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911595 | TCTTGATCTCCTGAC[C/T]TCGTGATCCGCCCAC | 79658 |
| rs188326584 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147946805 | AATAGTTAAATTAAG[C/G]CTTATTTTAAAAAGG | 79658 |
| rs188362868 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147788670 | AGAATTTGCACAGTG[C/G]GTTATAAACAGTCTG | 79658 |
| rs188368619 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148004101 | AGGTCCAGTGGTGCA[C/T]GCCTGTAATTCCAGC | 79658 |
| rs188370881 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147754677 | ATTTTACTGTTACAC[A/G]TGTGCATTAGCACTG | 79658 |
| rs188374268 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147826893 | TCCCTCCCCAAGCCC[C/T]GCCCTCAATAACAGT | 79658 |
| rs188388223 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148038640 | TTGGGCAGAGAAGCC[A/C]CTGAAATACTCAAAG | 79658 |
| rs188399763 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147806223 | TTCCAGGTCGGATCA[A/C]ATTTACTCTAAATTT | 79658 |
| rs188425737 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147736591 | ACACTACTGCTGGTT[C/G]AGCCAACATTCCTTT | 79658 |
| rs188432593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147772378 | GCCTTTCTCCTCTCT[C/T]CTCTCTGCAGTTTTT | 79658 |
| rs188433288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147829843 | TCATTGAGTTTCATC[C/T]CTAGCCTAAAATGGT | 79658 |
| rs188434640 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147842552 | GTGATCCTCTCTGAT[A/T]TCCTCATCTGCTTTA | 79658 |
| rs188437265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147812828 | CTGTGCCCCTTCTTA[C/T]GCTTGTCTCTAAAAT | 79658 |
| rs188438534 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147786512 | TCTTTCCCTTAACCC[A/G]GATACTTTCCCATCT | 79658 |
| rs188440499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147746532 | CAGCCTCCTGAGTAG[C/T]TCGCTTGCCACCACT | 79658 |
| rs188442609 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147825417 | GCGCCATTGCACTCC[A/T]GCCTGGGCGACAGAG | 79658 |
| rs188448968 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147771249 | AAGGAATTCAACATG[A/G]GTACTTGAGGGACAT | 79658 |
| rs188461671 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147792309 | TTGAATATCTTTTCA[A/C]GTATTTATTGGCCTT | 79658 |
| rs188463773 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147912265 | GAAATTCCTTCCAGG[C/T]ACAGTGGCTCACACC | 79658 |
| rs188467701 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147861141 | AGGGCGAGCCAGGCA[C/T]GGAGTGGCGAGGAGT | 79658 |
| rs188467944 | snp | C/G/T | 0.00159649 | 0.0282165 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147866242 | GTAAAGGTTTAATTA[C/G/T]GGGTTTGAGGCTGCC | 79658 |
| rs188468193 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147847969 | AGAAAGAAAAAGTAA[C/T]ATTTGCATGCTGTTG | 79658 |
| rs188475361 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147986022 | TTCCGTTTTCCTGTT[G/T]GAATTAAAGCTCACA | 79658 |
| rs188475557 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148013769 | AAAATAGCATTCACG[G/T]TGGAAATTTCATGAG | 79658 |
| rs188483210 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147961428 | TAGTTCTTTCTAATC[A/T]GATTGCATGCTGTTT | 79658 |
| rs188487463 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147805603 | CGTCATATCCCTTCT[C/T]TTCATTTTTTAAAAA | 79658 |
| rs188495152 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148051230 | GTAGCTCTTACTTAC[C/G]TGTACCCTCAGTAAG | 79658 |
| rs188533904 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147870263 | AGACGGCGATTCACC[A/G]TGTTAGTCAGGATGG | 79658 |
| rs188549350 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147803648 | TCCATGAGGTCAACT[G/T]TATTGGCCCACACAT | 79658 |
| rs188561836 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147943658 | GATTTTTAACAAACC[C/T]ATAAAGTGTCCTTCC | 79658 |
| rs188569934 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147970006 | GGAGGGTTGGAGATG[G/T]GGGATGTCAGTTTGG | 79658 |
| rs188573210 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147884324 | TGCTTACACATACGA[A/G]GGATAATACCTGTAG | 79658 |
| rs188573731 | snp | C/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147738868 | ATTTTGATTGTAGTT[C/T]GGGATGCTGGAAAAT | 79658 |
| rs188574776 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147908778 | CACTCCATAGCTGTA[C/T]GGCTGAGTATTTCAA | 79658 |
| rs188575536 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147767150 | GCCACCGCGCCCAGT[C/G]TACCTGTATGTTAAA | 79658 |
| rs188581543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147840454 | TTAGCATTCTGGTTA[C/T]ATTCCTGCTTTACCC | 79658 |
| rs188583516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147865333 | GTACTTTAAACAATC[A/G]TTTGTAACATGACTT | 79658 |
| rs188583678 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147783778 | ATTATTATATTTATA[A/T]AACACACATTAAATT | 79658 |
| rs188584108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147775164 | GTGATCCACTCGCCT[C/T]GGCCCCCCAAAGTGC | 79658 |
| rs188589299 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147821840 | GCTTTAAACCAGAGG[C/T]AGGATTGTATACTGC | 79658 |
| rs188602817 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147909638 | ATCAAGCTTATAAAA[A/G]TGTATTTTTTTTTGT | 79658 |
| rs188604348 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147809894 | GGGACCCCTGCTATA[C/T]GCCAAGGAGATTTAG | 79658 |
| rs188611638 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147904475 | CCTATGAGTGAGAAC[A/T]TGCAGTGTTTGGTTT | 79658 |
| rs188618842 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147809518 | CAATATTGGTTCTAG[A/C/G]TTGTTGATGAAGAAA | 79658 |
| rs188634765 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147845753 | AAAATGACACAGGTG[C/T]TCATGTAAGTGTGCC | 79658 |
| rs188642582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147926900 | CAAACTAGATAATAG[C/T]GAGGTTGTACTTGTT | 79658 |
| rs188646750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147963320 | CCTTCCCCGTTCTTC[A/G]GGACCCAATCTCCAA | 79658 |
| rs188650314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147944917 | GACTCAGCAGTGGCA[A/G]TAACCTGCTACGTTT | 79658 |
| rs188661360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147980809 | ATTTGTCTACTTCCT[C/T]TAGATTTTCTAATCA | 79658 |
| rs188661660 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147918994 | GGACTCATTTTTCCT[C/T]TTCTACTAAATTCTC | 79658 |
| rs188667356 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148007847 | GCTTGCTGGGTTTCT[G/T]TCTAGTTCCTTCAGT | 79658 |
| rs188675701 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147883320 | TCCCACCTTGGCCTC[C/T]CAAAGTCATAGGACT | 79658 |
| rs188714223 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147983124 | TGGGCTCAGAAGATC[C/T]ACCCGCCTTGGCCTC | 79658 |
| rs188719967 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147947107 | TGACAACATGTCAAT[A/G]CAAAGCTCTTTGAAA | 79658 |
| rs188725590 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147753446 | CCTCCTGGGTTCAAG[C/T]GATTCTCCTGCCTCA | 79658 |
| rs188743204 | snp | A/T | 0.0696718 | 0.173152 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147936498 | CGTGCCCGGCTAATT[A/T]TTTTGTATTTTTAGT | 79658 |
| rs188751047 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148010015 | TTGAAATTAAATTTC[C/T]TATAGTTAACTAATC | 79658 |
| rs188752801 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147953194 | AGAATAGTTGCATCT[A/T]TGTTCATGAGTGATA | 79658 |
| rs188758794 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148047908 | GTTCACTGCAACCTC[C/T]GCCTCCTGGGTTTAA | 79658 |
| rs188765566 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147916921 | ATTCTTTGCTTGCCC[C/G]TACATCTGCCTCCCA | 79658 |
| rs188771756 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147971483 | CGGAGACTTCAGAGG[A/C]GAGTTTATGTTCAGC | 79658 |
| rs188774768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147860743 | ATTTCCTAAATAACT[C/T]TATGTGAGACTTGTC | 79658 |
| rs188789048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147785776 | CAATTATTTCATATA[A/G]GGAAGATTGTACTCT | 79658 |
| rs188794437 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147825163 | ATTTAAAAAGTGACA[C/G]AGGGCTGGGCGCAGT | 79658 |
| rs188795930 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148000627 | TGCCATTCTAACTGG[C/T]GTGAGATGGTATCTC | 79658 |
| rs188803751 | snp | C/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148029980 | TCCCCAGAAACCTCC[C/T]GTGAGGCTCAGCATC | 79658 |
| rs188805113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147898596 | TTCTGTTTATTTTTT[A/G]GGATTCGAATTACCT | 79658 |
| rs188805844 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148012283 | TGCTTTTGAGACATG[C/G]CTGCTATGTCTGAGA | 79658 |
| rs188815631 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147887256 | CACCCTGCCTTTCCT[C/T]CCTGCCTGTGGGAGC | 79658 |
| rs188821935 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147924734 | TCTCAGTTTTACTCC[G/T]TATTAACTCTGCCTG | 79658 |
| rs188822461 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148049937 | TGGTGGCATGATCTC[A/G]GCTCACTGCAACCTC | 79658 |
| rs188830250 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148067767 | CGTCAGTAGTTATGC[A/G]TTTGGGATGTGTGCA | 79658 |
| rs188837771 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147926354 | AATATTTGCAGTGGA[A/G]AGAAGGGATGGATAG | 79658 |
| rs188847191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147994566 | TGTTCATATAAAGAA[A/G]CAGTTGACATCAGAA | 79658 |
| rs188890515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148052176 | AGAAATTACAGGGTG[A/G]GAGTCACTGGCAAAC | 79658 |
| rs188908322 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147863892 | TCAGTTTCTTGACAT[A/C]CTCACCAACACCACT | 79658 |
| rs188913387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147751618 | TGATGTGCCTACCTC[C/T]GGCCCCCTAAAGTAC | 79658 |
| rs188935289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147903939 | CATCCATGTGCAGGT[C/T]CTTGTGTAGACATAG | 79658 |
| rs188940167 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148008341 | GGTGCTAACAGTTAC[A/T]GAATTAGAGCTCTGA | 79658 |
| rs188942337 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147997876 | ATAATAGGAGCAAAA[A/T]AATTAGTCCCAGTAA | 79658 |
| rs188949540 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148059790 | GGCGTGGGACTCGCG[C/G]TCAGAGCCAACAGCC | 79658 |
| rs188950567 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148026144 | CAGAGATTTGGTATT[G/T]GAGTGAAGTGGTTTG | 79658 |
| rs188962966 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148045687 | AGCTTGCGGTGAGCC[A/G]AGATCGCGCCATTGC | 79658 |
| rs188978261 | snp | C/T | 1.64857e-05 | 0.00287099 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148064469 | AAGCAGAACACAGCT[C/T]GGAATTATCTTTTGA | 79658 |
| rs189000319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147966038 | TGAGAACAGTTGTCT[A/G]TGTGATTCACTGCAC | 79658 |
| rs189009593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148000137 | GTGTCCAAGTGTTCT[C/T]ATTGTTCAATTCCTG | 79658 |
| rs189012867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147941323 | AGTGCTAAGCTGTCT[C/T]AAAATTTGTTGGTCA | 79658 |
| rs189017227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147977094 | AGCATCTGGAGATGC[A/G]GAGCTGCAAAGAGAG | 79658 |
| rs189028631 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148005195 | CCCAGTGTCTATAAC[A/G]CTGCATGTCCCATAT | 79658 |
| rs189033862 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147936938 | CGCCTCCTGTCAGAT[C/G]AGTGGCGACATTAGA | 79658 |
| rs189037660 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148029203 | AGAACAGTCCTATAA[C/T]TATGAGCAAAGTACA | 79658 |
| rs189045722 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148066870 | TATAGACGTATGGGG[G/T]AGAGGCTGCTGACCA | 79658 |
| rs189048773 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148039615 | TAGGATACTACTTCA[A/G]TTTCCTTCTGCACTT | 79658 |
| rs189062083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147907619 | TGTGGTAACAGAGAG[C/T]GCATTGGTGAGTGTA | 79658 |
| rs189072099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147842296 | GCTCAGACGGATATT[A/G]CATTGAATTCTCCAA | 79658 |
| rs189082268 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147942615 | CCTTTGTTCCCTCCT[G/T]ATCCTCTTTATTCTC | 79658 |
| rs189085285 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147843108 | ACAAACCCGTTTGTA[C/G]TGGGCACCCCTTTTC | 79658 |
| rs189102548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147878682 | CTGTTGATTTTTCTA[A/G]CAAACTATTTAAACA | 79658 |
| rs189110539 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147978659 | TGAGGCCTCCCAGCC[A/C/G]TGCTTCATGTACAGC | 79658 |
| rs189115815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147880397 | CAGACATGGAAAATT[A/G]GTCATGGTGAGGAGA | 79658 |
| rs189117517 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147901691 | TGAAGCCTGATAATT[A/G]CTTTTTCCCTTACTT | 79658 |
| rs189131567 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147861415 | GGCTCCCCGAAGGGC[C/T]GCAGCTCTTCTCTCC | 79658 |
| rs189139044 | snp | A/T | 0.0528381 | 0.153711 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147762540 | TTTATTTATTTATTT[A/T]TTTTTTTTGAGACGG | 79658 |
| rs189174653 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147796817 | GGCGTGAGCCACTGC[A/G]CCCGGCCTGTTCCTT | 79658 |
| rs189184744 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148071590 | CACCGCACTCCAGCC[C/T]GGGCGACAGAGCGAG | 79658 |
| rs189206193 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147816505 | CATTACACAGACACC[C/G]CAGGCAAGCTGGACT | 79658 |
| rs189209671 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147761853 | CGAAGGAGAAAAAGT[G/T]AAGTGAATTAAATGA | 79658 |
| rs189213749 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147779001 | TGACGTGGGAATAGC[A/G]AATATGTGTTTGGTA | 79658 |
| rs189260991 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147922987 | TTTCTAAATACAGGC[A/T]TGCCTTGCACACATA | 79658 |
| rs189277162 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147933506 | GCCTTCCAGGATTCT[A/G]AGATGACTGACTCTT | 79658 |
| rs189283222 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147948773 | CATCCTTGCTAACAC[A/G]GTGAAACCCCGTCTC | 79658 |
| rs189289175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147914220 | GATTTCAGCTGTACA[A/G]ATGGAAGAGTTTTGA | 79658 |
| rs189289404 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147992986 | GTCTTTCAGGACATT[A/G]TTAGTCATTAGTCAT | 79658 |
| rs189293574 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147957669 | TCTGTTCTGTGGTGA[A/T]GAGATAGTTTCTTCT | 79658 |
| rs189297187 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147975844 | CCAGAATAATGTTAC[A/G]TGCACATATAGAGGA | 79658 |
| rs189301208 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148004510 | GTAAATCTTTTATTA[C/T]ATAAGATTGTCTTAG | 79658 |
| rs189304698 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147803172 | CACCACAATGCCAAG[A/C]TGATTTTTGTAATTT | 79658 |
| rs189306286 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147957962 | AGAGAGTTAATGTAA[C/T]TTTCTCCGTTAGCTG | 79658 |
| rs189313800 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147993700 | CAATTTAAAGACTTC[A/G]TGTACTAAGCATTTA | 79658 |
| rs189321139 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147791734 | AGATTATAGGCACCC[A/G]CCACCATGTCCAGCT | 79658 |
| rs189321754 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148020381 | TGCTGGTTTGCTGCA[C/T]GTATCAACCCATCAC | 79658 |
| rs189321933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148021335 | AGTTTTCAGCATTTG[C/T]GCTGTTCCAGTCAGT | 79658 |
| rs189334544 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147838733 | GAGATGGGGTTTATG[C/T]CTTGTTGCCCAGGCT | 79658 |
| rs189349156 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147740707 | CTCTTTTCCTCCCCA[G/T]TCCTTGTCCTACCCT | 79658 |
| rs189350948 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147759278 | TTACTCTTAGAGAAA[C/G]AGAGGCTCAGAGGTG | 79658 |
| rs189355879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147811926 | CAAGGGAGGGTGTAA[A/G]CAAGGTGGGGGATAC | 79658 |
| rs189364511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147776850 | AGCAAAATGCAGTTC[A/G]TCCAGATGCTGTGAA | 79658 |
| rs189367664 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147874233 | CAGTTTCACATCAGC[A/G]GTTTTTTGGTATTAA | 79658 |
| rs189418434 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147746195 | TGCATCCTCTGCCTC[C/T]GGGGTTAAAGCGATT | 79658 |
| rs189426213 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147780714 | TAACAAGCCTGCCTC[A/G]TCTTGTGGGTGGTAT | 79658 |
| rs189439444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147954124 | CCCAGAATATGGTTA[A/G]TCTTGGAAAATAAAT | 79658 |
| rs189439569 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147989581 | AGAAAAAGAATTCAG[C/T]GATATTTCTCCCATT | 79658 |
| rs189445894 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147972207 | AAGACATGAGATTGG[C/T]GTAAGAAAATATTTA | 79658 |
| rs189446709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147817347 | GTAGGGTGACCCAAA[C/T]AGAGATGCTCCCCAT | 79658 |
| rs189457868 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148003002 | GTTCTTTTAATTGTG[A/G]TGTTAGGGTGTTAAT | 79658 |
| rs189460101 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148063845 | TTTCCATGAACGGAC[A/C]CAGAGGTTGCTTTAA | 79658 |
| rs189465580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148016309 | AGGAGTTTGAGATTA[A/G]CCTGGGTAACAAAAC | 79658 |
| rs189466247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148025416 | TCTTAAGTTTGGTCA[C/T]AGTGATTTAATCTTA | 79658 |
| rs189467540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148034700 | GACAGGTGAAAAGCA[A/G]GGAGTCTGGCAATCC | 79658 |
| rs189474255 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147817116 | TTGTATTCAGATTTA[A/G]TGAGTGACAAGAGTA | 79658 |
| rs189481108 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148064170 | GGAGGAGAATTAGGT[C/G]AAGTGGTTCAGTGAC | 79658 |
| rs189481706 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147852876 | GACATGCGCCAGCAC[A/G]CCAGGCTAATTTTGT | 79658 |
| rs189481956 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148056316 | TTCACACATCTCTTC[A/T]TGTCATTAAACCAAC | 79658 |
| rs189485787 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147879496 | TGAGTGAAATGGGCC[A/G]GAAGACAGAACAATA | 79658 |
| rs189492498 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147870435 | TAAATATTTTGGTCA[A/T]CTTTTAAGTATTTAA | 79658 |
| rs189500968 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147798726 | AGGAGTTTGAGACAC[A/T]CTCTCTCTCTCTCTC | 79658 |
| rs189501942 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147952918 | TGTGATCCATTTTGA[A/G]TTAATTTTTACATAA | 79658 |
| rs189507076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147851555 | CCAAAGATTCTATAA[A/G]TTACTACAAAACATG | 79658 |
| rs189512866 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147916217 | ATATGATTATCTAAA[A/C]ACTAGTATTTCATAT | 79658 |
| rs189514380 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147833806 | TTAGATTCAATGATA[C/T]ATATATTAAGTTGGT | 79658 |
| rs189518876 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889922 | TTATTTTTTTCTCTT[A/G]TTTGGGAAGCCCAGA | 79658 |
| rs189522378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147926745 | CAGAGGGATAGGAGG[C/T]GAAGGAAGAAGGATG | 79658 |
| rs189535937 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147908966 | CTGAGAAAACACAGC[A/G]CACTATCTGCCTGAA | 79658 |
| rs189546992 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147886847 | ACCATCTCTGCTCAC[C/T]GCAACCTCCGCCTCC | 79658 |
| rs189548994 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147933991 | GGAAGCCTCAGGCTC[C/T]CAGGCTGCGAGACAT | 79658 |
| rs189552999 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147907721 | TAAATTAACATAGTA[C/T]AAAAATTGATGCTAT | 79658 |
| rs189566626 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147783538 | ACATTAAATTATGTA[C/T]TGTATAATTTATAGA | 79658 |
| rs189569732 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147967533 | GGGTGAGCAGAAACT[A/G]CTTTAATATACTCTT | 79658 |
| rs189580209 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147949077 | GGTTGTCCCACTTTT[A/T]AATGATATAAAATTT | 79658 |
| rs189583544 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147829108 | CCAGGCTGGAGTGCA[C/G]TGGTGTGATCTCAGC | 79658 |
| rs189585255 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147985086 | GCCTAATCTCATCCA[A/G]GAGAGTGGGTCCTCC | 79658 |
| rs189599336 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148013273 | ATGTAAGTCATTCCT[A/G]TAAACGTGTACTTGG | 79658 |
| rs189599535 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148000828 | ATTCTGGATATTAGC[C/T]CTTTGTCAGATGAGT | 79658 |
| rs189606453 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148031197 | AGAGAAATAGTGATT[A/T]TTTAAGTCTGTTTAT | 79658 |
| rs189615091 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147856422 | TGGTAGACAATCTTA[C/T]TGCTATACAGGTCGA | 79658 |
| rs189619036 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148050496 | CTCCTGCCTCAGCCT[A/C]CCGAGTGGCTGGTTC | 79658 |
| rs189630824 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147820516 | GTCTCCACCTCCTGA[A/C]CTCAGGTGATCCACC | 79658 |
| rs189633411 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147895069 | ATATTGTGAATATAG[A/T]ACCTTACAGTTCATG | 79658 |
| rs189652090 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147894166 | ATTGCTGGGGTATGG[C/T]ATATGTATGTTTGAC | 79658 |
| rs189669789 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147737082 | TCTTGTTAAATGACA[C/T]AAGACAGTTTTGAGT | 79658 |
| rs189677157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147932655 | GACCTGTCAGAAGGC[A/G]GGGGTGGGAGGAGGG | 79658 |
| rs189703868 | snp | G/T | 0.00194317 | 0.0311096 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147966656 | CTTTGGTTAAACAGA[G/T]TCCTCCCCCCTTACC | 79658 |
| rs189710871 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147799128 | CAACCTCTGCCTCCC[A/G]GGTTCAAGCGATTCT | 79658 |
| rs189716753 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147965218 | CGGGTGGAACTGGGG[A/G]CCACACCTGGAAGGG | 79658 |
| rs189731098 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147982428 | AGGCTGGAGTGCAGT[C/G]GTGCAATCACGGCTC | 79658 |
| rs189739489 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148009010 | TTTAGTATTAAATAA[A/T]ACATATATTTAAAAG | 79658 |
| rs189741552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148035021 | TTACTTGCTTTATAA[C/T]TGAATTGCTGCAGAT | 79658 |
| rs189746634 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147762731 | AGAGATGGGTTTCAC[C/T]GTGCTAGCCAGGCTG | 79658 |
| rs189748036 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148056623 | AAATAATGAAATTAG[C/T]GTTGATACAGTACTG | 79658 |
| rs189748142 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147999389 | TTGCAACTACACACT[C/T]TTCTGGTCCGTGTTT | 79658 |
| rs189748549 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147899474 | ACAATGGTTTCATAG[G/T]TTCTCCGTCTTGTTC | 79658 |
| rs189749122 | snp | A/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148021858 | ATAAATTAAATTTTC[A/T]CTAGCACATATTTGT | 79658 |
| rs189752606 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147871115 | CAGGTGCCCGCCACC[A/G]TGCCCGGCTAATTTT | 79658 |
| rs189757296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148061370 | TGGCAATTGTTTGGC[C/T]AACTGTGGCCTTAAT | 79658 |
| rs189761863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148027756 | TGATATAAATTAGCC[A/G]TCTTAGGTAGGTTGA | 79658 |
| rs189763196 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147834273 | CAGGAGTTCAAAACC[A/T]GTCTGGGCAACATAA | 79658 |
| rs189806097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147971135 | TCCTGGGCCAAAATA[C/T]TATTAAGGTCTTTCT | 79658 |
| rs189816412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147738247 | CTATATCTGTGTTCT[C/T]GTCAGTAAAATAGAA | 79658 |
| rs189845533 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147981016 | TTTCAGAGAACCAAC[A/T]TTTCATTTTATTGAT | 79658 |
| rs189849525 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148002750 | TATTTCTGTGGGATC[A/G]GTGGTGATATCCTCT | 79658 |
| rs189849714 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147846952 | TCTGCCCACCTCCTC[G/T]TCCCTGAAAATATTT | 79658 |
| rs189854249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148034062 | CTAAGCCTCACAAAT[C/T]TGGACAATAAAACTT | 79658 |
| rs189861831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147810535 | TCTGAACGTTTACAT[C/T]TCATCTTTAATACAA | 79658 |
| rs189871648 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | ARHGAP10 | GRCh38.p7 | 4:148073006 | CACACCTCCTCCAGT[A/G]GCTGCACAGGCCTCT | 79658 |
| rs189907043 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147875510 | TTCTCCTTCCCCCTC[A/G]CCTCTACCCTCATCA | 79658 |
| rs189942485 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147733455 | CCATACAGCAGACAG[A/G]GACTTGGGCAGTATC | 79658 |
| rs189949720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147984218 | GGGAATGGGCAGAGG[A/G]AGGCAACAGAGAAGC | 79658 |
| rs189959518 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147790805 | AGTACATAGAGAATA[C/G]TATACTGAATACTTC | 79658 |
| rs189970453 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147735636 | CTTTTCAGCAGAAGG[C/T]TGACATAATAGCAAA | 79658 |
| rs189989151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148012975 | GTTTTGTGTTTGCCA[A/G]CATTTCTACAAGGAA | 79658 |
| rs189991860 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148005958 | TCTTAGTGCAGATTA[A/G]AAGTAGCCACAAATT | 79658 |
| rs190002299 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148040090 | TTTCACTGTCTGGCT[A/G]TTGCCTCCACTGGGG | 79658 |
| rs190024967 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147752715 | GTATTTTAGTAGAGA[C/T]GGAGTTTTGCCATGT | 79658 |
| rs190035771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147768770 | TTGGCAGGGAATCTT[A/G]CTCTGTCACCCAGAC | 79658 |
| rs190081602 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147930113 | ATATTGATGAAGCAT[C/T]TCATTCCATGCCAGG | 79658 |
| rs190081964 | snp | A/C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147964023 | ATCGTGTATTAAGCA[A/C/T]GCCTTTTTATTCTGA | 79658 |
| rs190086744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147988111 | CTGCAGGTGTCTCCT[A/G]CCTGTCCCTGAGGCT | 79658 |
| rs190093599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147946349 | ATTGTGGATGTTGAA[A/G]TAATATACTATGTCT | 79658 |
| rs190095338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148015139 | CAGGACTCCAAACAG[A/G]GCCCTTCATTTGCTC | 79658 |
| rs190098357 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147773396 | TTTTGTGCTAATAAA[C/T]AAACATCCCTTGGAA | 79658 |
| rs190112573 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147833161 | ACAGAGGAAAAATAT[A/G]TGTGGTGATACGGTT | 79658 |
| rs190116101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147774686 | ATAGTATAAAATTCA[A/G]ATAATGCTTTTACCT | 79658 |
| rs190125132 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148054764 | ACCTACTGAGACCCA[A/G]CCACATTTATAACTT | 79658 |
| rs190134697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147742301 | TAAGAACTCTGCCTC[A/G]CTGGTGGTGGTATTT | 79658 |
| rs190135775 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147737849 | TTTAGAGTTGTTCCT[A/G]TTTAGAGCTTCCCAC | 79658 |
| rs190147372 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147826600 | AAATTTCAAACATGT[A/G]CCAAAGTCGAGAGAA | 79658 |
| rs190158176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147809305 | CCTCTATCTGCAGCC[A/G]TTTGTGGAATTTGTG | 79658 |
| rs190158559 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147808159 | TTATATACAACTAAC[A/G]ACTGTGGGACCCCAG | 79658 |
| rs190176492 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147882056 | TCTTGCTATATTTCC[A/T]GGCTGTGTGTTCATT | 79658 |
| rs190178259 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147788533 | TGTCCAGTCCTTGGT[G/T]AGATTAGGGGTGAGA | 79658 |
| rs190180343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147862571 | CTGCTCCAGACTGGC[C/T]GCTGCTGCCATCATT | 79658 |
| rs190186682 | snp | A/G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147844310 | ATAGGGTATCCATCC[A/G/T]TTCAAGCATTTATCC | 79658 |
| rs190204060 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147776567 | CAATGTGAAGCATAT[A/T]TCTCCCTTCAGAGAC | 79658 |
| rs190221210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147902564 | TGGCCAACATGGAGA[A/G]GCCCTGTCTCTACTA | 79658 |
| rs190238822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147740128 | ATCTTGGCTCACTGC[A/G]ACCTCCGCCTCCCAG | 79658 |
| rs190261336 | snp | A/C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148030512 | GGAGAAGGTATTTCT[A/C/T]TGTGTAACCAATTCC | 79658 |
| rs190265517 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147783164 | ATTATATATTGTATA[A/C]TTTATATAACACATT | 79658 |
| rs190265822 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147769216 | AGTGAAATTACTCAG[C/T]AAATGTTGAAGAAGA | 79658 |
| rs190274745 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148068503 | AATCTGAGAAAAAAA[A/T]ATCGAGTGAAAAAAT | 79658 |
| rs190285691 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148032468 | TTAGCAAGTCTGTAC[A/C]TTGTGAAACTGCTGT | 79658 |
| rs190289695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148050903 | TAACCAAAGTTGCTA[C/T]GGAGTCATTGAAACT | 79658 |
| rs190293751 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148070164 | CAGTGTGTCTCTCCT[A/G]TATATACACGTATGC | 79658 |
| rs190295705 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147884599 | AACTCCTGGCAGGGG[A/G]ACCTAATCTAGTTTA | 79658 |
| rs190296707 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147824012 | TCTCACCATTTATTT[C/G]AGGCTTAAAAAAAAA | 79658 |
| rs190307358 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147805165 | ATATGGAGTTAGGAA[G/T]GGGGTCTAGTTTCAG | 79658 |
| rs190310029 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147847475 | TAAAAATACCTGTAA[A/C]CAAACAACACATTTG | 79658 |
| rs190316328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147921974 | GAGTCATCTGCTCTG[C/T]CCACATCTCTGGAAA | 79658 |
| rs190321890 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147785205 | AATGTTCAGGCATCA[A/C]TAAATCTAAAAATAA | 79658 |
| rs190322080 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147877779 | TGGGGCATACTTGGA[C/G]AGTCACTCCTATTGA | 79658 |
| rs190325943 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147906483 | TAATGCCATTGAACT[C/T]TACACTTAAAAATCG | 79658 |
| rs190328051 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147859509 | GAACTCCTGACCTCA[A/G]GCGATCCACCCACCT | 79658 |
| rs190330317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147923510 | CTTAAAAAATCTTCC[A/G]TATGTGGATAATTTG | 79658 |
| rs190332280 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147886067 | TACCTACAGGCTACA[G/T]GTATAAGGGGTATAT | 79658 |
| rs190338597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147841871 | GCCACAACTACTACT[A/G]TCCTTGTTTTGGAAA | 79658 |
| rs190342863 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147755720 | TGCCCTTATATAGTG[A/T]AGGTGATATTTTTCT | 79658 |
| rs190346832 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147958638 | GCTTGATGTATTCAT[G/T]TCACGGTAGATACGA | 79658 |
| rs190357015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147977691 | GATTTGGGGGTACAT[A/G]TACAGGTTTGTTACA | 79658 |
| rs190358529 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147786930 | GGTCACACCTCTGAC[A/C]TCCCTGGACTCAGTT | 79658 |
| rs190365604 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147941990 | CTTCCAAAAAAAGGG[C/T]TTTAGAGTTTTGAAT | 79658 |
| rs190373859 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147994381 | AAAGTTCTTGTTAAT[A/C]CTTGCACAGCTGGTG | 79658 |
| rs190385730 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147984578 | ACTGGCAAGGTGTCT[A/G]TTTGAGTTCTGTGGT | 79658 |
| rs190397823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147825715 | CATCACCTTTCTAGT[A/G]CATGGAGCCGATGTG | 79658 |
| rs190401994 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147850930 | ACTTAGGGGCCAAGT[A/G]TGTTGAACAAAAACT | 79658 |
| rs190439396 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147732818 | TGCTGCCTAAAGCTA[C/T]TCACAATCTCTTACA | 79658 |
| rs190443231 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148066774 | AGCTGATTCTTCATC[A/C]TAAGCGGCAGGGATG | 79658 |
| rs190454159 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147766526 | GCAGAACTCATGGAT[A/G]TGGAGGGCTGTCTGT | 79658 |
| rs190454260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147861614 | TGAGCAACAGAACAG[C/T]TCTCAGGAGACCTGA | 79658 |
| rs190462857 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147961892 | CCACCTCTTCCTCCT[C/G]CTTGGCTGCATTGCC | 79658 |
| rs190470387 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147937648 | CAATAGCAAAGACAT[A/G]GACTCAGCCTAAATG | 79658 |
| rs190477352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147902154 | TGTAGAAGCACTTCT[A/G]GAATATTTCCCAAGC | 79658 |
| rs190477890 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147918618 | GGCCATCCCTGGTCT[A/G]GACTTAGGGGCCCTT | 79658 |
| rs190480208 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147882881 | CTTTTTAATGGCTGA[A/C]AGTACAGTGATTCCT | 79658 |
| rs190486099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147903495 | CATAGTTTACATTAG[A/G]GCTCACTCTTGGATT | 79658 |
| rs190491236 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147955085 | TGAAATACTGTATGC[G/T]TAGGTCTAGTAGGGA | 79658 |
| rs190494478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147996934 | CCCTGCCAGCACCAT[A/G]GTCTTGGACTTGCAG | 79658 |
| rs190498745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147802305 | ATAGGTGATCCATAG[A/G]CTAAAATGAGATGTT | 79658 |
| rs190503631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147973527 | ATTTATCCATTCTTT[A/G]TGTTACAAGCAATCC | 79658 |
| rs190504285 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148024677 | CAATTAAGCTATAAT[A/T]TCAGAACTTCCTTTT | 79658 |
| rs190505600 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147938231 | TGGAGGGTGGGAAAA[A/G]GGAGGGGATCAGGAA | 79658 |
| rs190513443 | snp | A/G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147829481 | GATGTGAGCCACCGC[A/G/T]CCCGGCCAGGACAGT | 79658 |
| rs190522134 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147990611 | GAGTACTAAAAAGAA[C/G]AAGATCATGTCCTTT | 79658 |
| rs190543039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147865926 | TCTAAGTGTTGTACC[A/G]AACTCATTATTCCAC | 79658 |
| rs190571628 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147941082 | ATTTAATGGGAGTAC[A/G]GCATCTGCTTTTACT | 79658 |
| rs190596013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147877040 | ATCATTAGTGTGTAT[A/G]CCCAGAGCTGGTTGA | 79658 |
| rs190606132 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | ARHGAP10 | GRCh38.p7 | 4:147730123 | CATCCATTACACAGC[C/T]GACAAAGGACATTTT | 79658 |
| rs190611679 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147747090 | ATACCCAGAAAGGCC[A/G]CTGTTTCAGGCTTTA | 79658 |
| rs190620812 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147966900 | CCATGTACTACACAA[C/T]GATCCTCTTAGATTT | 79658 |
| rs190630508 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148000757 | TTCGTATCCTTCGCC[C/T]GCTTTGTGATGGGGT | 79658 |
| rs190633324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147915023 | TTAATTCACTCTCAT[A/G]TATTCTGTATTCCAG | 79658 |
| rs190639591 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147942745 | GAGGCCAGGTAAAGG[A/T]GCAGGCAGCTGCCTT | 79658 |
| rs190646069 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147978227 | TGGTAGTTCTATTTT[C/T]AGTTCTTTGAGAAAT | 79658 |
| rs190654366 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148006285 | GCTTTCCTGTCCAGG[C/T]ACTGGACATGTGAAG | 79658 |
| rs190660046 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147978825 | TAATGATGTTGAACA[A/T]TTTTTTCATATGTTT | 79658 |
| rs190660298 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147994454 | TGCACATGGGCTACA[C/G]ATTTTAGCCTGTGCC | 79658 |
| rs190664734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147779945 | CCCTTATAGTCTTGC[C/T]CGAGTATGAGTGGGA | 79658 |
| rs190673212 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148022207 | ATAGATGTGCAGAAC[A/G]TGCAGATTTGTTACA | 79658 |
| rs190673436 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147763617 | GCCTGGCCTGGCCTG[A/G]CCTGGCTGAGTGATT | 79658 |
| rs190679208 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148040404 | TGGAGTACAGTCATG[C/T]GATCTCAGCTCACTG | 79658 |
| rs190681323 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148061927 | CTTCAGGGAAGGTGT[A/G]TGGGTTAGAGAGGCC | 79658 |
| rs190684412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147781069 | ACCTAACCTAGGACT[A/G]CTGGCGGGGCCGGGC | 79658 |
| rs190685097 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147881445 | GAGATTGACACCAGC[A/C]TGGCCAACATGGTGA | 79658 |
| rs190688276 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147835133 | AGTGCCTACTATGAG[C/G]CACCGTGTTCTCACA | 79658 |
| rs190689843 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148006899 | CCCCATCAGCCCACC[C/T]CAGCACACATGCTTT | 79658 |
| rs190692331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147800074 | GGTGTTTGTCTGCTT[A/G]GTGGTTAGATGCCGC | 79658 |
| rs190692539 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147818303 | GGGCGCGGTGGCTCA[C/G]GCTTGTAATCCCATC | 79658 |
| rs190699510 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148069339 | GGATCCCCCTTGGTC[A/G]CCTCTGTAAAGCAGT | 79658 |
| rs190706461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147844073 | TACTAAGATCTTGGG[C/T]GTTTCTCAGCATCTG | 79658 |
| rs190707681 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148040821 | AAAAGATTTGGGGGG[G/T]GTTATTTGGTGTATG | 79658 |
| rs190724990 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147980096 | TGGTGAGAGTGGACA[C/G]CCTTGTCTAGTTCCG | 79658 |
| rs190728557 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147944423 | CAGACCTTTGAGTAA[A/T]TGACCTCATATGTAT | 79658 |
| rs190730623 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147917348 | TTCAAGATACGATAA[A/G]CAGACAACACATGTA | 79658 |
| rs190755270 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148007426 | GAGGAAGAAGAGTGT[C/G]ACAGGTCAGCTTGAC | 79658 |
| rs190759112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147743178 | AGCTGGGATTACAGG[C/T]GTGCACCACCATGCC | 79658 |
| rs190767035 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147760938 | AGGCTGAGTGTGAAA[C/T]TAATAGCTCTCAACT | 79658 |
| rs190771992 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148043115 | CCAGTATATGATGGC[A/G]AAATGCAAAATTGAT | 79658 |
| rs190790930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147990300 | TCTTTGGAATGGCAA[A/G]CAGTAACATCCTACC | 79658 |
| rs190804031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148016610 | AGATGTGTGGGGGTT[C/T]TTCCTACACACCAAG | 79658 |
| rs190825346 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147777984 | ACTGTTCATTAGTCT[A/G]TGCATGGCACTCAAC | 79658 |
| rs190827640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147895405 | GGCCAGGCATGGTGG[C/T]TGACACCTGTAATCC | 79658 |
| rs190831462 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147831454 | TAGTTTCATCTTATT[A/G]TATTTACAGTATTTT | 79658 |
| rs190834016 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148046621 | AGGAAGTCATTGTGG[C/T]TGCCATTATGCCTTT | 79658 |
| rs190835472 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147793166 | TGTGTGTGTATGTAT[A/G]TGTGTGTGTGTGTGC | 79658 |
| rs190835867 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147876140 | TCTATGCAGGCAGCA[C/G]GATGGTTGTGCCTTT | 79658 |
| rs190837806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147858144 | TCATTTATTTTGGAG[A/G]CAGCCATATGTAAGC | 79658 |
| rs190843615 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147813722 | CATAGCTGTACTGTG[A/C]GTTTTTTCTCAAAGC | 79658 |
| rs190848785 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147858853 | CTTCACTTTCTCATT[A/T]GGTATTTCATTTTAA | 79658 |
| rs190878725 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147896257 | TCCCTTCTTCACTGT[C/T]TTTTCATAAATGTGT | 79658 |
| rs190889465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147741698 | CTTTATAAACACATA[C/T]ACACACACACAGAGA | 79658 |
| rs190900980 | snp | C/G/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147777169 | GCTATGTATCTCTGG[C/G/T]CTTTTACCATTAGGA | 79658 |
| rs190923630 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147960204 | ACAGTTGTGTTTTTG[G/T]TTCTGGTGATAAATT | 79658 |
| rs190930286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147995585 | TTTTAAGATGACAGA[A/G]TAAAGACAGATTTGT | 79658 |
| rs190936896 | snp | A/G | 1.65784e-05 | 0.00287905 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148023411 | GTCTGGAGCTGGAAG[A/G]TGGTAAGATGTTAAT | 79658 |
| rs190947641 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147835749 | CTGTGCCACTGAGTC[A/G]TACCATTCACTTCAG | 79658 |
| rs190953786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147841512 | ATTTGGTATTCATTT[A/G]TTGCTGGGGAAGAAG | 79658 |
| rs190958467 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147818790 | AGACATCTATAAAAT[A/G]TGAACTGCATGGGAA | 79658 |
| rs190963650 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148062596 | TTTAAAAAAAAAGGG[A/C]AATATTAAGAAATGC | 79658 |
| rs190965864 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147890671 | ATCTCTACTAAAAAT[A/G]CAAAAATTAACTGGG | 79658 |
| rs190973611 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147804755 | TGCTGAGCTTTTTTT[C/T]ATATGATTGTTGGCC | 79658 |
| rs190981237 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147871768 | TCTATTGATTTTATG[A/C]AAAGTTTTCAATTCA | 79658 |
| rs190986250 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147854055 | TTGAATTGGGGTTCT[G/T]AGGTTCTTCTCTTCT | 79658 |
| rs190995195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147945958 | GAAGAGGTCTGGCTC[C/T]TCCTTTGCATAAGGC | 79658 |
| rs191004013 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911545 | TTTATTGTATTTTTA[A/G]TAGAGACGGGGTTTC | 79658 |
| rs191010145 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147929331 | TATGATGGTGAATAT[C/G]TCCCTTTGATGGAAT | 79658 |
| rs191035453 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148003101 | ATGTGTCCCAGAGAT[A/T]CTGGTATGCTGTGTC | 79658 |
| rs191037061 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147787470 | TGGGGGAGGAGGCTC[A/G]CAAATGTGTTCTTGC | 79658 |
| rs191046712 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147756012 | TTCTGTCACATAATA[A/T]GTCAATAGTAGGTGG | 79658 |
| rs191070501 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147755886 | TGTATTATTTCACAT[A/G]TGTGTTGAGGAGCAA | 79658 |
| rs191078697 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147773891 | TCTTTAGTCCTTGAT[C/T]TGTTGTCAAGTGAAG | 79658 |
| rs191087001 | snp | A/G | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148066162 | TTCCCTGGCGGGAGC[A/G]AGATGACTACCACAG | 79658 |
| rs191090473 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147806198 | CTCAGTGTCCAGAGT[C/T]CAGGCGGCTTTCCAG | 79658 |
| rs191090896 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147850107 | TGTCTAGCCAAAGGT[C/T]TGTAAATGCACCAAT | 79658 |
| rs191106972 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147815277 | GTGTCCTCTTCTGTT[G/T]TAGTGATAGTTAACC | 79658 |
| rs191117379 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147772154 | CTCTCTACTTCTGCT[C/G/T]TCTGCGCACTGGGAC | 79658 |
| rs191123369 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147786382 | GAGACTGGGAAGTCT[A/G]GGAGCCTGCTGCGGC | 79658 |
| rs191125516 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147867957 | TGTACAGTTCCTTAT[A/G]CTAAGGAGTGTAGCT | 79658 |
| rs191132411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147917934 | TTGTAAAAAAATCAT[A/G]AAACTGTTCACCTGC | 79658 |
| rs191138848 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147891243 | AATGTCTGTTAAGAG[A/C]TGAATGGATAAATAA | 79658 |
| rs191144405 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147759658 | GTATCCAAAATATTA[C/T]TTCAACGTGTAACCA | 79658 |
| rs191154567 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147854592 | TATATTTTTTTCTGT[A/C]ATGCAGTATTGGGGG | 79658 |
| rs191178544 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147954402 | GTTAACATTTAATAT[G/T]GTTTTGGCTTCATGA | 79658 |
| rs191184860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147991691 | TTTAGGGAATGTTTT[A/G]TATCAGTTTATAGAA | 79658 |
| rs191192506 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147793116 | CTGCACTCCAGCCTG[G/T]GCGACAGAGTGAGAC | 79658 |
| rs191194674 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147973729 | ATCATTCTGTTCTCT[A/G]TCTTCATGAGTTAAA | 79658 |
| rs191198376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148003843 | GAATACAGCACACTG[A/G]TAGGTCTTGACTCTT | 79658 |
| rs191209772 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148036123 | ACTTTTCCAGTTAAG[A/G]AAAACTAATGTATAA | 79658 |
| rs191213280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147823292 | AGCTTAATATATCAG[C/T]GGGATAAAAGCAGAA | 79658 |
| rs191213836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148017972 | AACATCCATTGTGTT[A/G]TGTCTGAGGAATCTG | 79658 |
| rs191227585 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148058807 | GGTTTGGCCCCACTG[C/T]TGCACGTGAAAGCTA | 79658 |
| rs191232467 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147760404 | GTTTCTACTTGGCAA[A/C/T]GTCAGGGTTTGAATC | 79658 |
| rs191239284 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147866535 | ATCATTTTCTATAAA[C/G]ACCAATTAATAGATA | 79658 |
| rs191256162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147830701 | ATTTTTGTATTTTTA[A/G]TAGAGACGGGGTTTC | 79658 |
| rs191277524 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147738838 | AAAATTGTCAAACCC[G/T]GGAAAGGCTTCCAAA | 79658 |
| rs191295598 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147935024 | ACCTGGCACATATCT[A/G]ATGAATAAATATATG | 79658 |
| rs191296038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147921179 | TTTGCTGAAGTTGTA[C/T]CAGTCACATTTAGCA | 79658 |
| rs191297002 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147897011 | TTTTTGCATATGTGC[A/G]TAATGACCCTTTTAT | 79658 |
| rs191308172 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147951931 | TTCCTCCTACCATTT[A/G]AAATCTCTCTCACAC | 79658 |
| rs191316932 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147970885 | CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 79658 |
| rs191330023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147968831 | TCATATGCCAGACAT[A/G]TAGTAGGTGCCGGAT | 79658 |
| rs191333482 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147986254 | AGCTACTCCATGCCT[C/G]TCACTGCCATTTCCA | 79658 |
| rs191335757 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148001008 | TCCTTGCCCATGCCT[A/G]TGTCCTGAATGGTAT | 79658 |
| rs191351512 | snp | C/T | 0.0854556 | 0.188216 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148001539 | TATTGATTCTTCCTA[C/T]CCATGAGTATGGAAT | 79658 |
| rs191354807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147836666 | AATCTAAGTACCAAG[C/T]AAGCTAGTACTTAGC | 79658 |
| rs191360751 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148014386 | TAAAACTGCACCTGG[A/T]GTGTTTTTAAAGGTT | 79658 |
| rs191362848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148033650 | GTTTAGTTTACAAAT[A/G]TTTCAGCTTAACTCC | 79658 |
| rs191367039 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148052195 | TCACTGGCAAACCCT[A/G]TCTTCACTTCCTCCT | 79658 |
| rs191380518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147872480 | GTGTTTATATAAACA[C/T]GTGTGCTCTGTGTAT | 79658 |
| rs191383830 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148071675 | GAGTTTGACTTTAAG[C/G]AGGGGAGTGATGTGA | 79658 |
| rs191389473 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147910212 | TGTTGTTGTTGAGAT[A/G]GGATCTTGCTATGTT | 79658 |
| rs191397807 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147844830 | AACGAGTCTGTCTTC[C/T]GGTTTTCTGTACCTT | 79658 |
| rs191403394 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147871389 | CAAGTAGGACTATTC[A/G]TGTCCGTCTCTCTAT | 79658 |
| rs191408159 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147945414 | GAAAGGATGTTTGTA[A/C]GAAACACATAATTAC | 79658 |
| rs191411139 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147938014 | TACATAAAGTACCAC[A/G]GACTACTATGCAGCC | 79658 |
| rs191415350 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147972962 | GTTTCTTCATGTTGG[C/T]CAGGCTGGTTTCGAA | 79658 |
| rs191427316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147777408 | GGACTACAGGCACCC[A/G]CCACCATGCCTGGCT | 79658 |
| rs191436105 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147736911 | TTGTCATAGGAGACG[C/T]GAAGAAGGATGGTTT | 79658 |
| rs191448790 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147813159 | TTTTTTTTTAAATAA[A/C]AGAATTGTATGTGTT | 79658 |
| rs191452465 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147754198 | TTATTTAGGTTAAGC[A/T]AAGAAGCAGATGCAA | 79658 |
| rs191453481 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147947792 | TCGAATCAACTTATA[C/T]GACGTATTTTGTATT | 79658 |
| rs191467350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147966511 | AAGGAGTAGGCAGGA[A/G]CATCTGCATGGAGGG | 79658 |
| rs191476860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148003463 | GAGTTTAATTCCTGG[A/G]TATCCTTAACTTTCT | 79658 |
| rs191478112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147848487 | TTTAGTTTCTTATAT[A/G]TAAAATGAAGGACTT | 79658 |
| rs191484959 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147983607 | CCGTTAAGACTTCCA[A/G]CTGTATTTTGAAATT | 79658 |
| rs191491975 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148011423 | GGGCTGACTCACAGG[C/T]TGGGCTCCCCTGGGA | 79658 |
| rs191493268 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148035904 | TACTACTCTATGGAC[A/G]GTAAAGAAGAATTTC | 79658 |
| rs191495947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148000321 | TTTCTTAATCCAGTC[C/T]ATCATTGATGGACAT | 79658 |
| rs191502065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148029801 | GAAGTTTAATCTAAG[A/G]CCAGGCTTGAATGTG | 79658 |
| rs191505422 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148059035 | GTGCATTTTCAGGAA[C/T]GTGTTTCCAAGTTAG | 79658 |
| rs191525667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147915322 | TTGTTTCTTATCCTG[A/G]TACCTCGAAAGAATT | 79658 |
| rs191562631 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147985880 | TAAGGGAAATGACAG[C/T]GGGAGGTCCTCTGCC | 79658 |
| rs191566870 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147950223 | CTATGTTATTTTTAG[C/T]GATGGAAAATGCAGT | 79658 |
| rs191596808 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148013712 | GAAAAGTTACTCTAG[C/G]CTACCCAAATGACTA | 79658 |
| rs191598207 | snp | A/G/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147790501 | CAAATATTCTAAGAT[A/G/T]TAACAAAACATTTGA | 79658 |
| rs191621399 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148013888 | GGTTCTCACTAGCCC[A/G]GGAGAGGAAGTCCTC | 79658 |
| rs191627211 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147863419 | CATGTTGTAGTATGT[A/C]TCAGAATTTCCTTCC | 79658 |
| rs191632207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148053446 | GAATCTGGTTGCTGC[A/G]CATTTATCATCTAAC | 79658 |
| rs191632563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147846736 | AAGTAGCTACAGTCC[C/T]AGTTCTTTACATAAT | 79658 |
| rs191634645 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147890464 | GAACCATTGTAACTC[A/T]ATAATATATAGACAA | 79658 |
| rs191641641 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B | ARHGAP10 | GRCh38.p7 | 4:148072938 | TATTCGGGGTGGGGC[A/G]TGTTCCTGGGGGCAG | 79658 |
| rs191644860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147828711 | TATGTTTGCATAGCC[C/T]CTTCCTTTCCCCCCT | 79658 |
| rs191651180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147810280 | GCATTCTTTTATTAC[C/T]AGTGAAGTTGGAAAC | 79658 |
| rs191653336 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147826894 | CCCTCCCCAAGCCCC[A/G]CCCTCAATAACAGTT | 79658 |
| rs191653988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148051741 | GTGCCTCAAGCTGTC[A/G]TTGTGCCACTGAGAT | 79658 |
| rs191659035 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147884026 | ACCACTGTGCCATAA[G/T]TCTCTGCAGATTACC | 79658 |
| rs191663287 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147904306 | TTACATATGTATACA[C/T]GTGCCATGCTGGTGT | 79658 |
| rs191672777 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARHGAP10 | GRCh38.p7 | 4:147731516 | AACGCTCTTGCCATT[G/T]TAAGGCTTCGATCTC | 79658 |
| rs191673028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147927921 | GTTACTAATGAAATC[A/G]GAAACTCCCTGTTAC | 79658 |
| rs191678041 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147864583 | GAGTCACAAGCTTTT[G/T]CTGCAAAGAAACTGA | 79658 |
| rs191718532 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147748153 | ACAGTTATGCTAAGA[C/T]AATAACCATGAACTG | 79658 |
| rs191722895 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147765206 | ATTGTGAGTCATTTA[A/G]GATCTATTTAGCAAA | 79658 |
| rs191727737 | snp | A/G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148017679 | ATATATATATATATA[A/G/T]ATATGTGTGTGTATG | 79658 |
| rs191740133 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147775676 | AATTCTGGCTCTGCC[A/G]CTCAGCCTATTAGTA | 79658 |
| rs191750140 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148058194 | GCTGTTCTAGACTTA[C/T]GCTGTATGTTTCCCA | 79658 |
| rs191767920 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147809549 | CTAAAGCTCAGAAGC[A/G]TTGTCACCTGCCCAG | 79658 |
| rs191772356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147738921 | GGCTCAGTGGCTCAC[A/G]TCTGTAATCCTAGCA | 79658 |
| rs191814373 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147925439 | TCTCTTTTTGATTTA[C/T]TGTAGTAAAATTTTG | 79658 |
| rs191820325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147943021 | GGAAAGGCAGGGAGA[A/G]ATATCAGATGAGTTG | 79658 |
| rs191825920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147900847 | CAACAACAACAACAC[A/G]CCTTGAGACAGGTTC | 79658 |
| rs191828281 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147908417 | CTGTTGGCAATGTCA[A/G/T]TGTAACCTTCAAGAC | 79658 |
| rs191830645 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147880155 | CTGCAGCTTATTACA[A/G]TAATTAATGGCCTAG | 79658 |
| rs191832360 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147861160 | GTGGCGAGGAGTTCG[C/T]GAGTGAGTTCAGGGT | 79658 |
| rs191836940 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147752254 | GATCTGATTTGGGGT[A/G]TTATCTTGTGTAAAG | 79658 |
| rs191846408 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147745232 | AACTGGGAGCCTGCT[C/T]GCAGAGGGCTGAGAA | 79658 |
| rs191851549 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147995777 | GCTGGAATGCAGTGG[C/T]GCGATCTCTGCTCAC | 79658 |
| rs191852537 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147761792 | TGTGCTGATTGGCAC[G/T]AAGTGACTTTGAAGG | 79658 |
| rs191854093 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147961289 | TAACTTCTGTTTCAC[C/T]GATATAGGTTTATTC | 79658 |
| rs191857140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147978996 | GCAGATATTTTCTCC[C/T]GTTTTGTAGATTGTC | 79658 |
| rs191860280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148007012 | TATTTTTGCATAATA[A/G]GATGTAGAAAAATTA | 79658 |
| rs191875846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148024010 | GCTAATCGTTGCCAC[A/G]TGGCCCTGTTGTTTC | 79658 |
| rs191903682 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148001389 | TTAGGATTGTCTTGG[C/G]AATGCGGGCCCTTTT | 79658 |
| rs191911010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147848739 | ATTTACTTTTACTTG[C/T]CATCTATTCTACTGG | 79658 |
| rs191937845 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148032823 | CCAGGAGTCCAAATC[A/T]GAAGAACTTGGACTC | 79658 |
| rs191942306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147886564 | CATAGTCACTCATCA[C/T]AGTCCCTTTTTAATA | 79658 |
| rs191947503 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148071415 | GAGGTCAGGAGTTTA[A/T]GAGCAGGCTGGCCAA | 79658 |
| rs191952139 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147959637 | GTTTTCTGTCCTTGC[A/G]ATAGGTTGCTGAGAA | 79658 |
| rs191960690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147923820 | AAGATTACAATGTAT[A/G]ATTTCAGTATTAATC | 79658 |
| rs191961684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147819861 | ACCGTGCACAGCCTA[C/T]TGTATCTTATTTACA | 79658 |
| rs191965159 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147940737 | TCTGCATCTTAAAAC[A/G]TTACAGCAAAGAGTC | 79658 |
| rs191972113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147764595 | GTGGAGTGCAGTGGC[A/G]TGATCTCAACTCCCT | 79658 |
| rs191976911 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147904550 | ATCCATGTCCCTACA[A/G]GGACATGAGCTCATC | 79658 |
| rs191979354 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147921741 | GGCAGCTCCTGTTCA[C/T]TCATCCCACCGTTTT | 79658 |
| rs191981769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147873336 | GAACATAAATAATAG[C/T]ATTATTGGCTTAAAT | 79658 |
| rs191982032 | snp | A/G | 0.209997 | 0.246779 | intron-variant, downstream-variant-500B | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147782964 | TAAATTATATATAAT[A/G]TATTAAATTATATAT | 79658 |
| rs191984658 | snp | G/T | 0.0209421 | 0.100162 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147800737 | TCTGCTATTTCCAGG[G/T]TTTATAGCGCTTAGT | 79658 |
| rs191987475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147975515 | CTGGAAAGCCCAAGG[C/T]TGATGAGCTGCATCT | 79658 |
| rs191990521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147802084 | TGATGACTGACAGGT[C/T]GGAGGAGTGGGGCGT | 79658 |
| rs191997570 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | ARHGAP10 | GRCh38.p7 | 4:147730998 | GCGATTCTCCTGCCT[C/T]AGCTGGGACTACAGG | 79658 |
| rs192003751 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147957141 | TTGGATGACAGGACC[A/G]TCAGAAAGAAATACT | 79658 |
| rs192004204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147837329 | TCAAGATTGTTTATA[C/T]GGTTCTGAAATTCTA | 79658 |
| rs192006673 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148028885 | ATAAAGTGGACATTA[G/T]TCGCCACAGATTAGG | 79658 |
| rs192006913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147992501 | CAACCTCCGCCTCCC[A/G]GGTTCAAGCCATTCT | 79658 |
| rs192011382 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148009419 | TTATAGCCATGAGGC[A/G]CCATGCCTGGCCGAG | 79658 |
| rs192046183 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147789082 | TGAGTGTGACCTCCC[C/G]TCTTAGCGTCTCCCA | 79658 |
| rs192062069 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147853377 | AAGTTCTTCTCTAGA[C/T]GAGTCCAACAGTAAA | 79658 |
| rs192077453 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147756658 | GGTATCCACACTGTA[C/T]GGTTGTATGTATAGG | 79658 |
| rs192078730 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147998778 | ATTCGTGATACCATA[C/T]TTCAATGAAACAGAA | 79658 |
| rs192084796 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147939076 | TGGAGATTTTCTTAC[A/C]CTTAATGCTACTCAG | 79658 |
| rs192104667 | snp | C/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148026611 | GCTTAAGCTTCTTTA[C/T]TGATGATTAATATGA | 79658 |
| rs192113580 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148064719 | CTATGCTTGCTTCTT[C/G]ATTACTCTCTGACCC | 79658 |
| rs192141954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147768380 | AGTGGTTTTTTGAGT[A/G]TCTGGAAACATTGTA | 79658 |
| rs192149408 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148007232 | ACACGCTTTTCTTTC[G/T]GAAAGAGATAATCAG | 79658 |
| rs192159270 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147996210 | GGAGAGAATAGCTAG[G/T]ATATGGCCTATGGAA | 79658 |
| rs192160506 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148024176 | AATAAGATGATTCTG[G/T]TATCCAAACCTGCGT | 79658 |
| rs192168008 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147936225 | CTTTTTTCCTGTATC[G/T]GGCTCAAAAGGTCTC | 79658 |
| rs192168091 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147842329 | GAAGGAAAAATATAA[C/T]GACCTAAGATTGCTC | 79658 |
| rs192171993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147970043 | TAACAGTTCTGAGAA[C/T]CTAAATTTCCCCATT | 79658 |
| rs192173395 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148042680 | ACACCACCTTGTTTG[A/T]CTTTGCCTGTCTTCT | 79658 |
| rs192175092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147735126 | ATTCAATTAGGTAGC[A/G]ATCTGCAAATATTTA | 79658 |
| rs192179153 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147950726 | TTTTAACTTCTCATG[G/T]TTTAGAGAGCTGAAT | 79658 |
| rs192187977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147916043 | GATCCCAGGGGTCGA[A/G]GCTACAGTGAGCTTG | 79658 |
| rs192190448 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148063760 | TCCTGTCAGTGGCTT[C/G]CCCCACACCAGTGAG | 79658 |
| rs192200256 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147879041 | TCCCAAAGTGCTGGG[A/C]TTACAGGCGTGAGCC | 79658 |
| rs192207916 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147803953 | CCTTGGATAAATATT[C/T]GATAGTGGGAATGCT | 79658 |
| rs192234658 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147980427 | TCTGATATGCTGCTG[A/G]ATTTGGTTTACTAGT | 79658 |
| rs192249152 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147907314 | ATTTTGATGGACTAG[G/T]GGCTTTTGAGAGTTG | 79658 |
| rs192262318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147867182 | TTGTTCCCAGATAGG[C/T]TTATCATTTGAGTAG | 79658 |
| rs192266104 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148007448 | CAGCTTGACAGGATT[G/T]CTCAGTAGCGAGAAG | 79658 |
| rs192276699 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148043125 | ATGGCGAAATGCAAA[A/T]TTGATGGCTGCAGAC | 79658 |
| rs192310785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147781508 | CTTGTCAAGACCCTC[A/G]ACTATGTTCATACTA | 79658 |
| rs192315946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147749331 | ATAACACCTTAGCTT[A/G]TTGTAGGCCAAGAAA | 79658 |
| rs192320904 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147766125 | GTCTTTACTGGAAAA[A/T]AAATAAATAAATAAA | 79658 |
| rs192323606 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148020536 | TTATAAGTGAGAACA[C/T]GCGTTTTTTGTTTTT | 79658 |
| rs192328231 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148039224 | TCTCTGAGAGTGTTA[C/T]CAGTATAGTTCTTCG | 79658 |
| rs192330405 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147956943 | GAGGTAGGAGCTTAT[A/G]TCTTAAGAGGTAATA | 79658 |
| rs192330980 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148060272 | TATTTAAAAAATGTT[G/T]CGATTCTTCTTATTA | 79658 |
| rs192334160 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147808557 | GCTGCTGTGTGGGAG[G/T]TGGGTTGGAGGAAAG | 79658 |
| rs192337881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147747637 | TTTCTAGAGCTAGAG[C/T]TGGTGTCCTGTTTTT | 79658 |
| rs192364711 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147932438 | GGATAAAGAAAATGC[C/T]GTACATGTAATATAC | 79658 |
| rs192367900 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147992270 | AGAAGCCAGGTGTTG[A/C]CACGTTTGTCCTGCT | 79658 |
| rs192375138 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148018461 | AATCACAGGTCAGAA[G/T]TTTAAAGTAAACAGT | 79658 |
| rs192426634 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147981950 | CTTTGAGCCCAGGGG[C/T]GTGATCATATGTGAG | 79658 |
| rs192434463 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147956275 | TTGAAAAACTTAGAG[C/T]ATTCCCTTTGGGACC | 79658 |
| rs192461289 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147779062 | CCCAGGGTTTGTGTG[C/T]ATCAGTCATCTGCTG | 79658 |
| rs192469736 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148008547 | CTTACAGTGCACAGG[A/G]CAATCCCTCCACAAC | 79658 |
| rs192482375 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147833493 | ATTACCCAGTCTCAA[A/G]CAGTAACTTCATAGC | 79658 |
| rs192483137 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148046146 | AGAGGGAAATAACTG[C/G]TCTTGTGAGCTCTCT | 79658 |
| rs192487350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147860487 | AACCAGGAGAAAATT[A/G]TGGCATATACCATGC | 79658 |
| rs192488563 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147816572 | CCAGAGACAATGTTG[A/G]CCCATGAGCTGCTTC | 79658 |
| rs192502033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147915716 | TTTGAATATTTTTCC[C/T]CCCAAAGGTCTTCCA | 79658 |
| rs192505175 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147797030 | TGTCTCCTTGGTTTG[A/G]AAGGACAGTGATGGA | 79658 |
| rs192509260 | snp | A/T | 0.0640965 | 0.167152 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147851271 | TTTTTTTTTTTTTTT[A/T]AAATACAGGATTTCA | 79658 |
| rs192514534 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147878311 | AACGTTGGCCAGGAT[A/G]GTCTCCATCTCCTGA | 79658 |
| rs192514885 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147739547 | TGGAAATCCTAACAG[C/T]TTGTATTTGCTATGG | 79658 |
| rs192515659 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147898332 | TAAAGAAGTCATTTC[A/G]TTGTCTTCAGGCTTC | 79658 |
| rs192516609 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147756764 | CCCTGGATAAGGGGG[G/T]ACCACTATATTGTTA | 79658 |
| rs192522601 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147744678 | CTCAGGTTCTGGTGT[C/G]GGCTGGTGAGTGCAG | 79658 |
| rs192535881 | snp | C/T | 1.66576e-05 | 0.00288592 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148063304 | GCCACCTGAAAGGTA[C/T]GTGGTTTGGAGTGGA | 79658 |
| rs192540052 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148033721 | TTAATATTTTGTAAT[G/T]GAAGGACTGAGAAAC | 79658 |
| rs192549449 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147860831 | GAAATTGTGTATTTG[C/T]TAAAAACTAGTGATT | 79658 |
| rs192551081 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147809991 | AGACTACTGCTATTA[A/T]CAACTGTCATTCTAT | 79658 |
| rs192569292 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147825279 | ACCTGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 79658 |
| rs192579172 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147898686 | ACCTGATTTCCATTT[C/G]TGTGTGTTTGGATCA | 79658 |
| rs192584106 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147775922 | CCACAACAACATCTC[C/T]GTTTTACACACTAGG | 79658 |
| rs192592694 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147789424 | CCTCCTGGGTAGCTC[A/G]TATTACAGGCATGTG | 79658 |
| rs192598811 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147873923 | GGAGAAATGGAAGGC[A/G]AGAGGGAACCTAGCC | 79658 |
| rs192601542 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147856311 | GGTGAGTACTGGTAT[A/G]TCAATATTATTTTAG | 79658 |
| rs192607670 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147838293 | TGTTAGCAGCCCATT[G/T]GGACAGTCTCTTTAA | 79658 |
| rs192615884 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147912037 | TGTGTGTGTGTGTGT[A/G]TGTATAGTTTTCTTT | 79658 |
| rs192629152 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147936301 | CTGGCAGGGCTGTGC[A/G]GCCTCCTTTTCCTCT | 79658 |
| rs192629793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147758012 | TATTGGTTTTATAAA[C/T]GTTACATTAGATAAA | 79658 |
| rs192634312 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147893271 | CCTTGTTGGTCAGGC[C/T]GGTCTTAAACTCCTG | 79658 |
| rs192656559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147819201 | CCATATGAAACACCA[C/T]CTTTAAAATAACCTG | 79658 |
| rs192661663 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147931608 | AAGCAAAAACCAAGG[C/T]TGACCAAGTATCTTT | 79658 |
| rs192664171 | snp | C/G | | | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147782181 | CTGAATTTAATTGTG[C/G]TGGGTGTGTGGGGTT | 79658 |
| rs192668574 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147966124 | TTTACAAAGGTGCTA[C/T]GCAGTCTAGTATTCC | 79658 |
| rs192668644 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147947589 | TGTAATTTTAGTAGA[A/G]GTGGGGTTTCGCCAT | 79658 |
| rs192683419 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148024777 | TCAGCAGAGTTGTTA[A/G]TAAGGAGTAAAACTG | 79658 |
| rs192692194 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148063959 | AGCCCCTTCTAGAGC[A/G]GTGGCCACCCGGAGT | 79658 |
| rs192709320 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147736252 | GCCTGGACAAGAATT[C/T]AGGTCTTCCGACTTG | 79658 |
| rs192714821 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147940145 | GGTTGACTATCTTCC[A/T]GTGCTTGCTTCTCAC | 79658 |
| rs192724041 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147975372 | TCACGGAGGAGCCTA[G/T]ACAGAGCAGTAGGGA | 79658 |
| rs192732545 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147795126 | CTCACTGTGTCACCT[A/G]CGCTGGAGTGTAGTT | 79658 |
| rs192736512 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148003940 | ATGTGAAGAAAGCTG[C/T]AAAATTATGCTAAGA | 79658 |
| rs192744246 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147832577 | GCTTGAACCTGGAAG[A/G]CGGAGGTTACAATGA | 79658 |
| rs192747851 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148037051 | GTTCTTTGGTCATGA[A/T]CTTTTTCAGTTTCCC | 79658 |
| rs192763421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148067526 | CCACAGGAGTACTGC[C/T]GGGAATGCTCCCTTT | 79658 |
| rs192763526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147869351 | ATAACACACCTGTTG[A/G]GGGGGCGTCTGTTTA | 79658 |
| rs192790488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147936415 | CTCACTGCAAGCTCC[A/G]CTTCCCGGGTTCACG | 79658 |
| rs192790815 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147761133 | GCAATCCTCCTGCCT[A/C]AGCCTCCCGAGTAGT | 79658 |
| rs192795641 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147971161 | TTTCTTCCTTTGTTA[A/T]CGAGAAAATTTTATT | 79658 |
| rs192800726 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148002460 | ATTTCCTCTTTTTCT[A/G]TTGATTGGCATAGTT | 79658 |
| rs192801085 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147794116 | GGGAGGGACAGGCTC[A/G]AACACAAATAATTAT | 79658 |
| rs192820451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148014922 | TAGAAAAGTACTTTT[C/T]TCTTCTTTTAGTTTT | 79658 |
| rs192824857 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147811138 | GTTCAACAGCTTCTG[A/T]TAATAAGGGACTTCT | 79658 |
| rs192829174 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147884481 | GGGTTCCCTTATTAA[A/G]GAGGCATAGGGGCCT | 79658 |
| rs192839414 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911605 | CTGACTTCGTGATCC[A/G]CCCACCTTGGCCTCC | 79658 |
| rs192839442 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147847036 | AGAGTGAGATAAAGC[C/T]GTTAAATACGTTCAT | 79658 |
| rs192849330 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147946910 | GCAACAGAACAGAAA[C/T]TGACATAGACTTGGG | 79658 |
| rs192850209 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147982830 | ATGCCAATAAGGTAT[A/T]CATTTGGTTGTTTTA | 79658 |
| rs192865845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147801180 | CATTTATTTTTCTAC[A/G]TTCAGTAAAACATAT | 79658 |
| rs192869846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147776303 | CGGCTCACTGCAACC[C/T]CTGCCTCCTGGGTTC | 79658 |
| rs192877500 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148038921 | ACAGTTTTTTTTGTT[C/T]CTAAAGTGGTGCCTT | 79658 |
| rs192883085 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147739919 | TTTTGTATTTTTTGT[A/G]GAGATGGGGTTTCAC | 79658 |
| rs192905363 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147926380 | GATAGGAAGAGAGAC[C/T]TCGCAGACAAACAGA | 79658 |
| rs192912307 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147887407 | ATTAGTTTTGGCTCC[C/T]GGCAGCAAGTGAAAT | 79658 |
| rs192916046 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147753085 | ATAGTATCAGTGAAG[A/G]CACTGTAGTCAGTTT | 79658 |
| rs192919478 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147986088 | GTGGCTGAGGTATGC[A/G]GAAAGCCTCTCATCT | 79658 |
| rs192926798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147961656 | AGGTGTTCTGAAATC[C/T]CACTCTTCTCCCCTT | 79658 |
| rs192957167 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147815960 | CGTTGTTGTAAGCCA[C/G]TGCATTTGTGGCAAT | 79658 |
| rs192958124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147778706 | ATGATTCCTGGATGT[C/T]GCTCCTTTTTGCTCC | 79658 |
| rs192967288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147887052 | GCGAGTCACCCTGCC[C/T]GGCCCATGCTATGTT | 79658 |
| rs192972069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147850553 | ACTGCAAAGGTCTGC[A/G]GCTTCACTCCTAAGT | 79658 |
| rs192990778 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147953107 | TGCTAGTATTGTATT[C/T]CTGTGATAAACCCAA | 79658 |
| rs192993567 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147916691 | GATACGGGGTCCATC[A/G]CTGATGTTATAAAAG | 79658 |
| rs193006417 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148029617 | GTAACTGGACTAAGC[A/C]GACCTTTGCATTAAG | 79658 |
| rs193009137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148042278 | ACTGTCATAACTGAA[C/T]ATCTTTTGAAGCTGT | 79658 |
| rs193010096 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147987825 | AAGAGGAGTGGGAGA[G/T]AAGTGGAGACTTGCT | 79658 |
| rs193013426 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148066871 | ATAGACGTATGGGGG[A/C]GAGGCTGCTGACCAC | 79658 |
| rs193027343 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147829235 | TTTTTTGTATTTTTA[C/G]TAGAGACAGGGTTTC | 79658 |
| rs193040000 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147930797 | TCACATTTATTTGCC[A/C]GCTGTAGCTACTCTA | 79658 |
| rs193044118 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147892049 | AAAGAAAATGCTTCC[C/T]GTTTTGCTCTCATTA | 79658 |
| rs193044151 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147865469 | GAAACACATGATTTT[C/T]GTTTGTGATTATATA | 79658 |
| rs193055672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147785914 | TTTCATAATTTGTCA[C/T]CAAATACATTTTTCA | 79658 |
| rs193059931 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147965488 | AAGTTGGCTTAATTC[A/C]ATAATGGGTAGTTAT | 79658 |
| rs193064003 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147999680 | TAGAGCTCTAACACT[C/T]ACCACATGGCCCAAG | 79658 |
| rs193073101 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147753779 | TTTTCATGATGCTCA[C/G]GTATTCATGAATGTT | 79658 |
| rs193082385 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148018855 | TACCATTTTGAAACC[A/G]TGGAGACTTGTGCTA | 79658 |
| rs193085643 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148059159 | TGCTGAAGATAGAGA[A/C]GAATCCTGTTTTAGG | 79658 |
| rs193088373 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147824854 | AGCCAAACCATATCA[A/G]CCAGGAGCTGTTCTA | 79658 |
| rs193118060 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147733056 | TCCGCACATTCCTCC[A/C]CTGCCGTGCTGAGGA | 79658 |
| rs193119310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147864179 | TCCTGCTCTTCTCCC[A/G]GTTCCTTTCTAGTTA | 79658 |
| rs193123468 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147766836 | TATATATATATATAT[A/T]TATTTATTTATTTAT | 79658 |
| rs193124864 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147903954 | TCTTGTGTAGACATA[A/G]TTTTCAGTTCCTTTA | 79658 |
| rs193135868 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147826033 | GGAGCCAGGTGGGGC[A/G]GGGCTACAGCATATC | 79658 |
| rs193145598 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148000223 | GAGAAGGATGGTTTC[C/T]AGCTTCATCCATGTC | 79658 |
| rs193160372 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147908830 | GTCCCTTTTAAGGAC[C/T]CTGCCCCCTTTATCT | 79658 |
| rs193164877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147943664 | TAACAAACCCATAAA[A/G]TGTCCTTCCTTGGTC | 79658 |
| rs193165327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147979475 | AGTATTGTTTGAAGC[C/T]GGCTTTGTTCCTTTT | 79658 |
| rs193205963 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148048011 | TAGTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 79658 |
| rs193237165 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147806060 | AATCCATACTTTAAG[A/C/G]CTTTTGTTTATATTT | 79658 |
| rs193237835 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147736653 | GTCTGCATCCTTTTC[A/G]GATGACTCAGGGGAA | 79658 |
| rs193240601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147771769 | ATTCTCATCTTCCTC[A/G]CCTCCACTCTTGCAA | 79658 |
| rs193244361 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147842242 | TGCCTGGCCGTGAAA[A/C]CCTTATATTCTTTTT | 79658 |
| rs193249715 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147870347 | ATTACAGGCGTGAGC[C/T]ACCGCGCCCGGCCGC | 79658 |
| rs193267275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147783318 | TATATAACACACATT[A/G]AATTATGTATTGTAT | 79658 |
| rs193272581 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147820359 | GGTGTGATCCTGGCT[C/T]ACTGCAACCTTCGCC | 79658 |
| rs193275100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147846482 | TTTCTTTTATTTGCA[C/T]TTTCAGCATTTTGTG | 79658 |
| rs193276134 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147750613 | TATCTTTTTTTTTTT[G/T]TGGGGGGGGTTGTAA | 79658 |
| rs193288534 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147919402 | GGCATGTGTGGGAGT[C/G]ACATCAACTCGTCTT | 79658 |
| rs193299067 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147983183 | CATGGTGCCTGGCTG[C/T]TTTGTTTTTTTTTTT | 79658 |
| rs193300221 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148010260 | CCCTTTTAGCTGGAT[C/T]AGGAGACTGAGCTAT | 79658 |
| rs199505952 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148061625 | AATGTTTTTTTTTTT[A/T]AAATGACCCCCTTTT | 79658 |
| rs199513423 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147744217 | TTCTAGGCTGAGACC[A/T]AAAGGAGGGATCAGA | 79658 |
| rs199526928 | snp | A/C | 3.35864e-05 | 0.00409781 | utr-variant-3-prime, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148072098 | TCCTGGCCTCAGAGC[A/C]CCTGCTGACCCTGGC | 79658 |
| rs199543274 | in-del | -/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147874036 | GTGTTTAAAAAAAAA[-/C]AACAAACCTCTGCAG | 79658 |
| rs199553734 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147899893 | TTTTTTTTTTTTTTC[A/G]TTTTCAACATTCCTC | 79658 |
| rs199570711 | in-del | -/TAATT | 0.0107246 | 0.0724382 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147918113 | GCTGAATAAGAAAAA[-/TAATT]TAAACTCTCATTAAG | 79658 |
| rs199603704 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148059523 | AAGGACTCTCAAAAA[A/T]TTCATTATGTTCTAG | 79658 |
| rs199604591 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147969317 | ATGTGAGAAGTTTTG[-/T]TTTTGCCTTTTTTTT | 79658 |
| rs199607031 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147757487 | AGGTGTGAGCCACCG[C/T]GCCTGGCTGGGGCAG | 79658 |
| rs199635167 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147768690 | TGACAACTTTGTTTT[C/T]GAGTTTGTTTAAACA | 79658 |
| rs199637772 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147765349 | GTGTGGGGGGGGGGG[A/C]GTGAGTGTGTGTATT | 79658 |
| rs199653111 | in-del | -/TG | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147865590 | TCAGCAAAAAAACAC[-/TG]GATCTCATTCTCAGG | 79658 |
| rs199654685 | in-del | -/A | 0.0182019 | 0.0936463 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147941979 | TTTAACGCCTCTTCC[-/A]AAAAAAAGGGTTTTA | 79658 |
| rs199670329 | in-del | -/T | 0.0193772 | 0.0965046 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148016541 | AAAAAATGCAAATTG[-/T]TTTTTTTCTCTGTTC | 79658 |
| rs199673665 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147880909 | ATAAATTTTTACACT[A/T]AAAAAAAGAGTACAA | 79658 |
| rs199688188 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147922427 | GGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 79658 |
| rs199690124 | in-del | -/A | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147887683 | CTGACCGATATGGTT[-/A]AAACCCCATCTCTAC | 79658 |
| rs199691254 | in-del | -/GTT | 0.0463947 | 0.145069 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147792687 | TTATGATTTATCCAA[-/GTT]GTTGTGTTGGCTTTG | 79658 |
| rs199696238 | in-del | -/AAAT | 0.0236746 | 0.106192 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147766126 | TCTTTACTGGAAAAA[-/AAAT]AAATAAATAAATTAG | 79658 |
| rs199714695 | snp | A/T | 6.60949e-05 | 0.00574831 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147906762 | TTTCAAAGCCTTTAG[A/T]GTTGACTTGCATTCA | 79658 |
| rs199718309 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148018483 | GTAAACAGTTTTACT[A/C]TTTCCTCTTCTTGTA | 79658 |
| rs199743334 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148054313 | TAAGCAAACCAGGGA[G/T]TTAAGCAAACCAAGG | 79658 |
| rs199743384 | snp | A/G | 4.04883e-05 | 0.00449917 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147966887 | TTTCGGCTTGTCGCC[A/G]TGTACTACACAACGA | 79658 |
| rs199759286 | in-del | -/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147751888 | AAGCCTTTAGTTTTT[-/G]TTTTTTTTTTTTTTT | 79658 |
| rs199778485 | in-del | -/C/CCA/CCTGTAACC | 0.336272 | 0.235283 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147924745 | TCCTTATTAACTCTG[-/C/CCA/CCTGTAACC]CCTGTAACCTCTCTG | 79658 |
| rs199792222 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148062008 | AAGATTAGAGCAGGG[C/T]GGGGAGCTTGAGAGG | 79658 |
| rs199796619 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911644 | TGGGATTACAGGCGT[A/G]AGCCACCGCGCCTGG | 79658 |
| rs199800667 | in-del | -/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147877273 | TGCAATATTTTTTTT[-/G]TCAACCATAGAACAC | 79658 |
| rs199814256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148066780 | TTCTTCATCCTAAGC[A/G]GCAGGGATGGCCACA | 79658 |
| rs199815485 | snp | C/T | 0.000100247 | 0.0070791 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147879378 | TAGATTATAATCTGT[C/T]AGAGGTAGTGTTTGA | 79658 |
| rs199826145 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147853778 | TCTTATGGCTTCTTT[C/T]TTTCCTTTTTTGCTT | 79658 |
| rs199842614 | in-del | -/T | 0.00478085 | 0.0486577 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147832073 | CTCTCTTCTTCCCCC[-/T]GACTGCCCCGCCCGA | 79658 |
| rs199848122 | snp | A/G | 1.64746e-05 | 0.00287002 | synonymous-codon, intron-variant, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148063178 | ATCGTCTATGGTCCA[A/G]TGGCTTAACCCACAG | 79658 |
| rs199850686 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147811603 | TTTAAAAAAAAAAAA[A/C]AAAAAACAAAACACT | 79658 |
| rs199864383 | snp | A/G | 4.95201e-05 | 0.0049757 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147822945 | GAATCTGGAGGAACA[A/G]AGAGAAATTATGGTG | 79658 |
| rs199882780 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147753355 | ATTTTCTTTTCTTTT[C/T]TTTTTTTTTTTTGAG | 79658 |
| rs199898539 | in-del | -/AAGTA | 0.0256215 | 0.110247 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147880707 | TCTGCATTGCAAATT[-/AAGTA]AAGATAAATTCAGGG | 79658 |
| rs199902147 | in-del | -/A | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147851271 | TTTTTTTTTTTTTTT[-/A]AAATACAGGATTTCA | 79658 |
| rs199935792 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147785223 | AATCTAAAAATAAAA[A/G]CACAAGGCTGTAGTT | 79658 |
| rs199963512 | snp | A/G/T | 0.000197757 | 0.00994191 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147866754 | ACCTTCTATCATCAG[A/G/T]GCCATGAACTTGCCA | 79658 |
| rs199972892 | snp | G/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147939855 | GATTGTACAGAGTTG[G/T]GGGGGTGAGTTCAAA | 79658 |
| rs199973251 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148013691 | AGACTCCATCTCAAA[A/G]AAAAGGAAAAGTTAC | 79658 |
| rs199978457 | snp | A/G | 0.00199792 | 0.0315431 | synonymous-codon, intron-variant, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148063247 | TCTTTCACCCGGGTC[A/G]TCCCCTTTCCCCTTT | 79658 |
| rs199982785 | in-del | -/TTA | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147742381 | AGGTGCCTATTATTT[-/TTA]TTATTATTATTATTA | 79658 |
| rs199985726 | in-del | -/A | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148046269 | TTGTGCAACTCATTT[-/A]AAAAAAAAATTTAGC | 79658 |
| rs199997876 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147933827 | TTGGTATCTGCTGTG[A/G]GGCAGAGGCTGGAGA | 79658 |
| rs200063962 | snp | C/T | 5.32127e-05 | 0.00515786 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147875184 | GTGGCTGCGTGGCTG[C/T]TTAAAAATGCAAATT | 79658 |
| rs200067233 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147812454 | CACATTCATTTTCTA[A/C]CAGCCACATTTCCAG | 79658 |
| rs200069654 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147762528 | TATTTATTTTTATTT[A/T]TTTATTTATTTATTT | 79658 |
| rs200079677 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147919576 | AAAACAATTTTTTTT[C/T]CTTTTTTTTTTGTGG | 79658 |
| rs200082973 | in-del | -/C | 0.0103295 | 0.0711199 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147838639 | CTCGGCCTCAACTAG[-/C]CTCCCACCTCAGCCT | 79658 |
| rs200095874 | in-del | -/AC | 0.184521 | 0.241273 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147783908 | TATTATATTTATATA[-/AC]ACACATTAAATTGTG | 79658 |
| rs200097967 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147953642 | TGTTTGTTTTCTCTC[C/T]TTTATTTCCTAATCA | 79658 |
| rs200104606 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147920128 | CTTTTAAAAAACAAC[A/C]TAACCTCGCTGGGCA | 79658 |
| rs200106697 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148071637 | AAAACAAACAAACAA[A/C]CAAAAAAAAACACAA | 79658 |
| rs200108416 | in-del | -/C | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147798827 | TATATAGACTTTTTA[-/C]CCCCCCACGCTTGAA | 79658 |
| rs200118899 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147988598 | ATACACACACACCAA[A/C]AAGTGTACACTTTCA | 79658 |
| rs200128716 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147931328 | GAAAAAAAAAAAAAA[C/T]TTGGGGCCTGTAAAC | 79658 |
| rs200133329 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148001027 | CCTGAATGGTATTGC[C/T]TAGGTTTTCTTCTAA | 79658 |
| rs200137654 | in-del | -/A | 0.0154538 | 0.0865337 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147793138 | AGTGAGACTCTCTGG[-/A]AAAAAAAGAAAATGT | 79658 |
| rs200150632 | snp | A/C/G | 3.30225e-05 | 0.0040633 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147955391 | TAAGTATTATGTAAA[A/C/G]GTATATAGGAACAGT | 79658 |
| rs200153083 | in-del | -/T | 0.02016 | 0.0983543 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147897161 | TCTTTATGTTTAAAC[-/T]TTTTTTTATAAACAG | 79658 |
| rs200160327 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148003787 | CCTCCATCCCTTTAT[G/T]TTGAGCCTGTGTGTG | 79658 |
| rs200165288 | in-del | -/GTG | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147870000 | AAAAAGTCCCAGTTT[-/GTG]TGTGTGTGTGTGTGT | 79658 |
| rs200168461 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147784770 | TAAAATGTATATTAT[A/G]AATATAATATATTAT | 79658 |
| rs200174355 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147747072 | GGGTAAACAACCCTC[A/G]TGATACCCAGAAAGG | 79658 |
| rs200176860 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147761017 | TTTTTTTTTTTTTTT[-/T]GACACAGAGTCTTGC | 79658 |
| rs200184056 | snp | C/T | 9.93229e-05 | 0.00704639 | synonymous-codon, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148072066 | GATTCCACAGAACTA[C/T]GTCAAGCTGCTGTAG | 79658 |
| rs200209180 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147772266 | AGCAGTGGACTTCAG[C/T]TCCCTCTCCCTAGGT | 79658 |
| rs200211443 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147771501 | TAAAATGTATGATTA[A/T]TTTTGACTATAGTCA | 79658 |
| rs200226193 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147851270 | ATTTTTTTTTTTTTT[A/T]AAAATACAGGATTTC | 79658 |
| rs200227783 | in-del | -/AG | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147892185 | TTTTTATGTTGAGGA[-/AG]AGAGGAGGAAATCAC | 79658 |
| rs200235578 | in-del | -/GT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147791522 | TTGAATGGTTATTCC[-/GT]GTGTGTGTGTGCGCG | 79658 |
| rs200237726 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147764485 | ATAGTGACTTTGAGG[-/T]AAAAAAAAAAAACCT | 79658 |
| rs200262956 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147742919 | CTTTTTTTTTTTTTT[A/T]AAGTTTTGGGGACAA | 79658 |
| rs200269811 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147890297 | GCCATTACTACTTTG[A/T]TTATCAATGGTTAGA | 79658 |
| rs200271996 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147868255 | TTTGTTTTTTTTTTT[G/T]AGACAGGGTGTCACT | 79658 |
| rs200272898 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147893081 | TTTTTTTTTTTGAGA[C/T]GGAGTCTTGCCCTGT | 79658 |
| rs200273649 | in-del | -/TATA | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147855668 | AGAAAACTTAGGTTC[-/TATA]TTGTCAGATGGTTTT | 79658 |
| rs200278279 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148049855 | CGGGGGGCGGGGGGC[G/T]GGGGGTGGTGGTGGC | 79658 |
| rs200325163 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147870946 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT | 79658 |
| rs200329568 | snp | C/T | 0.00158123 | 0.0280734 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148023276 | AGATTTTTCGGACGC[C/T]GCCCGATACTACATT | 79658 |
| rs200333777 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147737737 | AATGTAGACCGGCTG[A/C]GAAAATAATTACAAT | 79658 |
| rs200341059 | in-del | -/A | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147793320 | CATATATATATATAT[-/A]TTTTTTTTTTTTTAC | 79658 |
| rs200341810 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147815539 | CACAGTGGTCCTTAA[A/G]AGAGAGAAGAGATGT | 79658 |
| rs200353266 | in-del | -/GCTAAGTGTTAA | 0.0352966 | 0.128072 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147833704 | AATGTATATAAAAGT[-/GCTAAGTGTTAA]GCTATTATTTCAAGA | 79658 |
| rs200364964 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147904804 | TCCCTGAGGAATCGC[C/T]ACACTGACTTCCACA | 79658 |
| rs200365132 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147785101 | AAAAAAAAAAAAAAA[A/G]AATAACATCTAAGCT | 79658 |
| rs200385925 | in-del | -/CTT | 0.00993419 | 0.0697739 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147743772 | ACAAGAGTGAAACTC[-/CTT]CTCAAAAAAATAAAT | 79658 |
| rs200387773 | in-del | -/TA | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147811590 | TGCAATGGCTTTTTT[-/TA]AAAAAAAAAAACAAA | 79658 |
| rs200388255 | snp | C/T | 1.65097e-05 | 0.00287308 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148064426 | TTCAGCATCCGCAGT[C/T]GGAAGGCTCGAGCCG | 79658 |
| rs200413212 | snp | C/T | 0.00797118 | 0.0626263 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147920341 | AGAATGGTGTGAACC[C/T]GGGAGGTGGAGCTTG | 79658 |
| rs200431111 | in-del | -/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147750613 | ATCTTTTTTTTTTTT[-/G]TGGGGGGGGTTGTAA | 79658 |
| rs200437362 | snp | A/G | 0.000747477 | 0.0193179 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147879355 | TAAGTATTTGATTCA[A/G]CATAGAATAGATTAT | 79658 |
| rs200443508 | in-del | -/AAAC | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147912531 | CAAAACAAAAACAAA[-/AAAC]AAACAAACAAACAAA | 79658 |
| rs200445508 | in-del | -/AT | 0.286303 | 0.24735 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147784534 | TATATAATATAAAAC[-/AT]ATATTTTATAGTATA | 79658 |
| rs200445702 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148038994 | TATATTTCTCTCCCC[A/C]CTTCCAATAAGACAA | 79658 |
| rs200468797 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147788496 | GAAGGTATGAAGGAA[A/G]ACTTGTGAAAGCACT | 79658 |
| rs200477049 | in-del | -/TGTA | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148036103 | GTGTGTGTGTGTGTG[-/TGTA]TACTTTTCCAGTTAA | 79658 |
| rs200484989 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147908311 | GCAGGAAGTATATTG[C/G]ATTTGCATCCATTAA | 79658 |
| rs200485045 | in-del | -/TACTTT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147749000 | ACATAAGATAACTTT[-/TACTTT]TGAAACTCACTTTAT | 79658 |
| rs200501384 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147881977 | AAAGAGTCGTTTTAA[A/T]AAAATGATTTAAAAA | 79658 |
| rs200524861 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148052395 | TTTGCACATTTGCTT[C/T]TTTTTTTTTTTTTTT | 79658 |
| rs200528538 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148060027 | GAGAGGGGAGAGAGA[A/C]GAGAGAGAGACGAGA | 79658 |
| rs200578124 | snp | A/G/T | 0.00172845 | 0.0293472 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148046963 | TCCTCCCCGTCTCCC[A/G/T]TGACTACAGCTGTCC | 79658 |
| rs200580640 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147943732 | GAACATGTATTCTGA[A/G]TGAACCCTCCAAATG | 79658 |
| rs200581454 | snp | A/G/T | 1.67279e-05 | 0.002892 | utr-variant-3-prime, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148072093 | GTAGCTCCTGGCCTC[A/G/T]GAGCCCCTGCTGACC | 79658 |
| rs200584137 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148017680 | TATATATATATATAT[A/G]TATGTGTGTGTATGT | 79658 |
| rs200604450 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147894141 | TTGCATAAATACTTT[G/T]GGTGTGGGAATTGCT | 79658 |
| rs200622324 | in-del | -/TATAT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148017675 | ATATATATATATATA[-/TATAT]ATATGTGTGTGTATG | 79658 |
| rs200625852 | in-del | -/T | 0.0916144 | 0.193427 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911643 | CTGGGATTACAGGCG[-/T]GAGCCACCGCGCCTG | 79658 |
| rs200627348 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148045766 | AAAAAAAAAAAAAAA[C/T]AAATCCATCTAAGAT | 79658 |
| rs200635880 | in-del | -/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147982368 | TTTCTTTCTTTCTTT[-/C]TTTTTTTTTTTTTCT | 79658 |
| rs200649105 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147987901 | GAGTCCCAGCTCTTG[G/T]TACTTCCTGCTGATT | 79658 |
| rs200661073 | in-del | -/TG | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147776113 | ATCATTTATGGCCTC[-/TG]CTCGTAATCATTAAC | 79658 |
| rs200667293 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147914846 | CAATAACCCAAAACA[-/T]TTTTTTTTTAAGTCT | 79658 |
| rs200677159 | in-del | -/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147865579 | TCATGTGGATTTCAG[-/C]AAAAAAACACTGGAT | 79658 |
| rs200681201 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147762524 | TATTTATTTATTTTT[A/T]TTTATTTATTTATTT | 79658 |
| rs200681323 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911996 | TTAAGAACATTCACG[C/T]GTGTGTGTGTGTGTG | 79658 |
| rs200687367 | snp | A/G | 0.000115336 | 0.00759305 | synonymous-codon, intron-variant, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148063166 | AGGCCAGACCCGATC[A/G]TCTATGGTCCAGTGG | 79658 |
| rs200755482 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148003846 | TACAGCACACTGATA[A/G]GTCTTGACTCTTTAT | 79658 |
| rs200756755 | in-del | -/TGTGTGTGGG | 0.0217236 | 0.101931 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147766547 | GGCTGTCTGTATAAC[-/TGTGTGTGGG]TGTGTGTGGGTGTGT | 79658 |
| rs200798111 | in-del | -/TCTA | 0.0551013 | 0.156571 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147893455 | TATATTATTATTCTC[-/TCTA]TATATAATACTATTC | 79658 |
| rs200803279 | snp | A/C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147769066 | TGAAAATTAAAAAAA[A/C/T]ATAAAAAAGGGCAGA | 79658 |
| rs200804383 | snp | A/G | 4.94907e-05 | 0.00497422 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147822705 | ACAAGAACCCAAGTC[A/G]TCATTATACTTTTCT | 79658 |
| rs200809778 | snp | C/G | 1.66663e-05 | 0.00288667 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147732418 | GTTCATCAAAGAGCT[C/G]ATTAAGGACGGGAAG | 79658 |
| rs200820606 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147735906 | TCGTGATGTCTATGT[A/G]GTTTCAGTTGCTTAT | 79658 |
| rs200822305 | in-del | -/TTTTTT | 0.304188 | 0.244057 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147830513 | CAAAACCACAATTCC[-/TTTTTT]TTTTTTTTTTTTTTT | 79658 |
| rs200827579 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147890293 | GCTAGCCATTACTAC[-/T]TTGATTATCAATGGT | 79658 |
| rs200828880 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147958384 | TTCAGTGTATTTCTT[A/G]CTGTAGTCAAGTTAG | 79658 |
| rs200833731 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147922460 | TTTGGGAGGCCGAGG[A/C]GGGCGGATCACGAGG | 79658 |
| rs200844477 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147869593 | TATTGAAAAAAAAAA[A/G]GCCTTTTTTGTATTC | 79658 |
| rs200847076 | snp | A/C/T | 3.29561e-05 | 0.00405921 | synonymous-codon, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148023322 | CCTGTCAGCATCACC[A/C/T]CCAAATGCGCCACCA | 79658 |
| rs200856201 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147832341 | TATTTGACCACTTAA[-/T]TTTTTTTTTTTTTTT | 79658 |
| rs200858620 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148060344 | ACGAAGCTCATGTTT[A/T]GTTTTTTTTTTTTTT | 79658 |
| rs200860294 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147741782 | TACACACACACACAC[A/G]CACACACACGCACAC | 79658 |
| rs200869815 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148045479 | GGGTGCAGTGGCTCA[A/C]GCCTGTAATCCCAGC | 79658 |
| rs200880348 | snp | A/G | 0.000798403 | 0.0199641 | synonymous-codon, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148046983 | TACAGCTGTCCCTGG[A/G]CCTCCTGGACCAGAC | 79658 |
| rs200880946 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147780226 | CCTTTTCTGTGGCTG[G/T]GGGTGGATCTGGGAG | 79658 |
| rs200889352 | snp | C/T | 4.94271e-05 | 0.00497102 | synonymous-codon, intron-variant, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148063241 | GACACCTCTTTCACC[C/T]GGGTCGTCCCCTTTC | 79658 |
| rs200903781 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147832666 | AAAAAAAAAAAAAAG[C/T]AAATTGGAGCTCATT | 79658 |
| rs200912344 | in-del | -/GAGATTG | 0.00953873 | 0.0683987 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147867656 | AGATCGCGAGGTCAA[-/GAGATTG]AGACCATGCTGGCCA | 79658 |
| rs200919109 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147970577 | TCCTCCCTAAGAATG[G/T]GAAAAATGTTGACTC | 79658 |
| rs200933961 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147954524 | TTTGATTTTTTTTTT[-/T]AAACATTTGAAGCAG | 79658 |
| rs200935036 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147836837 | AAGTATGATGTGCCT[A/G]TTTTTTTTTAAATTG | 79658 |
| rs200935817 | snp | C/G/T | 0.00199792 | 0.0315431 | ARHGAP10 | 4 | allele_origin=T(somatic)/C(germline) | 4:147906649 | TCAGGCCTGGCGTTT[C/G/T]CTTGACCATGCAGGC | 79658 |
| rs200950929 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148017678 | TATATATATATATAT[A/G]TATATGTGTGTGTAT | 79658 |
| rs200971384 | in-del | -/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147919577 | AAACAATTTTTTTTT[-/C]TTTTTTTTTTGTGGA | 79658 |
| rs200972105 | snp | A/G | 1.65023e-05 | 0.00287244 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147879303 | GCAAAGAAGTTCAAC[A/G]TGATCCCATTTGAGC | 79658 |
| rs200992418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147866832 | GTAAGGAAGTGAAAG[C/T]TTTCTTTATAAAAAG | 79658 |
| rs201008839 | in-del | -/ATATATATATAT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147912549 | CAAACAAACAAACAA[-/ATATATATATAT]ATATATATATATATA | 79658 |
| rs201010197 | snp | A/G | 0.000559975 | 0.0167235 | synonymous-codon, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147939844 | AAATGACCAAGGATT[A/G]TACAGAGTTGTGGGG | 79658 |
| rs201010898 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147953644 | TTTGTTTTCTCTCTT[C/T]TATTTCCTAATCATT | 79658 |
| rs201015180 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148049455 | GGGTCGTGCGTTGCT[A/G]TCCTCCCAGTAGCCG | 79658 |
| rs201022063 | in-del | -/TG | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147788137 | TTAAAAAATTTGATT[-/TG]TTTTTTTTTTAAAAA | 79658 |
| rs201050494 | in-del | -/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147983193 | GCTGCTTTGTTTTTT[-/G]TTTTTTTTTTGAAGC | 79658 |
| rs201059802 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148001650 | TTGTAAGTTGGATTC[C/T]AGGTATTTTATTCTC | 79658 |
| rs201078800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147899290 | TCTTGCTGCTCCACC[A/G]TGGATGAAAGCAGCT | 79658 |
| rs201082180 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147840791 | TTTGAGTCCCTCTCT[C/T]TAGCTCGAGAGCTCC | 79658 |
| rs201087083 | in-del | -/A | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147742480 | TCTGTGAACACTTTT[-/A]TTTTTTTTTTTTTTT | 79658 |
| rs201093171 | in-del | -/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147798150 | TACTTTTTTTTTTTT[-/C]GTAAGGGATACATTC | 79658 |
| rs201099432 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147771502 | AAAATGTATGATTAT[A/T]TTTGACTATAGTCAC | 79658 |
| rs201100184 | in-del | -/A/AA | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147882476 | CAAAAAAAAAAAAAA[-/A/AA]TTGCCTTGGAGCTTT | 79658 |
| rs201105697 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147897958 | TCCTGGGTTCACGCC[A/T]TTCTCCTGCCTCAGC | 79658 |
| rs201108372 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889670 | AGATACTTGTAAAGA[A/C]GACAAAGTATGTTTA | 79658 |
| rs201111144 | in-del | -/T | 0.00676609 | 0.0577691 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147915709 | TTTTCTTTTTGAATA[-/T]TTTTCCCCCCAAAGG | 79658 |
| rs201112760 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147926880 | GGGTTTAGTGGCTGG[A/G]AAGTCAAACTAGATA | 79658 |
| rs201120996 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148004269 | TCTCTCAAAATTTTG[G/T]AAAAATGCAAAGCAC | 79658 |
| rs201123646 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148014419 | CAAACCAGAAAACAA[A/C]ATTTTATAATTGGGG | 79658 |
| rs201124599 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147975201 | GTGGTAGAATGTGTC[-/T]TTTTTTTTGGTGTGA | 79658 |
| rs201149698 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147815730 | TAGGCGTGGTGGTGG[G/T]GGTTTCATGCCTGTA | 79658 |
| rs201178202 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147804011 | TTTTTTTTTTTTTTT[C/T]TTTCAGGTTCAGGGG | 79658 |
| rs201201854 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148071638 | AAACAAACAAACAAA[A/C]AAAAAAAAACACAAA | 79658 |
| rs201212040 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147924748 | CTTATTAACTCTGCC[C/T]GTAACCTCTCTGTGT | 79658 |
| rs201220481 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147741800 | CACACACGCACACAC[A/G]CACACACACACACAC | 79658 |
| rs201236418 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147989231 | GACAGACATCAAGTA[C/G]TTAACAGGGTAATAG | 79658 |
| rs201241757 | in-del | -/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147873888 | TTAAAAAAAAAAAAA[-/G]AGGGGGGATAAGAAA | 79658 |
| rs201248212 | snp | G/T | 3.30055e-05 | 0.00406222 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147939928 | CTAATCATTTTTCCA[G/T]GTGTTATTTGTGTAT | 79658 |
| rs201249811 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147920130 | TTTAAAAAACAACAT[A/C]ACCTCGCTGGGCACA | 79658 |
| rs201269477 | in-del | -/TATATATATATATATATA | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147798782 | CTCTCTCTCTCTCTC[-/TATATATATATATATATA]TATATATATATATAT | 79658 |
| rs201271675 | snp | C/T | 0.000296751 | 0.0121773 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148023269 | TGTTGGAAGATTTTT[C/T]GGACGCCGCCCGATA | 79658 |
| rs201273051 | in-del | -/TA | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147793163 | AAATGTGTGTGTATG[-/TA]TGTGTGTGTGTGTGT | 79658 |
| rs201312236 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147846556 | TGTGGTTGTGGCTGG[C/T]GTTTGTGTGTGTGGC | 79658 |
| rs201312262 | in-del | -/GT | 0.0126979 | 0.078662 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147744803 | GAGACATGTTCAATA[-/GT]GTGTTTCTTTTATGG | 79658 |
| rs201331003 | in-del | -/A | 0.00993419 | 0.0697739 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147959201 | CAAAACAAGATAGAG[-/A]AAAAAATGGTTTTAT | 79658 |
| rs201366567 | in-del | -/TGTC | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147899362 | GTGTCTGTGTCTGTG[-/TGTC]TTTGTCTTCTGTCCA | 79658 |
| rs201385493 | in-del | -/CCT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147914567 | GCGCTCCCCCCCCCC[-/CCT]TTTTTTTTTTAACAT | 79658 |
| rs201404112 | in-del | -/TTTG | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147791570 | TGTATATATATATAT[-/TTTG]TTTGTTTGTTTGTTT | 79658 |
| rs201413364 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148061176 | ATTTTTCAAGGGCCA[C/T]ATAAGTGTAGTCACA | 79658 |
| rs201419271 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147835489 | GAGATTTTCCTGCCT[C/G]AGTCTCCCTGAGTAG | 79658 |
| rs201421446 | snp | A/G | 4.94214e-05 | 0.00497074 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147881875 | TGAAAGAATGTACCA[A/G]GAGGCATACTGACTC | 79658 |
| rs201428517 | in-del | -/A | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148025594 | TATTTTACATATTCT[-/A]AAAAAAAAAGAAAAG | 79658 |
| rs201438853 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147866326 | TGGATGTGGCTGGGG[A/G]GAGCCTGGAGCTCTT | 79658 |
| rs201445690 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147905111 | AAATTTATTTGAGTT[C/G]ATTGTAGATTCTGGA | 79658 |
| rs201461109 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147874835 | GCTATTTTACTGCTA[-/T]TTTTTTTTTCTTTGC | 79658 |
| rs201461665 | in-del | -/AAATA | 0.0448719 | 0.142907 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147877244 | TTTTTTCTTAGAGTT[-/AAATA]AAATATCTGTGCAAT | 79658 |
| rs201478237 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147899891 | GTTTTTTTTTTTTTT[C/T]CCTTTTCAACATTCC | 79658 |
| rs201506757 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147838474 | AGACCCTTGTCTCTT[A/T]AAAAAAAAACACACA | 79658 |
| rs201507812 | in-del | -/G | 0.0130921 | 0.0798413 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147988172 | ACAGATGGAGCGTGT[-/G]TGTCTGGTCAACATA | 79658 |
| rs201516150 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147762526 | TTTATTTATTTTTAT[A/T]TATTTATTTATTTAT | 79658 |
| rs201550716 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148072091 | CTGTAGCTCCTGGCC[C/T]CAGAGCCCCTGCTGA | 79658 |
| rs201570264 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148054771 | GAGACCCAACCACAT[C/T]TATAACTTATTCTGA | 79658 |
| rs201591992 | in-del | -/ACTG | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147751438 | GCGTGATCTCGGCTC[-/ACTG]CAACCTCCGCCTCCT | 79658 |
| rs201592790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148062592 | TAACTTTAAAAAAAA[A/G]GGGAAATATTAAGAA | 79658 |
| rs201598931 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911997 | TAAGAACATTCACGT[A/G]TGTGTGTGTGTGTGT | 79658 |
| rs201600786 | in-del | -/AC | 0.238749 | 0.249747 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147783844 | TATTATATTTATATA[-/AC]ACACATTAAATTGTG | 79658 |
| rs201602224 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147988215 | AACTGGCTCTTTGAA[A/G]CCATTCAAACCTGAG | 79658 |
| rs201625840 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147737931 | TCAGCAATCTAATGT[C/T]CTCAGTGTCTTTTTG | 79658 |
| rs201636012 | in-del | -/TAAG | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147880706 | TTCTGCATTGCAAAT[-/TAAG]TAAAGATAAATTCAG | 79658 |
| rs201642310 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147939794 | AATATGATAGTCTTC[A/T]ATTTTGCTAATAGTT | 79658 |
| rs201643597 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147881133 | ACAAAAATTAGCCAG[G/T]CATGGTGATGCACAC | 79658 |
| rs201648313 | in-del | -/ATATATATATATATATATATATATAT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147766800 | CATACATATATTCAC[-/ATATATATATATATATATATATATAT]ATATATATATATATT | 79658 |
| rs201648903 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147817064 | ATTTGTCTATTTTAA[A/G]AAGGGCTATGGAATC | 79658 |
| rs201651288 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147922464 | GGAGGCCGAGGCGGG[C/G]GGATCACGAGGTCAG | 79658 |
| rs201653093 | snp | A/G | 0.143959 | 0.226396 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147839146 | TCTATCTATCTATCT[A/G]TCTGTCTGTCTATGT | 79658 |
| rs201654723 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147816592 | TGAGCTGCTTCTGGA[A/C]CAGCCTGTGATTTGG | 79658 |
| rs201656850 | in-del | -/TATA | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148043746 | ATGTGTATATATATG[-/TATA]TATATATGTATATAT | 79658 |
| rs201671375 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147853774 | AAGTTCTTATGGCTT[C/T]TTTCTTTCCTTTTTT | 79658 |
| rs201684124 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147989405 | CCAAAATTTATTAGG[C/T]GGGAATTTCCTCTTC | 79658 |
| rs201689268 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147912694 | AGGGTATTGCTCTGT[C/T]ACCCAGTGCAGTGGT | 79658 |
| rs201693197 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147925427 | TTGAGTTTGAGTCTC[-/T]TTTTTGATTTATTGT | 79658 |
| rs201701934 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147824364 | TCTATATTCTTGAAA[A/G]TGAGTACTATCTAGA | 79658 |
| rs201725215 | in-del | -/A | 0.0298908 | 0.118541 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148049010 | TCAGAAACTTGATTT[-/A]TTTTTTTCTGTGCCA | 79658 |
| rs201732542 | in-del | -/A | 0.0107246 | 0.0724382 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147812237 | AGGAAGTGGGGAATG[-/A]AAAAAAGAAAACATC | 79658 |
| rs201755887 | snp | C/G | 1.7093e-05 | 0.00292339 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147879185 | TATAGCTCTGCAAAT[C/G]TGCTTATTTATGAGG | 79658 |
| rs201761277 | snp | A/G | 6.16466e-05 | 0.00555153 | synonymous-codon, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147857579 | GAAGTTTGACAAAGA[A/G]ACAGAAAAGAATTAT | 79658 |
| rs201782289 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147959244 | AGTATTTTTTTTTTT[-/T]GTTTTTGAAGAAGAG | 79658 |
| rs201786763 | in-del | -/AC | 0.0850919 | 0.187897 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147784026 | TTATATAATTATATA[-/AC]ACACATTAAATTATA | 79658 |
| rs201813280 | in-del | -/ATATATATATATATATATATATAT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147912549 | CAAACAAACAAACAA[-/ATATATATATATATATATATATAT]ATATATATATATATA | 79658 |
| rs201829552 | snp | A/G | 3.29554e-05 | 0.00405914 | missense, utr-variant-5-prime, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147822745 | TGTCAGTGGCCCAGC[A/G]GAAGTTTGCTCATTC | 79658 |
| rs201833723 | in-del | -/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147855684 | TATTGTCAGATGGTT[-/G]TTTTTTTTTTTTTTT | 79658 |
| rs201834793 | in-del | -/A | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147851254 | AAGACTATGACTAAT[-/A]ATTTTTTTTTTTTTT | 79658 |
| rs201871737 | in-del | -/A/AA | 0.0248432 | 0.108648 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147824018 | ATTTATTTCAGGCTT[-/A/AA]AAAAAAAAACACAGA | 79658 |
| rs201896843 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147854442 | GCATTTCTCTCCCAG[A/C]CTGTTTCACTCATTA | 79658 |
| rs201914883 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147854064 | GGTTCTTAGGTTCTT[C/T]TCTTCTACCATTTAT | 79658 |
| rs201919036 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147841716 | CTTCTTTATTATTTT[G/T]TTCTTAAATATAATT | 79658 |
| rs201957372 | in-del | -/TATA | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147793235 | ATATATGTGTGTGTG[-/TATA]TATATGTATGGTAGG | 79658 |
| rs201959471 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911209 | GAAAACCACTGCCCA[A/C]TTCATTAAAATTCTC | 79658 |
| rs201988387 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147753600 | CTCAGGTGATCTGCC[C/T]GCCTCAGCCTCCCAG | 79658 |
| rs202014759 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147803752 | TCCATGTTGCTGTAA[A/G]TTACAGCATTTTATT | 79658 |
| rs202037215 | in-del | -/T | 0.00478085 | 0.0486577 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147798447 | AGGTGTGGTGGCTCA[-/T]TGCCTATAATCCCTG | 79658 |
| rs202042143 | snp | A/G | 9.90066e-05 | 0.00703516 | missense, utr-variant-5-prime, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147822937 | TTTTTGAAGAATCTG[A/G]AGGAACAGAGAGAAA | 79658 |
| rs202046229 | snp | A/C | 0.00199792 | 0.0315431 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148072010 | CAAACCTCCAGGGAA[A/C]CTGGCTGGCTAGAAG | 79658 |
| rs202057361 | in-del | -/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147776115 | CATTTATGGCCTCCT[-/G]CGTAATCATTAACTT | 79658 |
| rs202098692 | in-del | -/TGT | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148018756 | TCCCTAAGAATTAAA[-/TGT]TGTTTGTTTCATAAA | 79658 |
| rs202110380 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147915945 | CTGTCTGTATAAAAA[-/T]TTTTTTTAAAAAAAT | 79658 |
| rs202120441 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147983187 | GTGCCTGGCTGCTTT[G/T]TTTTTTTTTTTTTTT | 79658 |
| rs202124046 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911507 | AACTGGGACTACAGG[C/T]GCCCACCATCACGCC | 79658 |
| rs202134962 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147977653 | ACTCAATTGTGTGAC[-/T]TTTTTTTTTCCATTT | 79658 |
| rs202175179 | in-del | -/C | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147886186 | AATTGAAATCCAGAA[-/C]CCTTCTCATTGCAAG | 79658 |
| rs202180426 | in-del | -/ATATATATATATATATATATATATAT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148043615 | GAGACCCTCTCTCTA[-/ATATATATATATATATATATATATAT]ATATATATATATTTT | 79658 |
| rs202183626 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147989461 | AGACTGGAGTTTATT[C/T]CACCTCTGCAATCTT | 79658 |
| rs202203399 | in-del | -/A | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147832357 | TTTTTTTTTTTTTTT[-/A]AAAAGAGGAGTCCAG | 79658 |
| rs202211834 | snp | C/G | 3.29484e-05 | 0.00405871 | missense, intron-variant, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148063180 | CGTCTATGGTCCAGT[C/G]GCTTAACCCACAGTC | 79658 |
| rs202237328 | snp | C/T | 1.64961e-05 | 0.00287189 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147939917 | ATGCCTCTTTTCTAA[C/T]CATTTTTCCATGTGT | 79658 |
| rs202238537 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147882462 | AGTGAGACTCCGTTT[A/C]AAAAAAAAAAAAAAT | 79658 |
| rs267600033 | snp | C/T | | | synonymous-codon, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147906650 | CAGGCCTGGCGTTTC[C/T]TTGACCATGCAGGCA | 79658 |
| rs267600034 | snp | C/T | | | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148047008 | CCAGACAAAAACCAC[C/T]TTCTGGCAGATGGAG | 79658 |
| rs367553837 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147949694 | AACTTGACCAAGAGA[C/T]GTACTGCCACTCTAG | 79658 |
| rs367561901 | in-del | -/GC | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147861148 | GCCAGGCACGGAGTG[-/GC]GAGGAGTTCGTGAGT | 79658 |
| rs367573073 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147892814 | GCAATATCTGGAGAC[A/G]CTGATATAATGTATT | 79658 |
| rs367576486 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147924150 | TTCATTTTCACAATT[A/G]GTAATCTTATTTGTT | 79658 |
| rs367582896 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147871699 | TATTGTAATTAGAAG[A/C]TGCCTTCATATGTAC | 79658 |
| rs367587336 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147817164 | CTTTTTCTTTTCAAG[C/T]CCAGGATTATAGAAC | 79658 |
| rs367591544 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147822031 | TTTTGAATGAAATGA[A/G]ATGTGTATCACCTAG | 79658 |
| rs367601262 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147746855 | TCAACTGATGGATTT[A/G]TTTTCCCTGAGGTAG | 79658 |
| rs367610051 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147833023 | TAGGTCAAGGAAGTG[C/T]TGGTATCAGTATCCA | 79658 |
| rs367623990 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147793975 | GTTTAATTTTCAAAC[A/C]GTTCTACTATTCTTA | 79658 |
| rs367635119 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147946589 | ATCAAGGTTTTAATT[A/G]TTTTTTTCTTGTTTG | 79658 |
| rs367658666 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148037929 | ATCTCATATGCTGGC[C/T]GAAGCTTTTCACCAG | 79658 |
| rs367660659 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148013234 | GCAAATGGAAAAAAG[A/C]AAGTATTGGATTCTC | 79658 |
| rs367666348 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148071181 | AGCCACTGCACTTGC[A/G]AAGGCCTGGAGTTGC | 79658 |
| rs367674329 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147908128 | GGATTACAGGCATGA[A/G]CCACCACACCCAGCC | 79658 |
| rs367683793 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148026457 | TTAACTAAATAAACC[A/G]AGTGTCTTTACTTTA | 79658 |
| rs367686826 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147923136 | TTGGAATTGGTACTT[C/T]CACATAACATGTAGG | 79658 |
| rs367688246 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148053806 | TGTGGCTTGCTGGGG[G/T]ATTTTTGGTATCTGC | 79658 |
| rs367714286 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148001886 | TGACTTCCTCTTTTC[A/C]TAATTGAATACCCTT | 79658 |
| rs367723165 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147949096 | GATATAAAATTTATC[C/T]GTGGGTGATAGTTAT | 79658 |
| rs367728374 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148049918 | TGTCACCCAGGCTGG[A/T]GTGTGGTGGCATGAT | 79658 |
| rs367735977 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147969765 | CTGTTACAATAGTTA[C/G]AGCAGACGAAAGTGG | 79658 |
| rs367747223 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148005683 | TGAAGAAACTTTAAA[C/G]AGTGAATCTGATTCT | 79658 |
| rs367765418 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147742854 | CCTCTCATTTATACA[G/T]AGGAGAAATCATCCA | 79658 |
| rs367767110 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147919658 | GCTCAGTGCAGCCTC[C/T]GTCTCCGCCTCCCGG | 79658 |
| rs367769905 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147882615 | ACATTCATTTGTGTG[G/T]GGGGGGGTTTTCAGT | 79658 |
| rs367769946 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147928629 | AAATAATTATCATCC[A/G]GGGAAGAACTTACAA | 79658 |
| rs367781292 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147866644 | GGGGGAACACTTGGT[G/T]GTTTATATGATTCTT | 79658 |
| rs367785167 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147956937 | TCCTAAGAGGTAGGA[A/G]CTTATATCTTAAGAG | 79658 |
| rs367800150 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147832665 | AAAAAAAAAAAAAAA[A/G]GAAATTGGAGCTCAT | 79658 |
| rs367815500 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148056346 | CCAGACATTTTCCCT[A/G]TGGGTTTTGGATGCC | 79658 |
| rs367827782 | snp | A/G | 3.333e-05 | 0.00408214 | synonymous-codon, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147966827 | GGAAATCTTAATTGA[A/G]AACCATGAAAAGGTA | 79658 |
| rs367843010 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148011441 | GGCTCCCCTGGGACT[G/T]TTGAGCACGGCACCT | 79658 |
| rs367849718 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147959007 | AATTTAGTATCCTAG[-/T]TTTTTTTTTTAAGGT | 79658 |
| rs367875587 | in-del | -/C/CC | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148013120 | GCTGATACTAATCTG[-/C/CC]CCCCCCACCTTCAGG | 79658 |
| rs367883227 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148069285 | CCCACCTCGCCCACT[C/G]CTCAGCTGGGTCCAC | 79658 |
| rs367905669 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148072405 | CACCTGTGTCGCCTC[C/T]ACTGGCAGTCACGCC | 79658 |
| rs367913600 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147958068 | GGAAATTTATAAGAC[A/G]AAAATGTAGTTACCT | 79658 |
| rs367928904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148055994 | CAGGGGTGAGCAAAC[C/T]GTGGCCCACTGCCAC | 79658 |
| rs367946135 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148010228 | TGGAGATTCCAGATA[G/T]CTCTGGTCTGGTGCA | 79658 |
| rs367946341 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147890296 | AGCCATTACTACTTT[C/G]ATTATCAATGGTTAG | 79658 |
| rs367997475 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911438 | CGCAATTTCAGCTCC[C/T]TGCAAGCTCCGCCTC | 79658 |
| rs368009434 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147831017 | CATCACTTTAGGAAC[G/T]TGCAAGAAATGCACA | 79658 |
| rs368013057 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147780649 | CATGGAGAGGGACTT[A/G]AGAAGGGGAAGTCAC | 79658 |
| rs368031807 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147824218 | TCCCAGCTACTCGGG[A/G]GGCTGAGGCAAGAGA | 79658 |
| rs368035959 | in-del | -/TCT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147743774 | AAGAGTGAAACTCCT[-/TCT]CAAAAAAATAAATAA | 79658 |
| rs368043013 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147785682 | CTGCTTGAAGAAATG[C/T]ACTGCTAAGAGGACA | 79658 |
| rs368050786 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147762210 | ATCTGGTTTCACCAT[A/G]TTGGCTGGGCTTGTC | 79658 |
| rs368070329 | snp | A/G/T | 9.91267e-05 | 0.0070395 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148064421 | TTCTTTTCAGCATCC[A/G/T]CAGTCGGAAGGCTCG | 79658 |
| rs368072733 | snp | C/T | 1.64876e-05 | 0.00287116 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147939907 | GTTGATGGGTATGCC[C/T]CTTTTCTAATCATTT | 79658 |
| rs368083595 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148027500 | TGATGAGGATACAGA[A/G]CCTTCTCAGCAAAAA | 79658 |
| rs368091626 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147920158 | ACAGTGGCTCATGCC[C/T]GTAATCCCAGCACTT | 79658 |
| rs368101248 | snp | A/G | 9.0474e-05 | 0.00672524 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147875195 | GCTGCTTAAAAATGC[A/G]AATTATTGAAAACTC | 79658 |
| rs368111605 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147951058 | GCATAATACATTCTG[A/T]ATGGGGAACTTGTCA | 79658 |
| rs368125481 | in-del | -/CTT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148050683 | CGGTTGATTCATCTT[-/CTT]TCTTATAAAGATTAC | 79658 |
| rs368135231 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147981357 | TAGTTTCCATGTATT[A/T]GTGTGTTTTTTAGAG | 79658 |
| rs368142190 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147761336 | CTCTATATAGAGTTA[A/C]ATTTGTTTAAAATTT | 79658 |
| rs368147714 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147938638 | AATTCTTTAGACTCT[G/T]ACTAGTATTCTTTTC | 79658 |
| rs368149785 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147935007 | TGGGCAACCAGAATA[A/G]CACCTGGCACATATC | 79658 |
| rs368159750 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147914769 | TCCATTCACCTATTG[A/T]TAAATATTTGGGTTG | 79658 |
| rs368173121 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147973290 | GAGTCTAGTGACCTG[C/T]TAGCTTATGTCTGAG | 79658 |
| rs368174104 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147878921 | AGCTAAGACTATAGG[A/C]GCCTGCCACTATGCC | 79658 |
| rs368191267 | in-del | -/T | 0.228842 | 0.249103 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148061097 | TTCATGGAGGTTTCC[-/T]TTTTTTTTTTTAAAG | 79658 |
| rs368192933 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147893084 | TTTTTTTTGAGACGG[A/T]GTCTTGCCCTGTCCC | 79658 |
| rs368207439 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147957279 | TGTATTTTAGGGGCC[A/G]AGGTTTCCAATGTAG | 79658 |
| rs368213880 | in-del | -/AACCA | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147898869 | TGCCAAACACTTTTA[-/AACCA]CCAGATCTTGTGAGA | 79658 |
| rs368215945 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889362 | TGCAGTGCAATGGCA[C/G]GATCTCGGTTCACTG | 79658 |
| rs368217052 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147847078 | GTGGGATGGAAGAGG[A/G]AAATGAAATACTAAT | 79658 |
| rs368239462 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147868827 | AATCTGATGCCACCG[C/T]GGATCTGACAGAAGG | 79658 |
| rs368264167 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148050452 | CATCTCAGCTCACTG[A/C]AAGCTCCGCCTCCTG | 79658 |
| rs368266632 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147903014 | AAGGGGGAAGTCTAC[C/T]CCTATGATCAAGTCA | 79658 |
| rs368294694 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148031477 | ACATCTGTGACAAAG[C/T]TAGGATGGAACCCAG | 79658 |
| rs368304720 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147791112 | GTACATATTCTTTAC[-/T]TTTTTTTTTTTTTTT | 79658 |
| rs368310767 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147928368 | CTTACGTGCCAAACT[A/G]TCTGGTTTCTGTGTT | 79658 |
| rs368321969 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147747749 | ATGCTCATTTATTTC[A/G]GCTGTCAGTGAGAGG | 79658 |
| rs368327971 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148021014 | TTAGTCTTGGCTACA[C/T]AAAAGAATCACCTGA | 79658 |
| rs368342959 | snp | A/G/T | 0.000100019 | 0.00707111 | missense, utr-variant-5-prime, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147732428 | GAGCTCATTAAGGAC[A/G/T]GGAAGAACCTCATCG | 79658 |
| rs368353072 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147770258 | TAGCCTGTGGTCAGG[C/T]GCCAGTGGTTCACGC | 79658 |
| rs368353916 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147919970 | GATTCTTTAAATTTC[C/T]GCAGATGATTCTAAT | 79658 |
| rs368356732 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148043337 | CAACCTTTTTACCCA[C/G]AGGTGATTTGTCTGT | 79658 |
| rs368363296 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147953227 | GGTCTGTAGTCTTCT[C/T]ATAATGCCTTTCTCA | 79658 |
| rs368386104 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147961820 | ACTGGCTGTGCCCAG[A/C]CTTTGCAGATTTCTT | 79658 |
| rs368389421 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148010229 | GGAGATTCCAGATAT[C/T]TCTGGTCTGGTGCAC | 79658 |
| rs368399311 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147999537 | CCAGTGAGGCGCCCA[C/T]TGCCGCTCTGGATCA | 79658 |
| rs368406386 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147871074 | ACGCCATTCTCCTGC[C/G]TCAGCCTCCCGAGTA | 79658 |
| rs368411564 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148060025 | GAGAGAGGGGAGAGA[C/G]ACGAGAGAGAGACGA | 79658 |
| rs368422327 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147915603 | ATCTGGAGGCATTGA[A/G]TATGTTTTTATAAGT | 79658 |
| rs368429450 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147962252 | CTTCTTCCTTCTGAC[C/T]CACTGCTAGTCTGCT | 79658 |
| rs368434455 | in-del | -/AG | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147778101 | ACATGGGTTTGTGAC[-/AG]GGGAGATCCTGCTAG | 79658 |
| rs368477301 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147850849 | CCTTTTTGAGCTTGG[C/T]ACTTATTGCCAAATG | 79658 |
| rs368481148 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147877852 | TGAGATTACAGGCAT[G/T]AGCCACGAGGCCCAG | 79658 |
| rs368488295 | snp | A/G | 0.000307953 | 0.0124049 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147866827 | AGAATGTAAGGAAGT[A/G]AAAGCTTTCTTTATA | 79658 |
| rs368493536 | snp | A/C/G | 0.0123036 | 0.0774623 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147864249 | GACCAGCTGGTGCCC[A/C/G]CTTCTCTCCCAGGGG | 79658 |
| rs368498125 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147825574 | GTGTGAAGACAGTGT[C/G]GTCCCATGAGGTTTT | 79658 |
| rs368502034 | in-del | -/A | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147811644 | TCTTTTGAGGGGGGA[-/A]GCTTACCTTCTAAAC | 79658 |
| rs368540376 | in-del | -/TAT | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147906150 | GTATATTCATATGTA[-/TAT]TATTCCATATGAACC | 79658 |
| rs368553177 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148059281 | TTTCTGAGCTTTTTA[C/G]GAACAGTTGACTTCT | 79658 |
| rs368567553 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147819649 | GCCTCCCGGGTTCCT[A/C]CCGGGTTCACACCAT | 79658 |
| rs368568160 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147858166 | TATGTAAGCAGGAAG[A/G]AATTTATATTTTATT | 79658 |
| rs368582975 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147887039 | TGGGATTACAGGCGC[A/G]AGTCACCCTGCCCGG | 79658 |
| rs368599697 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147762741 | TTCACCGTGCTAGCC[A/G]GGCTGGTCTCGATCT | 79658 |
| rs368620543 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147832540 | TAATCCTAGCTACTT[A/G]GGAGGCTGAGGCAGG | 79658 |
| rs368643108 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147942846 | GATTTCCAGCAGCCT[C/T]TAAGCCTTTCCCTGG | 79658 |
| rs368647641 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147918720 | TGGGGAAATTTAATT[C/T]ACTATCACTGGGAGT | 79658 |
| rs368651435 | in-del | -/GA | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148060036 | AGAGACGAGAGAGAG[-/GA]ACGAGAGACAGATAT | 79658 |
| rs368659121 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147862140 | CTCCTGTGCTTGTTG[C/G]CATCCAAAGTCCAGA | 79658 |
| rs368662689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147874905 | TTTTGAGAAATTTAT[A/G]AAAAAGTTATTTAGA | 79658 |
| rs368669859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147858400 | TTATGTACTACTGTC[A/G]TAAACACTTATTGAA | 79658 |
| rs368671305 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147797703 | AGCATGAGCCGTTGC[A/G]CCTGGCCAGCCAACA | 79658 |
| rs368685839 | in-del | -/AAA | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147785083 | GGACGACTATTTTCT[-/AAA]AAAAAAAAAAAAAAA | 79658 |
| rs368687648 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147777023 | TGATCTGAGCAACCT[A/G]TGACTGGGCGTGTCC | 79658 |
| rs368688207 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147761550 | ACTTGATATTTGAAT[A/T]TATCTCTTTCTCTTT | 79658 |
| rs368699567 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147844882 | GAGTAATCTTGAAAA[A/G]CTCTAATTATCATTC | 79658 |
| rs368700845 | snp | A/G | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147770363 | AACCCTGTCTCTACT[A/G]AAAATGGAAAAATTA | 79658 |
| rs368703430 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147815607 | CACACCTGTAATCCC[A/G]GCACTTTGGAGGGCC | 79658 |
| rs368707168 | snp | C/G | 1.64781e-05 | 0.00287033 | missense, intron-variant, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148063242 | ACACCTCTTTCACCC[C/G]GGTCGTCCCCTTTCC | 79658 |
| rs368742255 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147987773 | ACAGAGAAAAGGCAG[G/T]GATGGGGAGAGAATC | 79658 |
| rs368743426 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147734321 | CAGTGCATCTGGGGG[A/G]CCAGATGTCAGCTTT | 79658 |
| rs368759877 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147900298 | AAAGAGGTTGAGATG[C/T]TGATTTATGAATTTA | 79658 |
| rs368760946 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147757591 | CCCTTTACCAGCTTT[A/C]CATCTGCTGTAGCAT | 79658 |
| rs368810013 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147741386 | TCTCAGGACTATATG[A/G]GAACTGGTTTGAGTC | 79658 |
| rs368831087 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147848105 | AGTTTTTTTTTTTTT[C/T]TCTTCCTAAAAGAAA | 79658 |
| rs368832238 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147774607 | CTTTATTTCCTGTGA[C/T]TTTGTTTATTTCATG | 79658 |
| rs368869915 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147817669 | TTGCCTGTGGATCAA[A/G]ACACAAAAATTCAAG | 79658 |
| rs368870577 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147885194 | TTTGGGTCATTGTAT[C/T]AGTTCATTTTCATAC | 79658 |
| rs368872753 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147853141 | ACACCAGCCTTGGAC[A/G]GGGCATGATCCCACA | 79658 |
| rs368874006 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147963295 | CCCTCAGTCCTGCCT[C/T]TCCTTGAACCCTTCC | 79658 |
| rs368875432 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147762697 | ACCACGCCCGGCTAA[-/T]TTTTTTTTGTATTTT | 79658 |
| rs368879709 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147996418 | TGTGATTGTCTTAAC[A/G]TGACCATCTCATACT | 79658 |
| rs368884353 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147898189 | GGCTGCCTTAGGCTG[A/C]ATTTCTTGTAATGCA | 79658 |
| rs368887795 | in-del | -/TGAA | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147921696 | CAAATGTGTTTTAGG[-/TGAA]TCCCAGACAGACTCA | 79658 |
| rs368893256 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147869631 | CTTAAGGATGTGGTC[A/G]TCAGTAAATCTCCCT | 79658 |
| rs368905999 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147895256 | TTCCAACTGGTCACT[A/G]TTAGCATGTAGAAAC | 79658 |
| rs368907424 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147992571 | CCACCAACCCCAGCT[A/T]ATTTTTGTATTTTTA | 79658 |
| rs368911996 | snp | C/T | 0.000165412 | 0.00909279 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147955418 | CAGTTTTGTAGTTGG[C/T]AGTGAGCATAAACGA | 79658 |
| rs368922345 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147952542 | CCATGTGCTTATTTT[C/T]CATTTATATATTTTC | 79658 |
| rs368930713 | in-del | -/TTCTTT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147843539 | TTTTTCTTTTTCTTT[-/TTCTTT]GAGACGGAGTTTCGC | 79658 |
| rs368934266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147958920 | GATTTGTAGTTACAC[A/G]ATTAAAATGCCTTTT | 79658 |
| rs368953247 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148002469 | TTTTCTATTGATTGG[A/C]ATAGTTTCAGAAGGA | 79658 |
| rs368972928 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147971825 | ATCTGACAGCAGGAT[C/T]TGCAGTAGGAAGTAG | 79658 |
| rs368983244 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147887038 | CTGGGATTACAGGCG[C/T]GAGTCACCCTGCCCG | 79658 |
| rs368996633 | snp | C/T | 1.66485e-05 | 0.00288513 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148064535 | GGGAGCTTCGTCTGT[C/T]AATCCTGTCCGCAGG | 79658 |
| rs369002596 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148034645 | CATCTGGCAATTAAT[A/G]ATGAACTTTCCTTCT | 79658 |
| rs369015038 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147922572 | GGGCGCCTGTAGTCC[C/T]AGCTACTTGGGAGGC | 79658 |
| rs369033877 | in-del | -/TGG | 0.0130663 | 0.0797647 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148063330 | GTGGAATGTGGAATA[-/TGG]TGGCAGCACACACAG | 79658 |
| rs369056506 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148022177 | TATACATGTGCAGAA[C/T]GTGCAGGTTCTGGGA | 79658 |
| rs369063060 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147993779 | CACAGTAGTAGGCCT[A/G]CAGAGGATATAATGG | 79658 |
| rs369074197 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148051851 | TGTCATCATATACTT[C/T]GTGTGCACTCACTGG | 79658 |
| rs369078409 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148069644 | TGCAGGTGAGACTAT[A/G]TTTGAGACTCTCTTA | 79658 |
| rs369097247 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148071277 | GCTCCTGGAGGGGCG[A/G]CTGGAGCCAGGTGCC | 79658 |
| rs369100235 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148012580 | CCCTTGTTTAGAAAC[A/G]TTTCGGTTGGATGGT | 79658 |
| rs369109767 | snp | A/G | 0.00011533 | 0.00759287 | missense, utr-variant-5-prime, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147822819 | GATGATGAACGATGC[A/G]TAGGTAATTAAACAT | 79658 |
| rs369119840 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147840289 | ACCTGGCTTTGCTCC[C/G]TTTAAGCAAATCAGA | 79658 |
| rs369120033 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147856947 | AACCTCCGCCTCTGG[A/G]GTTCAAGTGATTCTC | 79658 |
| rs369120874 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147985769 | TTTTCTCAGTGTGTC[C/G]GTCTCAGCGTCTGTA | 79658 |
| rs369136060 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147925744 | GATACTAGTAGAAGA[C/T]ACAAGACTCCTGGAT | 79658 |
| rs369141178 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911634 | CCCAAAGTGCTGGGA[C/T]TACAGGCGTGAGCCA | 79658 |
| rs369141320 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147738367 | CCATCCTGGCTAACA[C/T]GGTGAAACCCCATCT | 79658 |
| rs369148820 | in-del | -/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147963721 | GGTCTGAAATCAAGA[-/C]CGTTGGGAGGGCCGT | 79658 |
| rs369173132 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147979433 | TTTTGTGCCCATACT[A/G]TGCTGTTTTGGTTAT | 79658 |
| rs369176037 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148012170 | GGGATGTGCCTGACA[A/G]TGTGTCATTACTTCA | 79658 |
| rs369200368 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147905664 | TTTGAAGTCAGGTAG[C/T]GTGATGCCTCCAGCT | 79658 |
| rs369204520 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147931214 | TTATCCATTTTGCCC[A/G]GAGACAGCTGTCATC | 79658 |
| rs369211531 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148044882 | TGCCTGAAAATTGGC[C/T]CTTCTATTGGCGCTG | 79658 |
| rs369243527 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147768528 | GTAATTAAAGGTTGA[G/T]ATTTAATGAATTTTA | 79658 |
| rs369304895 | snp | C/T | 0.000183997 | 0.00958983 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148023219 | GTAACACACAGGTTT[C/T]TGTTCATGGTAAATA | 79658 |
| rs369305141 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147983021 | TAGTAGCTGGACTCC[A/T]GGTGTGCATGACCAT | 79658 |
| rs369312386 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148034803 | AGCTTCCTCAAAGTT[A/T]ATGGAAGACAGTTTA | 79658 |
| rs369317827 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147881502 | AATCATCCAGGTGTG[A/G]TGGTGCATGCCTGTA | 79658 |
| rs369330029 | in-del | -/TAGTTCATGCCATCCTTCTGCCTGTAGTCC | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147870174 | TCCTGCCTGTAGTCC[lengthTooLong]CACCTGCCACCATGC | 79658 |
| rs369338341 | snp | A/C | 0.000574683 | 0.0169414 | utr-variant-3-prime, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148072113 | CCCTGCTGACCCTGG[A/C]ACCCAGGGACCTGCC | 79658 |
| rs369342211 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147740087 | AGAGTCTTGCTCTGT[C/T]GCCCAGGCTGGAGTG | 79658 |
| rs369352746 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148030098 | TGGGATGAACATTTC[C/T]CCCTTTCTGTGGAGG | 79658 |
| rs369361227 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147745124 | GACAAGGCCATGCCA[C/T]AGAGAGGTCAAGTAG | 79658 |
| rs369372130 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148027904 | TTGGAAGTTTTTTTT[-/T]GCCTCTACCATTTAT | 79658 |
| rs369375864 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147992657 | GTGATCCACCTGCCT[C/T]GGCCTCCCAGAGTGC | 79658 |
| rs369399650 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147763397 | GCTCACTGCAACCTC[C/T]GCCTCCTGGGTTCAA | 79658 |
| rs369401397 | in-del | -/A | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148013538 | TAAAAATACAAAAAA[-/A]TTAGCCGGGCATGGT | 79658 |
| rs369403109 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147820885 | CGTGAACCACCACAC[A/T]GGCCATATTTTACAT | 79658 |
| rs369406374 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147809505 | AACATGTAAACTCCA[A/G]TATTGGTTCTAGGTT | 79658 |
| rs369411465 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147770625 | AAAAGTAATCAGTAT[A/G]TATTGAGCACTTCTT | 79658 |
| rs369416341 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147831537 | TCTGTTGGCAGGCAC[A/C]TTCAGAATGGAGGAA | 79658 |
| rs369427950 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147845190 | GGTTTTAGCTTAAAT[A/G]TCACTACTTTGAAGA | 79658 |
| rs369440009 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147771899 | CAGGTTCTAGCGATT[C/T]TCCTGCCTCAGCCTC | 79658 |
| rs369465113 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147876358 | AGCACTCTGGGAGGC[C/T]GAGGTGGGCAGATCA | 79658 |
| rs369503939 | snp | A/G | 0.000395772 | 0.0140616 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147955342 | AGCCTCTCATGACCT[A/G]TGAGTTACATGGAGA | 79658 |
| rs369518623 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148045930 | GTCACATTTGCTTCC[A/T]TAGCAGTTTAGGACC | 79658 |
| rs369537451 | in-del | -/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148029998 | AGGCTCAGCATCCCC[-/C]CCCCCCACCAACCCC | 79658 |
| rs369543432 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147868191 | TCTAGTCACCCCAAA[A/G]TTGTCCCTGCAGGTA | 79658 |
| rs369550623 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148019713 | CAAGCCGAGCTGAGC[C/T]GAGATCGCGCCATTG | 79658 |
| rs369570177 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147838854 | ATTGTAACTAAATAT[C/T]TTAAATTTCTTAGTG | 79658 |
| rs369574938 | snp | C/T | 1.65677e-05 | 0.00287812 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148046889 | TGCTTTTTTTCCTCC[C/T]AGGTGACAATCCTTA | 79658 |
| rs369578975 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147925218 | TCAGAAGCCAAACAA[A/G]CACCACAAAACACCC | 79658 |
| rs369580470 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147999715 | CATTCGTTGGAATCC[A/G]TGAGGCCAAGAACCC | 79658 |
| rs369581387 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147887884 | AAAAAAATTTTTTTT[G/T]TCCTATTTCTTCCCT | 79658 |
| rs369583515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147860352 | GAGGCTGAGGCAGGA[A/G]AATGGCGTGAACCCA | 79658 |
| rs369585981 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147835103 | GAGAATCCCACTTCA[A/T]TTATAAATATTTTGA | 79658 |
| rs369589630 | in-del | -/AATT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147768589 | TGAACATAATGAAAT[-/AATT]GTTCATTTTTCAAAA | 79658 |
| rs369592485 | in-del | -/TTTG | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147753677 | ATTTTCTTATGTTTG[-/TTTG]CAGTGAACAAGTAAT | 79658 |
| rs369592755 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147861250 | ACAGGCACTGGCTCC[C/G]TGCAAGGCTGTGGCT | 79658 |
| rs369593227 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148013544 | ATACAAAAAATTAGC[C/T]GGGCATGGTGGCGGG | 79658 |
| rs369599469 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148046783 | CAGGCTGAACTGTAA[A/T]TGTAATTTTATCATT | 79658 |
| rs369604849 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147860678 | TCTATTTTTTCTTCC[C/T]AAGTAGCCAAATGAT | 79658 |
| rs369640966 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147843901 | CTTTCATTTCCTGAT[C/G]TGAGTACTTGGTCTG | 79658 |
| rs369650639 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147801568 | TGTAAAATAACATAC[C/T]GTCTGTTTTTTACTA | 79658 |
| rs369661175 | in-del | -/AC | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147741767 | GATATCGTTCTCTTT[-/AC]ACACACACACACACA | 79658 |
| rs369673977 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148068674 | AAACACAACATTCAA[A/G]CTACTGGTTGCCTCG | 79658 |
| rs369689847 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148054800 | GAGCCGTATACCCAG[A/G]TAGCTCACCCATTAC | 79658 |
| rs369698752 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147853349 | TGATGCTATTCAAGG[A/C]CCTGCCATATTTAAG | 79658 |
| rs369723520 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148028454 | TTAGCTACAAAATCA[A/G]GGTAATAATAGTATC | 79658 |
| rs369731591 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147955776 | GATTTGGAGAGATTA[A/G]TAGTTTGGAGGTGGC | 79658 |
| rs369753330 | snp | A/G | 1.66341e-05 | 0.00288388 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147879364 | GATTCAACATAGAAT[A/G]GATTATAATCTGTCA | 79658 |
| rs369774339 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147865447 | ACATTTCTTTTTACT[C/T]ATATTAGAAACACAT | 79658 |
| rs369774769 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147806846 | AGCTGGGACCACAAG[A/T]GTATGCCATCCTGCC | 79658 |
| rs369805263 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148002262 | ATCCCAGGGATGAAG[C/T]CCACTTGATCATGGT | 79658 |
| rs369810701 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148038211 | GTTTCTTGGTACTAG[A/G]TACCACTCTCCTTTT | 79658 |
| rs369812368 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147984499 | TGGCCTTTGGAGGCT[A/G]TGCTCCCACCTCCCT | 79658 |
| rs369850129 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147795052 | TTGTGGCTTTCTTTG[C/T]AAGGTAGCAGCTGCC | 79658 |
| rs369931576 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147782054 | GTGACCTTGCCTTGC[A/G]AAGGGGTAATATAGC | 79658 |
| rs369952929 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147904716 | TGTGTCTTTATAGCA[A/G]CATGATTTATAGTCC | 79658 |
| rs369953865 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147909523 | CTTGTTATGAATAAC[A/C]AAAGATGTTCTTATT | 79658 |
| rs369957222 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147862902 | TAACTGCTGATGGCT[G/T]AACTATCAAACTCTG | 79658 |
| rs369963730 | snp | A/T | 3.4353e-05 | 0.00414431 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148071949 | CGGCAAGAGGGGGC[A/T] | 79658 |
| rs369967867 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147815060 | TCATTAGGTTGAGAC[C/T]TCTGAGTCTCACTAG | 79658 |
| rs369968982 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147733739 | GTTGAAGTACATTTC[A/T]GTGGGAAGAATTTAG | 79658 |
| rs369974815 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148027861 | AAATGTAGATTTTTA[A/G]TTCTAAACGATGGAA | 79658 |
| rs369979897 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148069865 | TTTGCATAGAATCCA[A/G]AGCTTTTCCCTGATG | 79658 |
| rs369994384 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147837535 | TTGCTACTGGATGTG[G/T]ACACTACAGTTTGCA | 79658 |
| rs369996846 | snp | A/G | 3.29544e-05 | 0.00405908 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147822833 | CATAGGTAATTAAAC[A/G]TGATATTTTGGTTTG | 79658 |
| rs370005689 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147990010 | CACATTCTTCTGTCA[C/T]GGCTTCAGCTGGTCC | 79658 |
| rs370014432 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147897603 | ATATCTGCCTTCTCA[A/G]AAATAAAGACCCTTA | 79658 |
| rs370017127 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148020573 | ATTCCTGCATTAGTG[A/T]GCTGAGGATAATGGC | 79658 |
| rs370023415 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147761823 | TGATTTTAAAGACGG[C/T]ATTACTAGGAAAAAC | 79658 |
| rs370044058 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147814984 | AGCACCCATTAAACC[A/C]GGCTTTCTTGGCGTC | 79658 |
| rs370073589 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147828558 | TTTCCAACATGCTTC[A/G]TGGTAATCAAGTGAT | 79658 |
| rs370085054 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147789263 | TTCTATTTAAGTGGG[C/T]TGAGGGCCACTTGGT | 79658 |
| rs370106780 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147819949 | GGGAAATGAGGTTCC[A/G]GAGTGGGAAGATAGG | 79658 |
| rs370116615 | in-del | -/A | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148026665 | TAGTTTTCTTAAATT[-/A]AGAGCAGCTGTTAAA | 79658 |
| rs370134187 | in-del | -/AGAT | 0.00993419 | 0.0697739 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147935344 | GGTTTGAAAATAAAA[-/AGAT]AGAAGACAGTGTTCA | 79658 |
| rs370138164 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147917523 | CACATTCTACTAATC[A/C]TCCTTAATTCAATCA | 79658 |
| rs370150818 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148034342 | TTATTTTTTTGAGAC[C/G]ATTTCGCTCTTGTTG | 79658 |
| rs370158042 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147746304 | AGACGAGGTTTCACC[A/G]TGTTGGCCAGGATGG | 79658 |
| rs370158372 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147842235 | GCCACCATGCCTGGC[C/T]GTGAAACCCTTATAT | 79658 |
| rs370160800 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148051148 | AACAATGCAGCAGAA[C/T]TGGATTCCTTGGATT | 79658 |
| rs370170458 | in-del | -/GAGGG | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147938211 | TACTGAGGCCTATGG[-/GAGGG]TGGAGGGTGGGAAAA | 79658 |
| rs370181836 | in-del | -/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147827476 | CCTAAGCTTGTGGCT[-/G]GTTAGGAAAGGGTTT | 79658 |
| rs370183517 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147775173 | TCGCCTCGGCCCCCC[A/G]AAGTGCTGGGATTAC | 79658 |
| rs370188163 | in-del | -/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147959524 | CCTCCCCGCTCCCCC[-/C]ACCCCACGACAGGCC | 79658 |
| rs370189039 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147858071 | TATTTAATGCTGAGG[A/T]TTCAGGAGGTTCAAC | 79658 |
| rs370195034 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147870773 | AAGAAGAGACTAGAA[C/T]AGAATTCTTCCTGGA | 79658 |
| rs370195673 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147805125 | TTACATTGAAGTCTT[C/T]AATTCATCTTGAGTT | 79658 |
| rs370196666 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147842779 | TCTGCCACGTCATAC[G/T]GTGCTGACGTGTTCA | 79658 |
| rs370203901 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147823118 | CCTGATTTCTAGTTC[C/T]TTGAGGGTGCTGACC | 79658 |
| rs370204680 | snp | A/G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147912588 | ATATATATATATATA[A/G/T]ATATATATATAAAAT | 79658 |
| rs370218018 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148005493 | GTATCAGTATTATCA[A/G]TTATTATGGCCCTTT | 79658 |
| rs370220272 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147961058 | GCATTTTTCCTGGTT[A/T]TATACCTACGAGTGG | 79658 |
| rs370221992 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147926977 | GTATTATCCCCATTC[A/G]CATGAGCCCCTGAAG | 79658 |
| rs370225120 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147753534 | TTTTTTTTTTTTTTT[A/T]GTGGAGATGGAGTTT | 79658 |
| rs370226529 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147753141 | AAATACTGAATTTAG[C/T]AAACCTCAATTTGCG | 79658 |
| rs370228396 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147792379 | CCTCTTCCTTCCCTC[C/T]TTCTTTATTGGTGAC | 79658 |
| rs370246852 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147741140 | TTTGTTAATTGATGT[C/T]CTATGATGATGTACC | 79658 |
| rs370253581 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147976735 | TTCTGCTGTCATGTG[A/G]CTCTGTAAATGGTAG | 79658 |
| rs370270712 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147975495 | ATTTCTTACAGTTGC[A/G]TAAGCTGGAAAGCCC | 79658 |
| rs370275574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147803423 | GTAATTGGGATATCT[A/G]TTGCCTCAAACATTT | 79658 |
| rs370293555 | in-del | -/TTC | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889164 | CAGTCAACTATCCTT[-/TTC]TTCTGCACCACACCG | 79658 |
| rs370296283 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147942282 | ATTTGAGAAACAGTC[C/T]CAAGCCATGTACTAT | 79658 |
| rs370308753 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911723 | ACAGATATGCCAGCC[-/T]AATCATAGATAAGCA | 79658 |
| rs370338540 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147900027 | TTAGACTTGTGAATG[A/T]TTCTCTCTGCTTTTT | 79658 |
| rs370340384 | snp | A/G | 5.02828e-05 | 0.00501387 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147966832 | TCTTAATTGAAAACC[A/G]TGAAAAGGTAAAATT | 79658 |
| rs370346836 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147996356 | GTGGGAAAGATGAAC[C/G]CTGAGATAGAGGGGG | 79658 |
| rs370347699 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147985678 | GCCAAATTGCTGAAG[A/C]ATGACTGCCTTGTTT | 79658 |
| rs370366480 | in-del | -/ATA | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147784804 | ATATATATTATAAAT[-/ATA]ATATATTATAAAATA | 79658 |
| rs370374370 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147940229 | CAGAATTGTGACAGT[A/G]CATTTGGTTGGACAA | 79658 |
| rs370374999 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147895859 | GTGTTCATTATTTAA[A/G]GTGTAATATTAGCTG | 79658 |
| rs370383650 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147867757 | TAATCCCAGTTACTC[A/G]GGAGGCTGAGGCAGG | 79658 |
| rs370397514 | snp | A/G | 3.30022e-05 | 0.00406202 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147939927 | TCTAATCATTTTTCC[A/G]TGTGTTATTTGTGTA | 79658 |
| rs370397605 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147929214 | TGCTTAGGAATTATC[C/T]CTTACCCTGCTGCTT | 79658 |
| rs370413442 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148071825 | TTGTGGTGGCCAGTG[A/C]AGGGAGGCAGAGCCT | 79658 |
| rs370422245 | snp | A/C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147856636 | AGAAATGAATTTCAC[A/C/G]TTTAGACTTAGGCCC | 79658 |
| rs370442649 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148072552 | GCTTGGAGAAGCTGC[C/T]GTTGGTGCAAGGGAG | 79658 |
| rs370445181 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148054105 | ATTTTCTTACTTGAT[A/G]CCATTGTTGTAATTT | 79658 |
| rs370456591 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147876810 | CTGTGCTAAATTCGT[A/G]TACAACTTGTCTCAT | 79658 |
| rs370456785 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147786121 | AAGACAGGGGGAGAC[C/T]CTGGGCTGAGGAGCT | 79658 |
| rs370476644 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147987032 | TAACGGGATTATTGC[A/G]GATTGAACTGAATCA | 79658 |
| rs370485525 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147785567 | AGGACATAAATGACA[C/T]GTAGTTTATGCTTTC | 79658 |
| rs370487043 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148024848 | TCTGATGGAAGTGTT[A/G]ATAAATAGTGAAATA | 79658 |
| rs370488141 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147751673 | ACCTGGCCTTTTTTT[-/T]GCTTTTTTTGGAGCA | 79658 |
| rs370532827 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147754114 | ACAGTGCCTTGCTCA[A/C/T]AGGCACTGAGTCAGT | 79658 |
| rs370536052 | in-del | -/AAAAC | 0.0682035 | 0.17161 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147860436 | GACAGCTCCGTCTCA[-/AAAAC]AAAACAAAACAAAAC | 79658 |
| rs370541915 | snp | A/G | 4.9445e-05 | 0.00497193 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147864871 | AAGTAGAGCAGAACC[A/G]GCAACACTTCTATGA | 79658 |
| rs370549475 | snp | C/T | 0.000116106 | 0.00761838 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148047061 | CACTATGTAAGTAAC[C/T]GTGCTTCTGTTGGGT | 79658 |
| rs370550102 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147755408 | ACAGGAAGGGACCCT[A/T]GCTACTCGGGAGGCT | 79658 |
| rs370567368 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147915129 | ACAGGACTGCCACCT[A/G]TGAAACTAGTGTGTA | 79658 |
| rs370584524 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147902838 | GGCCTCAGGAAACTT[A/G]TAATCATGGCAGAAG | 79658 |
| rs370596826 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147994001 | GCAAGAAAATGAAGC[A/T]TGGAGAGCTGAAATT | 79658 |
| rs370612219 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148032272 | TCATGGGTTGAACCA[C/T]ATAAAATTGCCATCT | 79658 |
| rs370613937 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147737326 | AGCTAATTTTTGTAC[-/T]TTTTTTTTTTTTTTT | 79658 |
| rs370621662 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147744665 | GCTGCCCTGACACCT[A/C]AGGTTCTGGTGTGGG | 79658 |
| rs370644272 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147735690 | CACATTTGTGTGTAG[A/G]GTGAAGTTGGGGATA | 79658 |
| rs370652594 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889669 | GTAAACATACTTTGT[C/T]TTCTTTACAAGTATC | 79658 |
| rs370664553 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147747103 | CCGCTGTTTCAGGCT[C/T]TATTTCACACTTTGT | 79658 |
| rs370692702 | snp | A/C | | | intron-variant, downstream-variant-500B | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147782866 | TTTCATATATATATA[A/C]AAACAACATAAAATA | 79658 |
| rs370700874 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148055197 | TTTGCTCTAAGAGAG[G/T]GGACTTTGGGAGTGA | 79658 |
| rs370738046 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148037703 | AGCTGGGTGTGGTGG[C/T]GTGTGCCTGTAATCC | 79658 |
| rs370745052 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147920643 | AACGTTGGTTACATA[A/C]AATCCTTGATTTATT | 79658 |
| rs370759039 | in-del | -/AAAA | 0.142875 | 0.225886 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148071644 | AACAAACAAACAAAC[-/AAAA]AAAAACACAAAAAGC | 79658 |
| rs370760462 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147950714 | GGCAATTTTTTTTTT[-/T]AACTTCTCATGTTTT | 79658 |
| rs370767595 | in-del | -/GACGTGA | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147736860 | ACCAAGGAGACGTGA[-/GACGTGA]CAGGAAGTCTGGGTA | 79658 |
| rs370769849 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147905967 | CCTTGTAAGTTGGAT[A/T]TCTAGGTATTTTATT | 79658 |
| rs370775139 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147948679 | AATGCATTGTAGGCC[A/G]GGCGCGGTGGCTCAC | 79658 |
| rs370784860 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147853847 | TCTCTATGGCTTCAT[G/T]GTTTACTTGTGACTC | 79658 |
| rs370787094 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147789545 | TCCCAAAGTGCTGAT[A/T]ACAGGCGTGAGCCAC | 79658 |
| rs370797877 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147816129 | GTCGCCAGCATTCTC[G/T]TCCTATCTCCCATCC | 79658 |
| rs370800661 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147898084 | GGCCATATTTTTTTT[-/T]AACACTAACGTATTT | 79658 |
| rs370818170 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147850465 | CAGCTTCACTCCTGA[A/C]GCCAGGAGACCATGA | 79658 |
| rs370820937 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148008145 | CATACAGTCTCCATT[A/G]CTTGTCTTGTGTAGC | 79658 |
| rs370822996 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889368 | GCAATGGCACGATCT[C/T]GGTTCACTGCAACCT | 79658 |
| rs370837043 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147812819 | ATCTGACTTCTGTGC[C/T]CCTTCTTATGCTTGT | 79658 |
| rs370853201 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148048615 | GTTACACTCGAGGTG[A/G]AATTTAGCATGTGTG | 79658 |
| rs370853738 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147774025 | CAGCTTTGTGATCTC[A/G]GGCAAGTTACCTCTC | 79658 |
| rs370858812 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147867112 | ACAGACAAAAGAGCA[C/T]TCCACTTTAAGGCAT | 79658 |
| rs370860233 | snp | A/C/G | 4.94868e-05 | 0.00497407 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147966717 | AACCTGATGACTGTG[A/C/G]CAAACTTAGGAGTGG | 79658 |
| rs370880919 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147829455 | CGATCTCTGAAAGTG[C/T]TGGGATTACAGATGT | 79658 |
| rs370888990 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147764361 | CAGGAGAGAGGTGGG[G/T]CAGTAAACAGCACCT | 79658 |
| rs370913502 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147919569 | TCTTTTAAAAACAAT[G/T]TTTTTTTCTTTTTTT | 79658 |
| rs370929604 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147759558 | CCACCACACTCCTGC[C/T]TGGGTAGCATAGTGA | 79658 |
| rs370933992 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147902821 | GGAGGCATGGGTGGG[A/G]AGGCCTCAGGAAACT | 79658 |
| rs370935329 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147938215 | GAGGCCTATGGGAGG[C/G]TGGAGGGTGGGAAAA | 79658 |
| rs370942760 | snp | G/T | 1.67492e-05 | 0.00289384 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147847210 | CAGAAAAGAGCAACT[G/T]GGAGCTGTAAAGGTT | 79658 |
| rs370953344 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148047138 | AGCAGTGACCTGTGG[A/G]TGCTGAAGCCATTAG | 79658 |
| rs370953588 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148000673 | TGCATTTCTCTGATG[A/G]CCAGTGATGATGAGC | 79658 |
| rs370969122 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147735025 | TTGGAAGATTTCAAT[A/G]TGTAATTTTGATGGC | 79658 |
| rs370971249 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147863668 | AATTTATTTTAATTT[A/T]TTGCTGGGAGTTGTG | 79658 |
| rs370985475 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147784533 | ATATATAATATAAAA[A/C]ATATATTTTATAGTA | 79658 |
| rs371000989 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147895641 | CAGTGAGCCATAATC[A/G]TGTCACTGTACTACA | 79658 |
| rs371005513 | snp | A/G | 3.36967e-05 | 0.00410454 | synonymous-codon, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147965127 | GGTGAAACACTTAAC[A/G]AAGTAAGCCTCTTTT | 79658 |
| rs371009119 | snp | C/T | 3.46632e-05 | 0.00416298 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147847245 | TCTAATTTGAATACA[C/T]TCAGAAAACATAGAT | 79658 |
| rs371011736 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147933714 | GTCCAGAAGACTGTT[A/C]TAGTGGCCCAGATGG | 79658 |
| rs371024660 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147765192 | AGGCATAATTTATCA[C/T]TGTGAGTCATTTAAG | 79658 |
| rs371032470 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147741399 | TGAGAACTGGTTTGA[A/G]TCAGAAACAAAAAAT | 79658 |
| rs371037189 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147760417 | AACGTCAGGGTTTGA[A/C]TCCAGCAGCTCCCGT | 79658 |
| rs371042486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148071814 | GTAGATGAGGATTGT[A/G]GTGGCCAGTGCAGGG | 79658 |
| rs371066279 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148013074 | AAGCAAAGTGTTCCT[A/G]TAAATTTTAGAAACA | 79658 |
| rs371067229 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147815727 | CGATAGGCGTGGTGG[G/T]GGTGGTTTCATGCCT | 79658 |
| rs371069406 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148035735 | CTCAGTGCACCTGCC[C/T]GTGCTGAGAAACACA | 79658 |
| rs371085652 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147981684 | ATTATTATGTGGCTG[G/T]CAAAGTATTCTCTTA | 79658 |
| rs371086022 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147948033 | GCAACCTCCGCCTCC[C/T]GGGTTCCAGCAATTC | 79658 |
| rs371091161 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147942659 | CTTCTCCCCTAATTC[A/C]CAGCTGGCATGAAAT | 79658 |
| rs371096735 | snp | C/T | 4.95086e-05 | 0.00497512 | synonymous-codon, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147913075 | ACTGTTTCTTGTAGA[C/T]GCACAGTTGGATAAG | 79658 |
| rs371100013 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147851256 | GACTATGACTAATAA[A/T]TTTTTTTTTTTTTTA | 79658 |
| rs371133894 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147842143 | ATTTCACCATATTGA[C/G]CAGCTGGTCTCAAAC | 79658 |
| rs371139652 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147802521 | GGGCCCCCTTTGGAC[C/T]ATGTTTGTAGCCTCT | 79658 |
| rs371149907 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147972974 | TGGCCAGGCTGGTTT[C/T]GAACTCCTGATCTCA | 79658 |
| rs371153785 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147765743 | AATTTGAGGCTGCAG[C/T]GAGCCATGATTGCAC | 79658 |
| rs371154481 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148008424 | AAGCAATTTTGGCCC[A/G]AAGGGGACATTTGGT | 79658 |
| rs371155697 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147949515 | AGTGCTCCTGGCATC[C/T]GGTGGCATCTGACAT | 79658 |
| rs371161032 | in-del | -/A | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148037833 | GTGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 79658 |
| rs371180090 | in-del | -/GA | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147757023 | AGAGAGAGTGAGAGC[-/GA]GAGAGAGAGAGAAAT | 79658 |
| rs371189441 | snp | C/G | 0.000115774 | 0.00760748 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147866701 | ATATCTCTTTTCTTC[C/G]TGTGTCTTAGATGCT | 79658 |
| rs371196077 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147741769 | ATATCGTTCTCTTTA[C/T]ACACACACACACACA | 79658 |
| rs371204219 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147837641 | TAGAATCTCTGGTCA[C/G/T]TGTTTTTTTTTTTTT | 79658 |
| rs371219890 | snp | A/G | 9.8894e-05 | 0.00703116 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147939782 | GATGGCTTTTAAAAT[A/G]TGATAGTCTTCTATT | 79658 |
| rs371236651 | in-del | -/GGA | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147892193 | TTGAGGAAGAGAGGA[-/GGA]AATCACCTATGTATC | 79658 |
| rs371239074 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148067745 | CAGAGTGACCCCTGG[A/G]CGGCCTCGTCAGTAG | 79658 |
| rs371240632 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148054131 | AATTTATTATTTGCT[A/G]TTCATAAATTGGCTG | 79658 |
| rs371245988 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148064226 | AAAGGCTTGAATTGG[A/T]AACCCATCATTTACT | 79658 |
| rs371247186 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147793529 | GACCTGGGATCTCCC[C/T]GCATAGCTATTTAGC | 79658 |
| rs371313769 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147752648 | TTCTTGTGCCTCAGC[C/T]TCCCGAGTAGCTGGA | 79658 |
| rs371323558 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148016995 | TATTAAAAAAAAAAA[A/C]AAAAAAAAAACCAGC | 79658 |
| rs371331178 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911613 | GTGATCCGCCCACCT[C/T]GGCCTCCCAAAGTGC | 79658 |
| rs371340686 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147958962 | AGCTCCTAATTCCCT[G/T]GCATATTTCAAGAAT | 79658 |
| rs371345073 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147766450 | AAAAAAGTCAGTATG[C/T]AAGCAACCATCAGTT | 79658 |
| rs371348656 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147878022 | TCTCACTGCAACTTC[C/T]GCCTCCTGGGTTCAA | 79658 |
| rs371354679 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148057130 | CCTTCTCAGCATAGC[C/G]TCTAGCTATTGACAA | 79658 |
| rs371356908 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147892376 | TGTATAACACATTAA[C/G]TGTACTAATATTTGT | 79658 |
| rs371360779 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148070648 | GGAAGGCATTGCATG[C/T]GCGCAGTGAGGGTAA | 79658 |
| rs371361237 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148064360 | GGTTGGGGGGTGAAG[-/T]TTCTCTCTGTTTTCC | 79658 |
| rs371361290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147884522 | CCACCTTTTAGCTTC[C/T]GTCTTTTTTCTTGCA | 79658 |
| rs371366727 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147836068 | TTACAGGTAGATTGT[A/G]TTTGATTTAAATAAT | 79658 |
| rs371374331 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147813918 | TCTGCAATTTAAAGT[C/G]ATATAAATTTAACTC | 79658 |
| rs371377925 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147794056 | TGTGTTGTGAAGGAT[A/G]CAAAGACTGCCAAGT | 79658 |
| rs371415495 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147960226 | TGATAAATTTAGTTT[A/G]TATCTAGAAGTTTTT | 79658 |
| rs371416941 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147924195 | AGAAACTATTTGTTT[A/C/G]CAAATGAATGGTCAC | 79658 |
| rs371436489 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147778824 | GTGGTACAGGGAATG[A/C]ATTCTGTTGGAGGCC | 79658 |
| rs371473394 | in-del | -/G | 0.41833 | 0.184838 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147787452 | TGGAGTGATGGAAGC[-/G]GGTGGGGGAGGAGGC | 79658 |
| rs371485074 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147970886 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 79658 |
| rs371511251 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148043825 | CAGAAGTTGTTGAAC[A/G]TAGAATATTTTTTAA | 79658 |
| rs371521454 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147877265 | AATATCTGTGCAATA[A/T]TTTTTTTGTCAACCA | 79658 |
| rs371530116 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148052964 | GCTGGTGGTTGAGGC[A/T]GCAGAAAAAGTATTA | 79658 |
| rs371535865 | in-del | -/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147777262 | GTAGGGTGTGATTTT[-/C]TTTTTTTTTTTTTTT | 79658 |
| rs371544408 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911533 | ACGCCCGGCTAATTT[A/T]TTGTATTTTTAGTAG | 79658 |
| rs371546630 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889144 | AGATTCAATCAAGCA[A/G]CTGTCAGTCAACTAT | 79658 |
| rs371574432 | snp | A/G/T | 0.000183624 | 0.00958021 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147879228 | GGCTGTTTTTTTGTT[A/G/T]AAGGGCCTGCTCCGT | 79658 |
| rs371580528 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147810065 | TTATAGAGATTTTCA[A/G]TTTCTTATAGCAGCT | 79658 |
| rs371590691 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147913533 | GGCTTGCAGGTGGCC[C/T]CCTTCCCGCTTTGTC | 79658 |
| rs371591903 | snp | A/G | 0.000942873 | 0.0216921 | synonymous-codon, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147875062 | GTCAGAAGTGGAAGA[A/G]CTCATGAACAAAATC | 79658 |
| rs371595022 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147904358 | TTTAGCATTAGGTAT[A/G]TCTCCTAATGCTATC | 79658 |
| rs371606629 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147839512 | TTAGTAGTTATACTG[A/G]CTTACTCAGTTTTAC | 79658 |
| rs371613697 | snp | A/T | | | synonymous-codon, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147857603 | GAATTATAGTCTAAT[A/T]GATAAACATTTGAAT | 79658 |
| rs371614205 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147875736 | AAAAGATATTCCTAC[C/G]TGGCATCCTAACTTG | 79658 |
| rs371636376 | snp | C/T | 1.68758e-05 | 0.00290476 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148047092 | GCTGAAGGGTGGAAG[C/T]CCTGACTTTGTTCAT | 79658 |
| rs371636704 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148050015 | TGGGATTACAGGCAC[A/G]TGCCACCGCACTGGC | 79658 |
| rs371658595 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148069431 | TGGGGTTGTGGAGGC[A/G]TCTCTCTGGTTTGTT | 79658 |
| rs371674729 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147951393 | CCTTATTTAGGCTGT[G/T]GTATAGTTGATTTTT | 79658 |
| rs371686963 | in-del | -/TTGAAACTTAGTGTTATTT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148038959 | AACTTAGTGTTATTT[-/TTGAAACTTAGTGTTATTT]CTCTGTTACTTTCTT | 79658 |
| rs371693703 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148060026 | AGAGAGGGGAGAGAG[A/G]CGAGAGAGAGACGAG | 79658 |
| rs371707136 | in-del | -/T | 0.0908922 | 0.192833 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147910016 | TGGGCTTTTCTTTTC[-/T]TTTTTTTTTGATACA | 79658 |
| rs371710945 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147868384 | TGGGACTGCAGGTGC[A/G]TGCCAGCACACCCAG | 79658 |
| rs371723246 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147790786 | GATGAAATATTGTAA[A/G]CATAGTACATAGAGA | 79658 |
| rs371749572 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147897833 | CAGGTATATGCATAC[A/G]TGTGGGTGTAACTTT | 79658 |
| rs371762243 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148013333 | ATATACCTGCCTTCA[A/G]GGGATGTGTTCTTCA | 79658 |
| rs371763729 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147833999 | TGCCTCCCACGTTCT[C/G]CCTATCTTTGTCTGT | 79658 |
| rs371765347 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147991975 | CGAATTGTCAGCCAC[A/C]TTCAAAAAGTGCAGG | 79658 |
| rs371766692 | snp | C/G | 3.30006e-05 | 0.00406192 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147906605 | CCTTTTAGTGGCCAA[C/G]GGGTAACCTGATATG | 79658 |
| rs371768727 | snp | A/G | 4.95642e-05 | 0.00497792 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147822692 | GCTTTGACATAAAAC[A/G]AGAACCCAAGTCATC | 79658 |
| rs371787992 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147847554 | GCGCACCTCAGTTTT[A/C]TGGAGGAGTGTAGCA | 79658 |
| rs371794133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147746458 | CAGGCTGGAATGCAG[C/T]GGCGCGATCTTGGCT | 79658 |
| rs371799366 | snp | C/T | 3.29598e-05 | 0.00405941 | synonymous-codon, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147906671 | CATGCAGGCATTTTC[C/T]GAAGAGGAAAGGAAG | 79658 |
| rs371812943 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147780861 | GTCCACCTAGGGTGG[A/G]CTGGGCCAAGGGAAG | 79658 |
| rs371816052 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147858430 | AGTATTATCAAAATG[A/G]CACAGTATTAAGTCT | 79658 |
| rs371821694 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147878412 | TACTTCATTTTTAAA[A/G]GCTAGCTTTCAATCA | 79658 |
| rs371824208 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147916058 | GGCTACAGTGAGCTT[A/G]GAAAACAGGTAAAGA | 79658 |
| rs371839161 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147936397 | GCAGTGGCGCAATCT[C/T]GGCTCACTGCAAGCT | 79658 |
| rs371840512 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147787684 | CTTCCCTGGCTCAGC[C/G]CTCACAACCAATTCC | 79658 |
| rs371840949 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147973057 | ACCGTGACTGGCCTA[A/G]TGGTGACATTTCTGT | 79658 |
| rs371849426 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148001908 | AATACCCTTTATTTC[C/T]TTCTCCTGCCTGATT | 79658 |
| rs371865554 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148019316 | TATTATGAATACAAA[G/T]AGCTACTATTTATTT | 79658 |
| rs371868547 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147900972 | ATCCAATATACTTTG[C/T]AAAGTTTTCTGTTCT | 79658 |
| rs371871096 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148049954 | CTCACTGCAACCTCC[A/G]CTTCCTGGGTTCAAG | 79658 |
| rs371886790 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147893179 | TTCTCCTGCCTCAGC[C/T]TCCTGAGTAGCTGGG | 79658 |
| rs371898169 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147944355 | GTTGTAGTTTATTGC[A/G]TATTGCTGTCAGTTG | 79658 |
| rs371902404 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148063468 | CAGGGCCGTGCCTCA[C/G]CCAGTTCAGTAGCAA | 79658 |
| rs371917201 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147794606 | AGATTTTTTGGGATT[A/G]GTTTTTGTGTTTTCT | 79658 |
| rs371917973 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147982653 | CAGTCCTCCTGCCTT[A/G]GTGTCCCAAAGTGTT | 79658 |
| rs371954052 | snp | A/T | 0.0505692 | 0.150756 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148001696 | AATGGGAGTTCACTC[A/T]TGATTTGGCTCTCTG | 79658 |
| rs371966483 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147775914 | GACCCTTCCCACAAC[A/G]ACATCTCCGTTTTAC | 79658 |
| rs371998598 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147751883 | TTCTGAAGCCTTTAG[-/T]TTTTTTTTTTTTTTT | 79658 |
| rs372012971 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147836654 | GTGGGTTCCTTAAAT[C/T]TAAGTACCAAGTAAG | 79658 |
| rs372015372 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147862512 | CCATGGAGTGCGCAG[A/C]CCTGGCTGCACTTTG | 79658 |
| rs372021304 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147868863 | TCAGGCTCACCTGCC[A/G]CTCACCTCCTGCCAT | 79658 |
| rs372030564 | snp | C/T | 0.000153988 | 0.00877328 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147732294 | ACCGCGCAGCGACCG[C/T]TGCCGTCATGGGGCT | 79658 |
| rs372040152 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148067446 | AAGACAGACTGGCAG[A/G]TCATCTGACCACGGC | 79658 |
| rs372043748 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147977633 | TGGAGTTGAAATCTC[A/G]GCTCCACTCAATTGT | 79658 |
| rs372070060 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148050465 | TGCAAGCTCCGCCTC[C/T]TGGGTTCACGCTATT | 79658 |
| rs372077314 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147793320 | CATATATATATATAT[A/T]TTTTTTTTTTTTTAC | 79658 |
| rs372078742 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148010297 | GTTAAGTTACTCTTT[C/G]AAGACCACAGTGCAT | 79658 |
| rs372082047 | in-del | -/A | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148033420 | TGGAATTTTCAAAAA[-/A]TATTCTCACTTTTAA | 79658 |
| rs372084517 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148043508 | TCCCAGCCAGGGGTG[A/G]TGGCTCATACTTGTA | 79658 |
| rs372088597 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148062363 | CGGGGTATCTTAGGT[A/G]AAGAGCACCTGGGTG | 79658 |
| rs372091802 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148035302 | AGTTTATGGCAATTT[C/G]ATTACATCTTTTCAT | 79658 |
| rs372096246 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147963065 | AAAATATCAGGCATA[A/C]CTTCCCCAAATATAA | 79658 |
| rs372096510 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148001926 | CTCCTGCCTGATTGC[C/T]CTGGCCAGAACTTCC | 79658 |
| rs372101541 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147999632 | ACTAGTCACTGGGTT[A/C/T]CACGGTTCTCTTCAG | 79658 |
| rs372108002 | snp | C/G | | | downstream-variant-500B | ARHGAP10 | GRCh38.p7 | 4:148073270 | TTCACCCTTGACCCT[C/G]CCCTGCCCCGTGATG | 79658 |
| rs372114166 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148045363 | TAATTATTTTGTACA[A/G]TCAGTTTTCAAGATT | 79658 |
| rs372125654 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147907904 | CTGCAGTGCAGTGGC[A/G]TGACCTTGGCTCACT | 79658 |
| rs372136286 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147920181 | CAGCACTTTGGGAGG[C/T]CGAGGTGGGTGGATC | 79658 |
| rs372136466 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147983577 | GAAATTCTTTCTTTT[G/T]CATGGTCTCATCTGC | 79658 |
| rs372138021 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147837675 | TTTAAAGCAGTAGCT[C/T]TTGAATCCAAGTCTT | 79658 |
| rs372152558 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148054578 | GAGAACCTTTCTAGC[C/T]TTGGAGAAGCTCTAG | 79658 |
| rs372199389 | snp | A/G | 0.000280281 | 0.0118348 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148023270 | GTTGGAAGATTTTTC[A/G]GACGCCGCCCGATAC | 79658 |
| rs372199512 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147880253 | GCTTACTGGGTGAAT[A/G]GGTATGGTTTTGCTT | 79658 |
| rs372201510 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147935771 | AAGAAATAGAAAATC[A/G]AACAAGACTTGAGTG | 79658 |
| rs372220618 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147798257 | GCCCAAAATATCGGT[A/C]CCTGCCTCTGAACCA | 79658 |
| rs372229832 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147883377 | TAAATTTCAAGCCAG[G/T]AAGAACTCTTCCAAA | 79658 |
| rs372240163 | snp | A/G | 3.29696e-05 | 0.00406001 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148023356 | CAGTCGAAGAGACAA[A/G]GCCAGAGAACCAAGA | 79658 |
| rs372243336 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148056538 | AGACCCTTCACTTCC[C/T]CTCTTCACTTCCCGC | 79658 |
| rs372272237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148034132 | TAAACCAGCCAATAT[A/G]TGGTAAATATTGAAT | 79658 |
| rs372276820 | snp | A/T | 9.68078e-05 | 0.00695662 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147857545 | CATAGTTTTTTTTTT[A/T]TTTGTAGGAAGAAAA | 79658 |
| rs372281069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147984464 | GCTAATGCCATGCCC[A/G]TGTTTCCTTTGACCC | 79658 |
| rs372285261 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148055427 | GGCGCGGTGGCATAC[A/G]CCTGTAATCCCAGCA | 79658 |
| rs372303938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148034478 | CCCTGCCACCACTCC[C/T]GGCTAATTTTTTTTT | 79658 |
| rs372341198 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148021269 | CCACACCTCACCCCC[C/G]ACACCCTTTCCCCAA | 79658 |
| rs372366928 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147879420 | TAATGGTTTATATTT[C/T]AATGGTTTATATTCA | 79658 |
| rs372366979 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147924449 | AGAAAATTAATAGGA[C/G]TTTATTCTATCCTTA | 79658 |
| rs372408519 | snp | C/T | 8.3316e-05 | 0.00645376 | synonymous-codon, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147965028 | TTTTTTGGAAGAAAG[C/T]GGCAGCCCAGAATCT | 79658 |
| rs372409435 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147853740 | TGCTTGATTATTATG[A/G]TTTTTTTTTTATATT | 79658 |
| rs372411422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147809366 | ACATGCATTTTTTTT[C/T]TTGATCTTAAATTAG | 79658 |
| rs372417270 | snp | G/T | 9.96429e-05 | 0.00705773 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147879351 | CTTGTAAGTATTTGA[G/T]TCAACATAGAATAGA | 79658 |
| rs372427174 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147761123 | CCAGGCTCAAGCAAT[C/T]CTCCTGCCTCAGCCT | 79658 |
| rs372441825 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147843805 | AGGCGTGAGCCACTG[C/T]ACCCGGCCTGAACCC | 79658 |
| rs372454592 | snp | A/G | 0.000181847 | 0.00953364 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147955266 | TAAAAAAACTCAGAA[A/G]TGACTTGTTTGGATT | 79658 |
| rs372461135 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147763066 | AACAGAAAACCCATA[A/G]TAAAACTGTATAAGA | 79658 |
| rs372462778 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147808816 | TAGCTGCCTTTTCTC[C/T]CTCTGCCCCCTCCCT | 79658 |
| rs372470354 | in-del | -/AG | 0.0111196 | 0.0737302 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147986627 | CTAGGATCTTCAGAC[-/AG]TGTCAGGCCTCTCTG | 79658 |
| rs372474632 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147770266 | GGTCAGGTGCCAGTG[A/G]TTCACGCCTGTCTGT | 79658 |
| rs372487365 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147819805 | CTTAGGTGATCCGCC[C/T]GTCTCGGCCTCCCAG | 79658 |
| rs372500442 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147781560 | CATTTTTAAAAAAGG[G/T]TATAGTAGTCCTTAT | 79658 |
| rs372533407 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147985255 | TGGGGAAGAGAGGGC[C/T]TCACTGTACCACGGT | 79658 |
| rs372551006 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147989643 | TCTGCCCAGCTCACC[A/G]GCGGTCAGAGTTTAA | 79658 |
| rs372559867 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148019769 | GACTCCACCTAAAAA[A/C]AAAAAAACAAAACAA | 79658 |
| rs372562767 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147863207 | AGGGCTTTTTAAAAA[A/G]TCTTCCCAGACTGCA | 79658 |
| rs372576984 | snp | C/T | 1.65307e-05 | 0.0028749 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148023399 | TCTACAATCTTTGTC[C/T]GGAGCTGGAAGATGG | 79658 |
| rs372581553 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147920276 | ACAAAAATTAGCTGG[G/T]CATGGTGGCGGGTGC | 79658 |
| rs372589776 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147792606 | TATATGCTACCTGAG[C/G]TTTATTATTCCTTAT | 79658 |
| rs372594480 | in-del | -/ACTG | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147739810 | GCATGATCTTGGTTC[-/ACTG]CAACCTCCGCCTCCC | 79658 |
| rs372603873 | in-del | CTAAGCC/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148003894 | GTCTTTTATCTGAGT[CTAAGCC/G]TAAGCCTAAATCAGC | 79658 |
| rs372606618 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148055997 | GGGTGAGCAAACCGT[A/G]GCCCACTGCCACCTG | 79658 |
| rs372615012 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147939410 | ATGGTTTTCAGAAAT[C/T]ATCCAAACAATGATT | 79658 |
| rs372625974 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147966234 | GAAGCAAGATTAGCA[C/T]ATACAGTTGGCTCTT | 79658 |
| rs372632189 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148004608 | CACGTGGCAGGAAAC[C/T]GCAGGCATCCTCTAG | 79658 |
| rs372641423 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147871249 | AGGTGTGAGCCACCA[C/T]GTCCGGCCGTGTGTG | 79658 |
| rs372654600 | in-del | -/GA | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148060028 | GAGGGGAGAGAGACG[-/GA]AGAGAGAGACGAGAG | 79658 |
| rs372669343 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147962843 | AATTTTTGTATTTTT[A/T]GTAGAGATGGTCTCA | 79658 |
| rs372675564 | in-del | -/AC | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147741697 | TCTTTATAAACACAT[-/AC]ACACACACACAGAGA | 79658 |
| rs372676948 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148000077 | GCTGTCCCTCCCCCT[C/T]TCCCCACCCCATGAC | 79658 |
| rs372678180 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147910378 | TGTACAAAATACTTT[A/C]TCTACATTTACTTTA | 79658 |
| rs372708860 | in-del | -/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147970449 | GAGGGTGCAAAAAAG[-/G]AAGGTTAAACTGGGG | 79658 |
| rs372711211 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147894837 | ATCACTTGACTGTGC[A/C]TCTGTAGGTCTATTT | 79658 |
| rs372714834 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147829277 | CAGGTTGGTCTCGAT[C/T]TCCTGACCTTGTGAT | 79658 |
| rs372719228 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148069627 | GAGAAATAGTGAGCA[C/T]GTGCAGGTGAGACTA | 79658 |
| rs372739582 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147740273 | ATGTTGGCCAGGCTG[A/G]TCCTGAACTCCTGAC | 79658 |
| rs372742572 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148020243 | AAGGTTCAAGGAATT[G/T]ATTATATATGTACAG | 79658 |
| rs372761413 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147850056 | TTGTAAATGCACCAA[C/T]CAGCACTCTGTAAAA | 79658 |
| rs372770047 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148033359 | AAAGATTTGTCCATA[A/G]AAATAATGTACAGTA | 79658 |
| rs372776958 | snp | A/C | | | downstream-variant-500B | ARHGAP10 | GRCh38.p7 | 4:148073146 | CACCCCTCTCCTACA[A/C]CACCCAGCATGCCTC | 79658 |
| rs372784567 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148013811 | GTTAATTCTAAATGT[A/G]TTTACTTATACTCAG | 79658 |
| rs372802441 | snp | C/T | 4.95176e-05 | 0.00497558 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147955385 | AGCCAGTAAGTATTA[C/T]GTAAAGGTATATAGG | 79658 |
| rs372810702 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148052002 | TGCTTTTCAGGAAGT[C/T]AATAAATTTTGCTGG | 79658 |
| rs372837582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147955812 | ATAGACAGATACTCG[A/G]ATCTAAATTACAGAC | 79658 |
| rs372840937 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148002498 | GAATGGTACCAGCTC[C/T]TCCTTGTACCTCTGG | 79658 |
| rs372860881 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147978660 | GAGGCCTCCCAGCCA[C/T]GCTTCATGTACAGCC | 79658 |
| rs372889681 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148030191 | AATAAGTTCATGGCA[G/T]GTAACTCAGATTTAT | 79658 |
| rs372945850 | snp | A/G | | | intron-variant, downstream-variant-500B | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147782712 | AACTTGTTCTGAGGG[A/G]TCAGACCAGTTTGCA | 79658 |
| rs372967090 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147965813 | AAAATAGTCTAAGTC[C/T]CAGCTTTCATGAAGC | 79658 |
| rs372976141 | in-del | -/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148019777 | CTAAAAAAAAAAAAA[-/C]AAAACAAAAAACAAA | 79658 |
| rs372983933 | snp | A/T | 0.000297512 | 0.0121929 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147946739 | AAGAAAGAAGAATGG[A/T]CTATTTGGATCTGTA | 79658 |
| rs372989586 | snp | G/T | 0.000333773 | 0.0129141 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147879376 | AATAGATTATAATCT[G/T]TCAGAGGTAGTGTTT | 79658 |
| rs373006543 | in-del | -/AT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147825834 | CTGAACATTGAGCGC[-/AT]ATACCTATTGATCTC | 79658 |
| rs373010949 | in-del | -/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147811590 | TGCAATGGCTTTTTT[-/T]AAAAAAAAAAAACAA | 79658 |
| rs373012977 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147785778 | ATTATTTCATATAAG[G/T]AAGATTGTACTCTGA | 79658 |
| rs373013684 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147898190 | GCTGCCTTAGGCTGC[A/G]TTTCTTGTAATGCAG | 79658 |
| rs373068582 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148052095 | GTGAATGATTTGCCT[A/G]AAGTTCAGAAAAATA | 79658 |
| rs373092719 | in-del | -/A | 0.000835651 | 0.0204237 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147857678 | TTTATTTTTCTGTTA[-/A]CGTTTTCAAAATTTG | 79658 |
| rs373098403 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147887886 | AAAAATTTTTTTTTT[A/C]CTATTTCTTCCCTCT | 79658 |
| rs373100371 | in-del | -/AG | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148034341 | TTATTTTTTTGAGAC[-/AG]CATTTCGCTCTTGTT | 79658 |
| rs373113869 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147826997 | TTCTTCTCCCCATCC[A/G]CTTTTTTTCTCCTTT | 79658 |
| rs373114281 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147788084 | CCACAAACCAAACAC[A/C]CCCCTGCCGTTCCAC | 79658 |
| rs373122396 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147759676 | CAACGTGTAACCAGC[A/G]TAAAAATGATTGAGA | 79658 |
| rs373136690 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147862751 | ACTAAAAGATAAAAT[C/G]AAATTGATAAATCTG | 79658 |
| rs373156004 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147744782 | AAGGTATTTCGTAGT[A/C]GCCAGGAGACATGTT | 79658 |
| rs373156378 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147810682 | TACAGTGATTTGCCT[C/T]CACATCAAAGACCTC | 79658 |
| rs373158786 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147801713 | TGGCACCACCCAAGC[A/G]AATTAATCTCATAGC | 79658 |
| rs373159542 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147895385 | TGTGACAAAAACAGC[C/T]TTAGGGCCAGGCATG | 79658 |
| rs373173491 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147798254 | GCAGCCCAAAATATC[A/G]GTACCTGCCTCTGAA | 79658 |
| rs373177839 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147771940 | GGGACAACAGGCGTG[C/T]GCCACCACGCCCAGC | 79658 |
| rs373184867 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147754869 | GAGGTGGAGGCGGCT[C/G]GATCACCTGAGGTCA | 79658 |
| rs373185356 | in-del | -/TTTG | 0.000865485 | 0.0207844 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148046858 | TTTCTTCTCCAGGTA[-/TTTG]TTTGATATTCAATGC | 79658 |
| rs373186007 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147909182 | TTTAGTAGTACATTA[A/T]AAAAGTTACAACTCT | 79658 |
| rs373197675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147835659 | GATTACAGGCATGAG[C/T]CACTGCGCCTGGCCT | 79658 |
| rs373220393 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147941135 | TCTTTCATTTCCAAG[A/T]TGGTGTTATGATGAT | 79658 |
| rs373225572 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147739821 | GTTCACTGCAACCTC[A/C]GCCTCCCAGGTTCAA | 79658 |
| rs373233129 | in-del | -/AGTGTTAAGCTA | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147833708 | TATATAAAAGTGCTA[-/AGTGTTAAGCTA]TTATTTCAAGATTAG | 79658 |
| rs373233339 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147763877 | CTTGTGCCTCAGCCT[C/T]CTGAGTAGCTGGGAT | 79658 |
| rs373233643 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147853545 | ATAGAAAAATGGGCA[A/G]TTCACAATTATGTTT | 79658 |
| rs373236657 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147891384 | ATTCCATTTATATGA[A/G]ATGTGCAGGACAGAC | 79658 |
| rs373275914 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147782366 | TTCCACATGGCATAT[A/G]CGTTTTATTATCAGC | 79658 |
| rs373287966 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147857420 | CAGATATGTTTTTTT[-/T]AGATAGCTTTATCAC | 79658 |
| rs373307853 | in-del | -/AATA | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147935028 | GGCACATATCTGATG[-/AATA]AATATATGACAGTTG | 79658 |
| rs373311495 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147888231 | CCTTGTCCAGTCTTA[C/T]GACTTTATGTGCCAT | 79658 |
| rs373327910 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147845501 | ACTTTGGAGAAGCAC[A/C]TCTTTGGTACTTTTA | 79658 |
| rs373348127 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147806856 | ACAAGTGTATGCCAT[C/T]CTGCCCAGCTAAAGG | 79658 |
| rs373355998 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147788636 | GCTCCTTTTTACACA[A/T]TTGCGGTATTTGGTG | 79658 |
| rs373357791 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148013063 | TTTATCAATTAAAGC[A/C]AAGTGTTCCTATAAA | 79658 |
| rs373369623 | snp | C/T | 0.000185452 | 0.00962765 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148023462 | ATGTTGAGAGTATGG[C/T]GTATCATATGTCGTC | 79658 |
| rs373373165 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148005194 | TCCCAGTGTCTATAA[C/T]GCTGCATGTCCCATA | 79658 |
| rs373374081 | in-del | -/AT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148043614 | GAGACCCTCTCTCTA[-/AT]ATATATATATATATA | 79658 |
| rs373381476 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148056537 | TAGACCCTTCACTTC[C/T]CCTCTTCACTTCCCG | 79658 |
| rs373388769 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147974893 | CTCCCCTTTATAAAA[C/T]CATCAGATCTCATGA | 79658 |
| rs373398935 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147951601 | ATTTTTTTCTTTTAT[C/T]TTTCAATTTTCTTTT | 79658 |
| rs373408868 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148057206 | CAGCCAACAATGATA[A/G]TGCCAGCTCTGGCAC | 79658 |
| rs373409656 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147877234 | GGCAGTTTTTTTTTT[-/T]CTTAGAGTTAAATAA | 79658 |
| rs373411696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147913218 | AAAATACTTCTTGCT[C/T]TTAAGTGTTACAGAA | 79658 |
| rs373416821 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147918646 | CTTCATCTCCCTAGC[C/T]GTCCAGCCTACCTGG | 79658 |
| rs373418122 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147942377 | GAATTTTTTATTGCC[A/G]TTTTTACACAAAGTA | 79658 |
| rs373422094 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147801002 | GTAGAGACAGCGTTT[C/T]GCCATGTTGGCCAGG | 79658 |
| rs373428584 | snp | A/G | 3.29794e-05 | 0.00406061 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147913103 | AAGATGGGGTTCACA[A/G]TTATCAGAAAATGCA | 79658 |
| rs373433317 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147764634 | CGCCTCTTGGGTTCA[A/G]GGGATTCTCGTGCCT | 79658 |
| rs373450381 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147792105 | TCTTCACCTTTACTC[C/G/T]ATAGTACACATTGCT | 79658 |
| rs373451901 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148069514 | TCCTTTCACCTCCAG[C/T]GTTGTAGAAAATCAC | 79658 |
| rs373461349 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147960462 | CGATGGTAAGGTGTT[C/T]CATTTAATGACACTG | 79658 |
| rs373469696 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147768651 | AAATGGATGGTAGAA[A/G]TTGTAGAAGCTGAAT | 79658 |
| rs373473461 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148021305 | TCACTTCAAACTGGA[A/G]GAAAGAGGTGGGGCA | 79658 |
| rs373495183 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147815275 | CTGTGTCCTCTTCTG[C/T]TGTAGTGATAGTTAA | 79658 |
| rs373501853 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147736507 | AATGGGACTGATACA[G/T]AAAGCCTTGAGGAAT | 79658 |
| rs373507356 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147912410 | GCTGGGCTTGGTGGC[A/G]GGCACCTGTAATGGC | 79658 |
| rs373510704 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147776367 | TGGAATTACAGGAAC[A/G]CGTCACCACACCCAG | 79658 |
| rs373514100 | snp | A/C/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147945818 | AAAAATTAGACATGC[A/C/G]GACACAGTGAAGGGT | 79658 |
| rs373521537 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147898322 | TTATACATCTTAAAG[A/C]AGTCATTTCATTGTC | 79658 |
| rs373523883 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147768891 | TTACAGGCACACACT[A/G]CTATACCTGGCTAAT | 79658 |
| rs373525936 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147931694 | ATCTGAAAATTCCAA[G/T]GCTAGGTGTGTTTTG | 79658 |
| rs373537663 | in-del | -/GT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147899309 | ATGAAAGCAGCTGGG[-/GT]GTGTGTGTGTGTGCA | 79658 |
| rs373546954 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147885701 | CTTCCATGACAGTTA[A/G]CCATTCTGGTTCTCC | 79658 |
| rs373566419 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148070521 | TCTTCCAAACTGTGG[A/G]CAGCTATACCTTAGA | 79658 |
| rs373578495 | snp | A/G | 3.31033e-05 | 0.00406823 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147881967 | GGACATGGTGAAAGA[A/G]TCGTTTTAAAAAAAT | 79658 |
| rs373590665 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147872481 | TGTTTATATAAACAC[G/T]TGTGCTCTGTGTATA | 79658 |
| rs373591713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147793202 | TGTGTGTGTGTGTGT[A/G]TATGTGTGTATATAT | 79658 |
| rs373613522 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147778124 | TCCTGCTAGAAGTGT[C/T]GGTTTAGCGCTGAGA | 79658 |
| rs373615477 | in-del | -/T | 0.413914 | 0.188765 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147898180 | GTTCCTTAGGCTGCC[-/T]TTAGGCTGCATTTCT | 79658 |
| rs373669059 | snp | G/T | 0.000153988 | 0.00877328 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147965141 | CAAAGTAAGCCTCTT[G/T]TTCTTCGTTTTAACT | 79658 |
| rs373691154 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147756320 | GTGTGGGTGGTGGGG[A/G]GAGTATAAAATATTG | 79658 |
| rs373695727 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147806997 | GGTGAAAGGATGCTA[C/T]GCCTAATTCATATGT | 79658 |
| rs373700761 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147765779 | CACTCCAGCCTGGGC[A/G]ACACGATGAGACCCT | 79658 |
| rs373710174 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147769117 | TTCATTATTGCTCTC[A/C]GGAACTGGATAATGC | 79658 |
| rs373713688 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147765346 | GTGTGTGGGGGGGGG[-/T]GGTGTGAGTGTGTGT | 79658 |
| rs373738736 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147762208 | AGATCTGGTTTCACC[A/G]TGTTGGCTGGGCTTG | 79658 |
| rs373746158 | in-del | -/TG | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147933426 | TTGTGACAGTGTCTG[-/TG]CATTGAGGGATTAGC | 79658 |
| rs373750239 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147816769 | CTGCTGGTTTTGTAA[A/G]ACAGGAAAACGTGAA | 79658 |
| rs373764532 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147928503 | TGCGTTTACACAAAG[A/C]GTAGGAGAAGGCGAA | 79658 |
| rs373768423 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147904630 | TTAATCCAGTCTATC[A/G]TTGTTGGACATTTGG | 79658 |
| rs373774332 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147976817 | AGAGTCATTCTGCAT[A/C]ATTTTAGTGCCCAGT | 79658 |
| rs373793541 | in-del | -/CCCATGATCCAATTACCTCCACC | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147824747 | ATGGGGGAAGCCACC[-/CCCATGATCCAATTACCTCCACC]TGGTCCTGCCCTTGA | 79658 |
| rs373796952 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147917341 | TGGGTTTTTCAAGAT[A/G]CGATAAACAGACAAC | 79658 |
| rs373817908 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147902602 | AAAAATTAGCTGGGT[G/T]TAGTGGCTGTGCACC | 79658 |
| rs373825930 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147734587 | TTCCTATCAAAGACT[A/G]AGAGCCTTGGACTAA | 79658 |
| rs373828246 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147874256 | GGTATTAATACAATT[A/G]TTTTTGAGCCTGGAT | 79658 |
| rs373829021 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147762906 | CATCAGAACATCTGT[C/T]GCCCTTATCTACTCT | 79658 |
| rs373842188 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147829591 | TCTGATACAGTTAGT[G/T]GCTGCAACTGCTCTA | 79658 |
| rs373853100 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148034357 | CATTTCGCTCTTGTT[A/G]CCCAGGCTAGAGTGC | 79658 |
| rs373859702 | snp | A/G | 0.00242952 | 0.0347686 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147909800 | CTCATTTATAAAAAT[A/G]ATTGTATCCTCCTTT | 79658 |
| rs373859881 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147737714 | TACAGTGGCTGGTCT[A/C]CAGTGTGAATGTAGA | 79658 |
| rs373862001 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147818758 | AACTGCCTTATGCTT[C/T]TGTTTTGAAAAGAAG | 79658 |
| rs373867409 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147823556 | CAAGCTCAGGAGTTC[A/G]AGACCAGCCTGGCCC | 79658 |
| rs373890254 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147886682 | GAGAAGCAATTTCTA[C/T]TGTATTCATGGGATC | 79658 |
| rs373898600 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147870788 | TAGAATTCTTCCTGG[A/T]AGGAAATACAGTGTG | 79658 |
| rs373907010 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147866503 | CTAATGGCTGTGATA[-/T]TTTAAGGGAAAAAAG | 79658 |
| rs373908705 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147957565 | GCTGACTGCTAAAAT[C/T]ACTAAGCATCAGCAG | 79658 |
| rs373910597 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147793323 | ATATATATATATATT[A/T]TTTTTTTTTTACAAA | 79658 |
| rs373913531 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148017271 | GAAATGGAGGTCTTA[C/T]GACCTAAAGTCAGAC | 79658 |
| rs373929197 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148062187 | TTGCTGAGTGTCACC[A/G]TGTTGGAGGATTGCA | 79658 |
| rs373945284 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148051389 | AACAGGTTTTCTTCT[A/G]TTGTAATTGATGGAG | 79658 |
| rs373959232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148009442 | TGGCCGAGATCCTCA[A/G]TAATTTATAAGAGTA | 79658 |
| rs373965753 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147933734 | GGCCCAGATGGATGT[A/G]TCTCCCAGCAGGTCT | 79658 |
| rs373966182 | in-del | -/AG | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147956494 | AGGATTTTTTAAAAA[-/AG]AGAATTTGTGAGATC | 79658 |
| rs373967971 | snp | A/G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147980857 | CATAGTAGTCTCTGG[A/G/T]GATCTTTTCTATTTC | 79658 |
| rs373977013 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148025004 | CGTTTTGGTCTTAGG[A/T]TCACGTCTACTATTT | 79658 |
| rs373994140 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147994112 | CACAGTTAGAAAGTT[C/G]CTTGTGGTCTTTCTA | 79658 |
| rs374000912 | snp | C/T | 1.67301e-05 | 0.00289219 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147864818 | TTCACCATCTCCAGT[C/T]TGACTAACCTCTGTG | 79658 |
| rs374001381 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147934985 | AATTTTACTCACTGT[C/T]GAATCTTGGGCAACC | 79658 |
| rs374002657 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148032363 | TATTGTAGGCCAAAC[A/G]TTGTAATCATTGAGA | 79658 |
| rs374007664 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147899857 | AATAAAATGTAGGGC[A/C]GAACTTGTTACGTGC | 79658 |
| rs374008037 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147795327 | TGTTTACTTTTTTAC[A/C]TTTTATCCTACGTTT | 79658 |
| rs374019974 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148016510 | CCTTGTCTCTGAAAG[A/C]AAAAAAAAATTGAGG | 79658 |
| rs374020706 | snp | A/G | 3.29495e-05 | 0.00405877 | synonymous-codon, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148046956 | CTCACTTTCCTCCCC[A/G]TCTCCCGTGACTACA | 79658 |
| rs374021414 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148048518 | TTTACTCTTCCTTTT[A/C]CACAATAAAAATTCT | 79658 |
| rs374029769 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147918329 | TTTAGTAGAGACAGG[G/T]TTTCACCGTGTTAGC | 79658 |
| rs374031511 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147870215 | GTCCCACCTGCCACC[A/G]TGCCCGGCTAATTTT | 79658 |
| rs374036499 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147929523 | TAGAAAGTGCTTACT[A/G]TACTTAAACAGACAT | 79658 |
| rs374048082 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148034329 | GGCAATTACTTATTT[A/T]TTTTTTTGAGACCAT | 79658 |
| rs374056142 | in-del | -/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147838484 | CTCTTAAAAAAAAAA[-/C]ACACACACACACACA | 79658 |
| rs374067869 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148072672 | GGCAGCGTGCACTGG[C/T]GTATTTGTAACAGGC | 79658 |
| rs374068556 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147855214 | AGAGAATGTTTGTGA[A/C]CTTGCTACAGAGTCA | 79658 |
| rs374074720 | in-del | -/G | 0.00636936 | 0.0560724 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147787917 | GAAAGTGAATAAGGA[-/G]GGTACCTTTGATAGG | 79658 |
| rs374080263 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147789468 | CTAATTTTTTTGTAT[C/T]TTTAGTAGAGATAGG | 79658 |
| rs374087781 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147866925 | GCTGATCTGTTTGTA[C/G]TGAGAAACTGAGGGT | 79658 |
| rs374128534 | in-del | -/TCTATCTG/TCTG | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147839142 | CTATCTATCTATCTA[-/TCTATCTG/TCTG]TCTGTCTGTCTGTCT | 79658 |
| rs374135565 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148060345 | GAAGCTCATGTTTAG[-/T]TTTTTTTTTTTTTTT | 79658 |
| rs374144625 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148053050 | CCACCAGACTTTGTT[G/T]CAGCTATTTTGTAGA | 79658 |
| rs374150548 | snp | C/T | 0.00285073 | 0.0376462 | synonymous-codon, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147875122 | AAGTCAGTTTACAGC[C/T]GAAGGCTACCTGTAT | 79658 |
| rs374166652 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148036308 | AAGAAAATTATCTCA[C/T]TCAGTTCCTTAGCCA | 79658 |
| rs374179210 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148017865 | GTATTTCTGGCAGAA[A/G]TGGTGTAGTCATTTC | 79658 |
| rs374180600 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148042297 | TTTTGAAGCTGTTCT[A/C]CAGATCGTATCACTT | 79658 |
| rs374184768 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147916399 | AGCTATCTATTCAGT[A/C]TGTGTATGACTTATG | 79658 |
| rs374185126 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148062310 | CAGAAGCCTCGGGAA[A/G]CTGCTCGTGGAAACT | 79658 |
| rs374198749 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147943110 | AATAGTTCATGGTAG[A/G]TTAGAACTGATACGA | 79658 |
| rs374199958 | snp | A/T | 1.65888e-05 | 0.00287996 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147881797 | AGTGTGTATATACTT[A/T]TCCTGTAGGTTTTGA | 79658 |
| rs374201810 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147993576 | GAAAGTCAGCTGTGC[A/C]ACTGTGACACAGTAG | 79658 |
| rs374207223 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147998160 | AGAGAAAAAAAGTAG[C/T]GTTTATGAATCCTAA | 79658 |
| rs374207710 | snp | A/G/T | 1.65241e-05 | 0.00287433 | synonymous-codon, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148072057 | GAGGGGGCTGATTCC[A/G/T]CAGAACTACGTCAAG | 79658 |
| rs374225540 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148035673 | ACTGAGAATTGGACT[A/C]AGTGGAATTTTAGGA | 79658 |
| rs374320622 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147949849 | ATTGCATTCTTTTTT[C/T]CTCCATTCCGTATGG | 79658 |
| rs374343855 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148032883 | TGGGAGAAAGATGAC[A/G]GCTGTGGAAGATTCA | 79658 |
| rs374344355 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147926939 | AGGTGTTATTTTCTC[A/C]TAAGAACCATGTGAG | 79658 |
| rs374369181 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147900287 | ATGAATGAATGAAAG[A/T]GGTTGAGATGCTGAT | 79658 |
| rs374371724 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147935529 | AAGTCAAAGATTTCA[A/G]ATTTCTAATACTTGT | 79658 |
| rs374380556 | snp | A/T | 0.000496065 | 0.0157412 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147906593 | AGGAAAAACTTGCCT[A/T]TTAGTGGCCAAGGGG | 79658 |
| rs374381787 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147922965 | ATCCTTTGCTTGCCT[C/T]TTCTCATTTCTAAAT | 79658 |
| rs374412771 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148052523 | AGGAATGAACTTCCC[A/G]TTGCAAAAACTTCCT | 79658 |
| rs374425788 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147861862 | GCTGATTGGCCCATG[C/T]GCAGCCATGAGTGGG | 79658 |
| rs374430893 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148031112 | TTTTGGATCTACTAA[C/T]AGTCTTTAAAATCAG | 79658 |
| rs374432629 | in-del | -/CTTTA | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147943160 | CTTCCTTCTTCCCTA[-/CTTTA]GTTTAAAACATCAGA | 79658 |
| rs374432666 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147822275 | GCAATTGGTTAAGAG[A/C]AGCTGGTTGGCTGAC | 79658 |
| rs374445465 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147854310 | ATCAGAAGACATGGC[C/G]AACATACTGGGCTTG | 79658 |
| rs374460007 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147992840 | ATGAGCTTGTACCAC[A/G]GGACTTTCTACTTAA | 79658 |
| rs374462731 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147975944 | TGCCACGATCAGTAG[A/G]ATGCATTGGTGCTCC | 79658 |
| rs374478419 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147760507 | CTGGGTGGGAAGGTA[C/G]AAGGGGAGGGGCCAT | 79658 |
| rs374486541 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147882857 | ATCCTAGTGTTCATA[G/T]AATATTTGCTTTTTA | 79658 |
| rs374490015 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147779208 | CCACTGCTGTGGGGA[A/G]CATGTAAGCTGCGGC | 79658 |
| rs374491026 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148059204 | GTGTAGTGTGTTAAG[C/T]TGGGAAGATAGCGAA | 79658 |
| rs374513583 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147759834 | GCTCACCACAACCCT[C/T]GCCTTCCAGGCTCAA | 79658 |
| rs374515096 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147915251 | TCTCTTACAGTGGCA[A/G]TTCACACTGGCAGGT | 79658 |
| rs374524284 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148025469 | TAAAGCAACTTAAAA[C/T]TATTATTCTCCCTTG | 79658 |
| rs374528335 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148017114 | ATGATTGATCATCAA[A/G]CAGAAATATAATTGT | 79658 |
| rs374555328 | snp | A/C | 4.94621e-05 | 0.00497279 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148063141 | TCCTTCAAACTCCTA[A/C]CCTTAGCCCAGGCCA | 79658 |
| rs374560221 | in-del | -/GATT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147890296 | AGCCATTACTACTTT[-/GATT]ATCAATGGTTAGATG | 79658 |
| rs374575633 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147838646 | TCAACTAGCCTCCCA[C/G]CTCAGCCTCCTGGGT | 79658 |
| rs374585504 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147942582 | CACTATCCTTCTCTC[C/T]GTCCTCCTTCTCCTG | 79658 |
| rs374614012 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147998916 | TTCTATTAACTATTG[C/T]CCTGGAAGAACTAGA | 79658 |
| rs374620304 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148030004 | CAGCATCCCCCCCCC[C/T]ACCAACCCCAATGCT | 79658 |
| rs374648105 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147986087 | AGTGGCTGAGGTATG[C/T]GGAAAGCCTCTCATC | 79658 |
| rs374653930 | in-del | -/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147947227 | TTTATGAGTCACTGT[-/C]TTTTTTTTTTTTTTT | 79658 |
| rs374656641 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148040153 | TATTGCCAGCACAAT[C/G]TTCTTGTCCTTGGGA | 79658 |
| rs374666538 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147808231 | GGGGTTTCTTATGCA[A/G]GTTGTATGTGGGTTT | 79658 |
| rs374668044 | snp | A/G | 6.64982e-05 | 0.00576582 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148023425 | GATGGTAAGATGTTA[A/G]TGATATTTTTTGCTT | 79658 |
| rs374668302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147886514 | AGTCTGTTGTTCGTC[A/G]TGCACTCACTTTCTT | 79658 |
| rs374668432 | in-del | -/CT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147785715 | CATTTGATTTTCACT[-/CT]GTCATTGTTAGCTGT | 79658 |
| rs374670972 | in-del | -/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147840484 | CAGTTGGAAATGGCT[-/G]GTTTTAAAATGTGGT | 79658 |
| rs374678433 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147864282 | CAGACGTTCTGAGGG[C/T]CGCAGATGGGCGTCC | 79658 |
| rs374679440 | snp | C/T | 1.67725e-05 | 0.00289585 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148023212 | TACTGGAGTAACACA[C/T]AGGTTTCTGTTCATG | 79658 |
| rs374691054 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147984095 | CTTGGTTGCAGAGAG[A/G]TTCCTACAGTGGCTT | 79658 |
| rs374700767 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148049023 | TTATTTTTTTCTGTG[C/T]CATGGATGGAATACA | 79658 |
| rs374709295 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147906643 | TGTCTTTCAGGCCTG[A/G]CGTTTCCTTGACCAT | 79658 |
| rs374732046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147969742 | ATTTTCCAGTAGCGT[C/T]GGCAAGCCTGTTACA | 79658 |
| rs374733576 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148022075 | TGTAAGTGATATACC[C/T]TCACTTGTATCGAAG | 79658 |
| rs374739263 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147924245 | ATCCTTCCTCTGAGA[C/T]GGCGAACCCCGAGTC | 79658 |
| rs374742420 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147742526 | CTCGCTTTTGCAGCT[C/T]AGGCTGGAGTGCAAT | 79658 |
| rs374745132 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147852300 | CGAGGTGGCACTTTG[C/T]CAGCGTTGGTGCTGC | 79658 |
| rs374746167 | in-del | -/TGTG | 0.404559 | 0.196498 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147870929 | ACCAAAACTACAGAC[-/TGTG]TGTGTGTGTGTGTGT | 79658 |
| rs374752738 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148043781 | GTATATATATGTATA[A/T]ATATATGTATATATA | 79658 |
| rs374756695 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147966390 | CAGACTTTGGTGTCT[A/G]TAGGGATTCTGGCAT | 79658 |
| rs374767822 | in-del | -/A | 0.247053 | 0.249983 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148030872 | TGAAAGAAAAAAAAG[-/A]AAAAAAAAAACCATT | 79658 |
| rs374769828 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148051426 | CCTTGACAAGTAATC[C/T]TTTTAGATTCTCTGC | 79658 |
| rs374770682 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148006099 | AATTAAGGCCCTAAC[A/T]CTGGCAGCTGCCACT | 79658 |
| rs374771437 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148011372 | GTGGGCTGGAATCAT[C/T]TGGAGGCTTCTGCAC | 79658 |
| rs374783712 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148029923 | TAATTGAGTTGTGGC[A/G]TGCCTAGAAATTATG | 79658 |
| rs374793436 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911657 | GTGAGCCACCGCGCC[C/T]GGCCTCTTAACTTAA | 79658 |
| rs374794611 | snp | A/G | 9.89071e-05 | 0.00703163 | synonymous-codon, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148064470 | AGCAGAACACAGCTC[A/G]GAATTATCTTTTGAA | 79658 |
| rs374800440 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147973587 | TGTAAGAAATTATTG[A/T]TGACTTCAGTCATCC | 79658 |
| rs374834943 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147940322 | GATTCTCAGGGATTC[A/G]TTGGTATTCACAGTG | 79658 |
| rs374838764 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147946834 | GGAAAATTTATCAGG[-/T]TGTCTCAGTGTCCCA | 79658 |
| rs374851836 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147851309 | GTCCAGGCTGGGCAG[C/T]AGCCTTGAACTCCTG | 79658 |
| rs374859333 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147833691 | AAAGAGCTTTTTCAA[C/T]GTATATAAAAGTGCT | 79658 |
| rs374867040 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147814259 | GTCTTGGATCACAAA[A/G]GAGGATGTTTTAGCC | 79658 |
| rs374867408 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147794120 | GGGACAGGCTCGAAC[A/G]CAAATAATTATGGTG | 79658 |
| rs374871646 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147767420 | GGGGTTCTGAGTGGT[A/G]ACTTAGTTTCCCTGC | 79658 |
| rs374891561 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148034865 | AATAACACATGGCTG[G/T]TATATTTTTTGTTTA | 79658 |
| rs374911249 | snp | C/T | | | upstream-variant-2KB | ARHGAP10 | GRCh38.p7 | 4:147730993 | TTCAAGCGATTCTCC[C/T]GCCTCAGCTGGGACT | 79658 |
| rs374918450 | snp | C/T | 3.40925e-05 | 0.00412857 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147864972 | GTGAGTATTGCCAAG[C/T]TGTTTGCTGGTGGAT | 79658 |
| rs374919155 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147883787 | GCAACCTCTGCCTCC[C/T]GGGCTCAAGTGATTC | 79658 |
| rs374929352 | snp | A/G | 3.30224e-05 | 0.00406326 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147822696 | TGACATAAAACAAGA[A/G]CCCAAGTCATCATTA | 79658 |
| rs374932521 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148013645 | GTGAGCTGAGGTTGC[A/G]CCACTGCACTTCAAC | 79658 |
| rs374954278 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147943363 | TTGTTTCCTTTGTAG[A/G]ACAGCTTTGTTGCAT | 79658 |
| rs374973763 | in-del | -/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148026217 | GTGTGATGTCCCAAA[-/C]CAGCCAGTCTTGGAA | 79658 |
| rs375011153 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147955181 | GTATCTTTTTTGATA[C/T]GTAAAGGTATTCCCT | 79658 |
| rs375018133 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148007078 | CACTTCAAGGAGGTT[A/G]ATCATCCTATTCTTG | 79658 |
| rs375021691 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148026285 | TCAAAAAAGCATCAG[C/T]GAAGAGTCAGCAAGC | 79658 |
| rs375025852 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147784672 | TAAAATATATATTAT[A/G]TATTATAAATATAAA | 79658 |
| rs375034312 | snp | A/G | 9.90966e-05 | 0.00703836 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147879273 | GTCAAACACTATTGC[A/G]TGTATCGAAAAGCAG | 79658 |
| rs375036734 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147969190 | TTGTTGCATTGGCTG[G/T]TTGCTGGAGCAGTTC | 79658 |
| rs375059886 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147732499 | TGCGGCGTGGCGAGG[C/T]GGCTGGGGGAGCCTC | 79658 |
| rs375065316 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147922683 | ACAGAGCGAGACTCC[A/G]TCTCAAAAAAAAAAA | 79658 |
| rs375073946 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147847738 | TATATTGTGTGTTGT[A/G]TAGTACTGTGCTGGG | 79658 |
| rs375086805 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147846807 | ATTTCTAAGGAGGGG[A/G]AAGGAAAAAAACAAT | 79658 |
| rs375094244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147879618 | GTTACATAGGTATGC[A/G]TGTGTCATGGTGATT | 79658 |
| rs375096671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147770488 | TGAGATTGTGCTACT[A/G]CACTCCAGCCTGGGC | 79658 |
| rs375097702 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147893703 | TGGAAAGGGCTTTGT[A/G]TCTTGACTCTTCCAT | 79658 |
| rs375105081 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147925158 | GTAAAATAGCCAGAG[G/T]CTCAGGAAGAACACC | 79658 |
| rs375119535 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147771549 | ATACTAGGTGGCACA[A/G]TTTTTTTGTACCCAT | 79658 |
| rs375121396 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147826665 | CCTCAGACCAGTCTC[A/G]TTTCTCCTGTGATCC | 79658 |
| rs375147185 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147773537 | AACTCGATGTACACT[G/T]AAATATTGTATTCTG | 79658 |
| rs375154767 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148054165 | CTCAATATCTAAATA[A/G]AGTAAGGACCTCATG | 79658 |
| rs375164164 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148072306 | TGTCAGGATTCGCAA[A/G]ATGGACTTTTCATTT | 79658 |
| rs375166048 | in-del | -/AC | 0.350546 | 0.22889 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147741768 | GATATCGTTCTCTTT[-/AC]ACACACACACACACA | 79658 |
| rs375177850 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147793765 | AGAAACAAATCATCC[A/G]TGCCTGTGTACGTGC | 79658 |
| rs375188932 | snp | A/C/T | 0.000134802 | 0.00820886 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147965126 | TGGTGAAACACTTAA[A/C/T]AAAGTAAGCCTCTTT | 79658 |
| rs375191425 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148063088 | GGATTGGGATGTTGT[G/T]CATTTCGTGTTCTGT | 79658 |
| rs375196004 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148003432 | GATGTCTATTAGGTC[C/T]ACTTGGTGCGGAGCT | 79658 |
| rs375201445 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148027419 | ACATTTGGATCACGA[A/G]TGTGCTAACTGCAGC | 79658 |
| rs375206633 | in-del | -/GAC | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147852014 | AATGAGACTTACGAC[-/GAC]ACTTGTCTCAGGAGG | 79658 |
| rs375224792 | in-del | -/TAAAG | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147880710 | GCATTGCAAATTAAG[-/TAAAG]ATAAATTCAGGGTGA | 79658 |
| rs375228793 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147879641 | TGGTGATTTGCTGCA[A/C]CCATCAACCCATCAT | 79658 |
| rs375244008 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147834224 | CCTGTAGTCCCAGCA[A/C]TTTGGGAGGTGAGGC | 79658 |
| rs375261126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147918855 | ATCTCTGAGGACACA[C/T]GTTGTGCCTGGCATT | 79658 |
| rs375266770 | snp | A/G | 1.64882e-05 | 0.00287121 | synonymous-codon, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147966728 | TGTGGCAAACTTAGG[A/G]GTGGTGTTTGGACCA | 79658 |
| rs375269815 | in-del | -/ATTTTAT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147858174 | CAGGAAGGAATTTAT[-/ATTTTAT]TTTTCATTTTCTCTT | 79658 |
| rs375275573 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147907805 | GTCAGATTTGGGTGT[C/T]GTCTTACCATATTTG | 79658 |
| rs375280093 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147970156 | CTGCAGAGTCCAGGC[C/T]CTGCTATGAGGAAGA | 79658 |
| rs375284957 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147747003 | GGGATGGCATACAGA[C/T]GTTAAGCTGAGAAGA | 79658 |
| rs375285577 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147915501 | TTTCTGCCTGAATAG[A/G]TGCAGATCTATCTAG | 79658 |
| rs375294759 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147920987 | CTGGGTGAATACTAG[A/G]AGGTGATACGTAGCA | 79658 |
| rs375294867 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147890234 | ACTTTACTATTACTG[A/G]GAACCAATGGGAGAA | 79658 |
| rs375297949 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147891955 | GCCACTTTGTGCTGT[A/G]ACCCCCCCACACATT | 79658 |
| rs375307883 | in-del | -/TTTTTTTTT | 0.5 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148039371 | ATACTACTTCAATTT[-/TTTTTTTTT]TTTTTTTTTTTTTTT | 79658 |
| rs375340724 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147886873 | CCTCCTGGGTTCAAG[A/C]AATTCTTATGCCTTA | 79658 |
| rs375346731 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148034045 | TCTCAGCAAATCTCT[C/T]TCTAAGCCTCACAAA | 79658 |
| rs375359350 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147825371 | AGAATCAGTTGAGCC[C/T]GGGAGGCGGAGGTTG | 79658 |
| rs375384223 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148035493 | GATACATTATATTAG[C/T]CAAGTGAATTATTAT | 79658 |
| rs375392270 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147895646 | AGCCATAATCGTGTC[A/G]CTGTACTACAGCCTG | 79658 |
| rs375393104 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147958819 | TGCCTCTGTGTCTTC[A/G]ATAAGCTCCATGATC | 79658 |
| rs375397993 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147890624 | CTGAGGTCAGGAGTT[C/T]GAAACTAGCCTGGCC | 79658 |
| rs375423728 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148013901 | CCAGGAGAGGAAGTC[C/T]TCTTCTTGGGTATCC | 79658 |
| rs375427730 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147987096 | TTTTCAGAAATCTAA[A/T]ATTATACCAGATAGA | 79658 |
| rs375428490 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148054912 | TGGCCCTGTTGAAGA[A/T]GTTCAGCCTTCACAT | 79658 |
| rs375431579 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147944054 | TGGATTTTAAAAAGG[C/T]GGTTTGCTGGTAGCA | 79658 |
| rs375438562 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147962686 | ACTCCCTTTATTTTT[-/T]ATTTTTTTGAGATGG | 79658 |
| rs375450259 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147908257 | CTAGTCTTCTTTAGT[A/G]AAGACAGCACACTCA | 79658 |
| rs375453786 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147838104 | ATTTAATAAAAAATT[C/T]GTCCCAGCTCTTGGC | 79658 |
| rs375454952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148003842 | TGAATACAGCACACT[A/G]ATAGGTCTTGACTCT | 79658 |
| rs375457536 | in-del | -/TG | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147810888 | TGAGCATCTACTCTG[-/TG]CCTCATTTTGTTCTA | 79658 |
| rs375466168 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147819869 | CAGCCTATTGTATCT[G/T]ATTTACAGGTTTGGC | 79658 |
| rs375472623 | snp | A/G | 0.000115635 | 0.00760289 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147955288 | GTTTGGATTTATTTG[A/G]TAATTCTGAGCTGTT | 79658 |
| rs375472970 | in-del | -/CTGTCTAT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147839152 | TATCTATCTGTCTGT[-/CTGTCTAT]GTATATATAAAGTTT | 79658 |
| rs375476820 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147901502 | TTCTTTCCTTGTGAA[C/T]GATCCATTTCTACTT | 79658 |
| rs375490531 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147798277 | CCTCTGAACCATCTT[C/T]GTTGTCTCTGGCTGT | 79658 |
| rs375500924 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148000753 | TCTGTTCGTATCCTT[C/T]GCCCGCTTTGTGATG | 79658 |
| rs375501399 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147747575 | GAGTGTGGAGACCTT[C/T]AGATGCTTCAGAGGG | 79658 |
| rs375524610 | snp | A/T | 3.32369e-05 | 0.00407644 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147866826 | CAGAATGTAAGGAAG[A/T]GAAAGCTTTCTTTAT | 79658 |
| rs375538995 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911577 | CCGTGTTAGCCAGGA[C/T]GGTCTTGATCTCCTG | 79658 |
| rs375562654 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148004093 | TTAGAGCCAGGTCCA[A/G]TGGTGCACGCCTGTA | 79658 |
| rs375573967 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147921550 | CCATATAGCATTTGG[G/T]ATAATGACAGAGAGC | 79658 |
| rs375581208 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148021449 | ATGCTTTGGATATAC[C/T]GGCTGTGTGTATGGT | 79658 |
| rs375585812 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147878036 | CCGCCTCCTGGGTTC[A/C]AGCCATTCTTCTGCC | 79658 |
| rs375594112 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147808292 | GGAAGGCAGAGCATG[C/T]ACAAAGACTGCAAGG | 79658 |
| rs375609014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148069075 | AGCCCTGTTGTCCGC[A/G]TAGACACTGCTTGGG | 79658 |
| rs375611882 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147861647 | TGAGTAGCCTTTTTC[C/T]GCAGGCAGGTCGACG | 79658 |
| rs375617314 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147922461 | TTGGGAGGCCGAGGC[A/G]GGCGGATCACGAGGT | 79658 |
| rs375617939 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147734014 | GGAAGTAGGGGGGCG[C/G]CTATACATATGGAGG | 79658 |
| rs375623933 | snp | A/G | 8.26849e-05 | 0.00642928 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147913063 | TTAATGTTTTAAACT[A/G]TTTCTTGTAGATGCA | 79658 |
| rs375624209 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147971531 | GTTTCCCCAGTAAGT[C/G]TTTTGAATCAGTTTT | 79658 |
| rs375626245 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147946039 | TAGTCTAAGCCACTC[C/T]ACATTGATTTATTTC | 79658 |
| rs375626852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147899217 | CCAGCCTGTGTTCTA[C/T]CTTTAAAATTTTGTT | 79658 |
| rs375635751 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147905514 | CCATTGCTTGTTTTT[C/G]TCAGGTTTGTCAAAG | 79658 |
| rs375635904 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147842607 | ATGCCCTGAAATTGC[G/T]GTTTTCCCCTCTCCA | 79658 |
| rs375713338 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148016695 | ACACCGTCTACCTGG[A/T]GGTAGTGCCAGATGC | 79658 |
| rs375716892 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148069515 | CCTTTCACCTCCAGC[A/G]TTGTAGAAAATCACC | 79658 |
| rs375730015 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147963424 | CTTCTTTTCTGTCAG[C/T]AGTAAATTTAGAACC | 79658 |
| rs375732845 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147957140 | TTTGGATGACAGGAC[C/T]GTCAGAAAGAAATAC | 79658 |
| rs375738649 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147997500 | ATCAAAAGTTAAAAA[A/G]TGATCGTTGATGAAG | 79658 |
| rs375757687 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147821813 | AAGTCAGTCAACACC[G/T]TCTTAGAAAGTGCTT | 79658 |
| rs375758984 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147899134 | GCGCTTGAGGTCCCA[C/G/T]GGACAAGAGTTGGAG | 79658 |
| rs375762628 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147744291 | GGGAAAATGCATCTG[A/C]GAGGTCAGAGAGAGC | 79658 |
| rs375770285 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148061097 | TTCATGGAGGTTTCC[C/T]TTTTTTTTTTTAAAG | 79658 |
| rs375790277 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147989673 | AGGTTATCTCTCTTA[C/T]TCCCTGAACAATTGC | 79658 |
| rs375828968 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147891666 | CAGCTGCAAATGAAT[A/G]CCTACCATAGCTAAA | 79658 |
| rs375851420 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147758103 | CCCCGTCCATACTGA[A/G]AATACAAAAATTAGC | 79658 |
| rs375860595 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147803946 | TTCTTTGCCTTGGAT[A/G]AATATTCGATAGTGG | 79658 |
| rs375870169 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147785977 | CTCCTTTTACAGGTC[A/G]AACTTCTTTCTGATT | 79658 |
| rs375877461 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147915961 | TTTTTTTAAAAAAAT[C/T]AGCTGAGTGTTATAG | 79658 |
| rs375882230 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148034332 | AATTACTTATTTATT[A/T]TTTTGAGACCATTTC | 79658 |
| rs375888578 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147910190 | TTGTTTTTATTTTTA[A/T]TTTTTTTGTTGTTGT | 79658 |
| rs375897720 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147939622 | CATGGAACATTGTTT[A/G]CTGAGATTATTTTTT | 79658 |
| rs375903332 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147918285 | GGACTACAGGTGCCC[A/G]CCACGAAGCCTGGCT | 79658 |
| rs375909041 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147862031 | AGGAACCTGTCTCCC[A/G]CAGCTGTCAACATGT | 79658 |
| rs375920534 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147874775 | TAATGGTGTTAGAAA[A/G]CCTCCAAAGTAACCT | 79658 |
| rs375924397 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147847392 | ATTGGAAACAAAACA[A/G]AAACACCTGGACAAG | 79658 |
| rs375929177 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147810297 | GTGAAGTTGGAAACA[G/T]TTTTTGGTGTTTACT | 79658 |
| rs375942149 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147862464 | AACTCTGTAGAAGTT[G/T]GGGCTCCTGCCTGTT | 79658 |
| rs375944907 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148050726 | TCTAGGAATTCCACA[C/T]AATTAATCTTACCAT | 79658 |
| rs375947018 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147755312 | CAACTCAGTCTGGGC[A/G]TTCTGTGTTCATGGC | 79658 |
| rs375948908 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147809295 | CTGGCCCTGACCTCT[A/G]TCTGCAGCCGTTTGT | 79658 |
| rs375970955 | in-del | -/TC | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147982545 | TCACACCCAGCTAAA[-/TC]TTTTTTTTTTTTTTT | 79658 |
| rs375978340 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147864305 | GGGCGTCCAGCCCTG[G/T]CCCGCCTTTGAGAGC | 79658 |
| rs375983058 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147777477 | TGTGTTAGCCAGGAT[A/G]GTCTCCATCTCATGA | 79658 |
| rs375983176 | in-del | -/CTT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147770992 | CTTTGTCCTAATCTT[-/CTT]TTCTTTTAAGGAGAC | 79658 |
| rs375999672 | snp | A/G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147903693 | CAGAGTGTCATCTAC[A/G/T]TGAATCACACAGTGT | 79658 |
| rs376030073 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148008867 | TAAAACATTGAATGC[A/G]GAAGGAGACAGAGAG | 79658 |
| rs376045996 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147851567 | TAAATTACTACAAAA[C/T]ATGAGTAAAACTTAA | 79658 |
| rs376047482 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147981146 | TGGTTTCTTTAGGTA[C/G]AAGGTTAGGTTGTTA | 79658 |
| rs376054678 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148044092 | CTTCTACCAATGTTA[G/T]TTTCACTTGAGGGTT | 79658 |
| rs376059450 | snp | C/T | | | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148023320 | TGCCTGTCAGCATCA[C/T]CCCCAAATGCGCCAC | 79658 |
| rs376076170 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148070098 | CTAGGTGCTGGGTCT[A/C]ATGTTATATGTGTTA | 79658 |
| rs376084283 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147876788 | CTCATTTACTGTATA[A/C]CCAGCACTGTGCTAA | 79658 |
| rs376090626 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148002523 | CTCTGGTAGAATTCG[A/G]CTGTGAATCCATCTG | 79658 |
| rs376099595 | in-del | -/AG | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147751882 | CTTTCTGAAGCCTTT[-/AG]TTTTTTTTTTTTTTT | 79658 |
| rs376113964 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148000498 | TCCTTGAGGAATCGC[C/T]ATACTGTCTTCCACA | 79658 |
| rs376117366 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148002949 | AGTTATTTCTTGCCT[C/T]CTGCTAGCTTTTGAA | 79658 |
| rs376121208 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148063089 | GATTGGGATGTTGTG[C/T]ATTTCGTGTTCTGTG | 79658 |
| rs376124857 | snp | A/G | 5.02281e-05 | 0.00501114 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148047080 | CTTCTGTTGGGTGCT[A/G]AAGGGTGGAAGCCCT | 79658 |
| rs376127893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147770447 | TGAGAATTGCTTGAA[C/T]CCGGGAGGCGGAGAT | 79658 |
| rs376133028 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147987130 | AGTGGGGAAAGATAA[A/G]CATGGAGTATCACAT | 79658 |
| rs376147664 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148034352 | GAGACCATTTCGCTC[-/T]TGTTGCCCAGGCTAG | 79658 |
| rs376152015 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147975281 | TTGTACTGCCCAGAG[G/T]TGTCTTCATGGCACT | 79658 |
| rs376154933 | in-del | -/TC | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147977796 | AGTTTTTCCACCCTT[-/TC]TCTCTCTCTCCCCCT | 79658 |
| rs376180789 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147875747 | CTACGTGGCATCCTA[A/G]CTTGTAGGCTTTTTA | 79658 |
| rs376184015 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147892383 | CACATTAACTGTACT[A/G]ATATTTGTAAGCATT | 79658 |
| rs376191476 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148055874 | CGAACAGGGGAGCCC[C/T]GCACCACAAAACCAG | 79658 |
| rs376210972 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148016880 | CACATTTACTGATTT[C/G]TTATAAGGGACATTG | 79658 |
| rs376214095 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148048609 | ATCCTGGTTACACTC[A/G]AGGTGGAATTTAGCA | 79658 |
| rs376295305 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147773485 | CCAGAGACAGCTTGG[A/G]AAACAGTGTTATGTT | 79658 |
| rs376295950 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147827045 | TTTTATATTTGCCTC[A/G]GAAACCTTTAAAATA | 79658 |
| rs376297644 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147806692 | ACCCTGTGACAAACC[C/T]TTCAGGCGCCAGCAT | 79658 |
| rs376300493 | snp | C/T | 0.00209343 | 0.0322852 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147857521 | TGTATCCTTTTGTTT[C/T]TGTTTAATCATAGTT | 79658 |
| rs376302624 | in-del | -/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148045766 | AAAAAAAAAAAAAAA[-/G]AAATCCATCTAAGAT | 79658 |
| rs376308340 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147913156 | TAATATGATTGAATC[A/G]TTTCATTCATGAGAG | 79658 |
| rs376329700 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147923894 | ATATTTTACCAATTG[C/T]GCATTAATTTTAAAT | 79658 |
| rs376331684 | in-del | -/GT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147899329 | TGTGTGTGTGCATGC[-/GT]GTGTGTGTGTGTGTC | 79658 |
| rs376335765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147765652 | AAAAAATACAAAAAT[C/T]AGCTGGGTGTGGTGG | 79658 |
| rs376359991 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148027818 | AGAGAACAGAAAACT[A/G]GAAAGCAGGCCACTG | 79658 |
| rs376367084 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147969403 | AACTGTTATTAAGCC[-/T]CATTAGTGTGCACTA | 79658 |
| rs376373792 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147887974 | GAAGCCATCAGTGGT[C/T]TCCCTGTTGCTGTGC | 79658 |
| rs376378744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147917002 | TTTGAATCTCTCAGC[A/G]TATTCTCTGTGATTC | 79658 |
| rs376379627 | in-del | -/TGAATAGCCACTG | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147767679 | CCATGGTCATACCTG[-/TGAATAGCCACTG]CACTCCACTCTGGGC | 79658 |
| rs376436586 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147939370 | AAAAAAATTACAGTT[G/T]TGCTTTAGTTTTGAA | 79658 |
| rs376444544 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147920187 | TTTGGGAGGTCGAGG[A/T]GGGTGGATCACCTGA | 79658 |
| rs376444955 | snp | A/G | 0.00545396 | 0.0519349 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147881970 | CATGGTGAAAGAGTC[A/G]TTTTAAAAAAATGAT | 79658 |
| rs376461649 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147828103 | CCACTGTGCCCATTC[C/T]ACTTTATCTTTAAAA | 79658 |
| rs376464493 | in-del | -/CAAC | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147920124 | ACGTCTTTTAAAAAA[-/CAAC]ATAACCTCGCTGGGC | 79658 |
| rs376467032 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147861328 | GGTGGCACCCGGAAA[C/T]TTGGAGACACCAGGA | 79658 |
| rs376482269 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147787162 | TGTCACATAATCGGG[C/T]GCTGGAGGCTTTAGA | 79658 |
| rs376483857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147829435 | CTCGGGTGATCCACC[C/T]GCCTCGATCTCTGAA | 79658 |
| rs376496410 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147994011 | GAAGCTTGGAGAGCT[G/T]AAATTAACTTGCCCA | 79658 |
| rs376503689 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147789521 | GGTCTTGAACTCCTG[G/T]CCTCGGCCTCCCAAA | 79658 |
| rs376570896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147860643 | ATTTGAGAAAATTCC[A/G]TTTCTGTTTATTTTT | 79658 |
| rs376579848 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148040255 | CTTCTCCCAGTCCCT[A/G]TTTCCACATGAAGAG | 79658 |
| rs376580228 | snp | A/G | 0.000131874 | 0.00811909 | synonymous-codon, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148023274 | GAAGATTTTTCGGAC[A/G]CCGCCCGATACTACA | 79658 |
| rs376608570 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147878774 | ATTTTCCTTCTTCCT[C/T]TTTTTTTTTTTTTTT | 79658 |
| rs376615431 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147810791 | AGCCCACAGGGTTGG[G/T]TTCTTGCAAGATCTA | 79658 |
| rs376618897 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147922860 | ATGTGCCTCATTTGG[C/T]AGTTATATTGCCTGG | 79658 |
| rs376619524 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147839218 | GGAAAAACAAGAGCT[A/G]TGTTTTTGCTGAATG | 79658 |
| rs376644451 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148056720 | AGCTCAAATCCAGGA[C/T]GCCATGTTTCTATAA | 79658 |
| rs376646190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147884668 | AATTCATAAACTAAA[A/G]GGTTATCTGGAGTCA | 79658 |
| rs376658046 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147919613 | AGTCCCTCTCTGTTG[C/G]CCAGACTAGAGTGCA | 79658 |
| rs376658870 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147940326 | CTCAGGGATTCATTG[A/G]TATTCACAGTGGCTT | 79658 |
| rs376662608 | in-del | -/AT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147855417 | GAAAAGAGAGTAACT[-/AT]GTAATATCAATACAT | 79658 |
| rs376663697 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147840198 | CACCTTGCCAGGCAG[C/T]CTGTTTCATTATAGT | 79658 |
| rs376668926 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147765337 | TGGTGTGTGTGTGTG[-/T]GGGGGGGGGGGTGTG | 79658 |
| rs376673726 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148001948 | AGAACTTCCAACACT[A/G]TGTTGAATAGGAGTG | 79658 |
| rs376680661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147827955 | GGACTACAGGTGTGC[A/G]CCACCACGCCCAGCT | 79658 |
| rs376691784 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147764065 | ATGCCTGGCCCAGAC[A/G]GTGATTCTTGATCTT | 79658 |
| rs376701138 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147878811 | AGTCGGAGTCTCGCT[C/G]TGTTGCCCAGGCTGG | 79658 |
| rs376704901 | in-del | -/TATATATATATATA | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147798782 | CTCTCTCTCTCTCTC[-/TATATATATATATA]TATATATATATATAT | 79658 |
| rs376721213 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147815016 | AAGCCAAGAAGCTTA[A/G]AAGATTTGTTTGCCC | 79658 |
| rs376722085 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147784673 | AAAATATATATTATA[A/T]ATTATAAATATAAAA | 79658 |
| rs376729378 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147742577 | CAACCTCTGCCTCCC[A/G]GGTTCAAGCGATTCT | 79658 |
| rs376743706 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147861158 | GAGTGGCGAGGAGTT[C/T]GTGAGTGAGTTCAGG | 79658 |
| rs376751951 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147901132 | GTTTGAAATGTGTCC[A/C]ATGTTTCTCAAAGTC | 79658 |
| rs376753312 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147887442 | TTATTTCATTCATCT[A/T]AAAAAAACAAAAGCC | 79658 |
| rs376798554 | snp | A/G | 0.000404688 | 0.014219 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148023463 | TGTTGAGAGTATGGC[A/G]TATCATATGTCGTCA | 79658 |
| rs376804796 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147999148 | ATTGACCTGTAAACA[C/T]GGGGCTTGCAACTTA | 79658 |
| rs376816173 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147936398 | CAGTGGCGCAATCTC[C/G]GCTCACTGCAAGCTC | 79658 |
| rs376816269 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147778414 | TGCCATGACATGAGC[C/T]GCTTTCTCACAGTCC | 79658 |
| rs376831751 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147732713 | GCGGGCCCCGCCTGG[C/G]CCCCGCCTGGCCCCG | 79658 |
| rs376837777 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147872161 | AAACCTCTGAGGAAG[G/T]TGGGTGGTGAGGGAG | 79658 |
| rs376849784 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147931875 | AAAAGAAACTATCAC[A/C]AGAGCAAACAGACAT | 79658 |
| rs376885805 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147960676 | GCTTAATGAATTTTC[A/G]CATGTAATCAGCCCC | 79658 |
| rs376899579 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147913925 | TGGGAGGCTGCGGTG[A/G]GCAGATCACCTGAGG | 79658 |
| rs376906821 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147891155 | GAAATGAAAGCATAT[A/G]TTTACACAGAAACTT | 79658 |
| rs376913743 | in-del | -/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148041986 | CTCTCTGTGCGTGAC[-/T]TTCAGATCAATAAAA | 79658 |
| rs376928703 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147913447 | AGAAATTTATTTTCT[C/T]GTGGTTCTGGAGGCT | 79658 |
| rs376936590 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148067629 | GTCTTCCAGCCTCCA[C/T]AGATGCTCTTGCAGT | 79658 |
| rs376937823 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147751345 | AATGGTGGTGTTTGT[A/G]GTAGGAGTAGATAAT | 79658 |
| rs376938461 | snp | G/T | | | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147857564 | GTAGGAAGAAAAAAA[G/T]AAGTTTGACAAAGAG | 79658 |
| rs376948532 | snp | C/T | 3.32817e-05 | 0.00407919 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147866691 | TTTTGTGCTAATATC[C/T]CTTTTCTTCCTGTGT | 79658 |
| rs376955511 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147959614 | TGAGTGAGAACATGC[A/G]GTGTTTGGTTTTCTG | 79658 |
| rs376961217 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147867638 | TGGGAGGCCTAGGCG[A/G]GCAGATCGCGAGGTC | 79658 |
| rs376967435 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148071174 | AGTCAGAAGCCACTG[C/T]ACTTGCAAAGGCCTG | 79658 |
| rs376970919 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147971573 | TGAACAGGTGGAGAT[A/G]TTTTAAGAGGACATT | 79658 |
| rs376979891 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147999676 | CGAATAGAGCTCTAA[A/C]ACTCACCACATGGCC | 79658 |
| rs376990101 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148055712 | ACAAAATAAAGATAT[C/T]TGTTCTCAAAGGTGA | 79658 |
| rs376990540 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148045850 | CTAGGACCTGGGAGT[A/G]AGGAAACGTGAAGCT | 79658 |
| rs377012062 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148008565 | ATCCCTCCACAACAA[C/T]GACTTAGCAGTCCCC | 79658 |
| rs377050779 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147863283 | CTCCTGGCAGCCGTC[G/T]TTCTGCTTTCAGTTT | 79658 |
| rs377057007 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147832096 | CCGCCCGACATACAC[A/T]CACCCACCCACACAC | 79658 |
| rs377072076 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147927518 | TCACACTCTCTCACA[C/G]AGTCTCCATAAAACT | 79658 |
| rs377075004 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147895726 | TTCTTCCTTTCCAAT[C/G]TGTATGCTTTTTATT | 79658 |
| rs377079900 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148028383 | CTGGGCTGGGGAATA[C/T]GTATCCTGACTGTAT | 79658 |
| rs377083308 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148070447 | TCCTATTCATCCAGG[C/G]GAGGGAAGAACAAAC | 79658 |
| rs377087091 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147920640 | TCAACGTTGGTTACA[-/T]TACAATCCTTGATTT | 79658 |
| rs377095728 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147769356 | CATAACTCAAGATGA[A/T]CCCCTATTTAGAGAA | 79658 |
| rs377129201 | snp | G/T | 1.65168e-05 | 0.00287369 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147906757 | TTTTATTTCAAAGCC[G/T]TTAGAGTTGACTTGC | 79658 |
| rs377155132 | in-del | -/TTA | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147852729 | TTTTTTTTTTTTTTT[-/TTA]AAATGGAGCGGAGTT | 79658 |
| rs377162523 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147735176 | TACTGGAATTAGATA[C/T]GGATTTATAATGGGG | 79658 |
| rs377164392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148023155 | ATTTTGGGCTCTAGC[C/T]TGTCTTGAATGAACT | 79658 |
| rs377164521 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147846760 | ACATAATGTAGTCTG[A/G]TTATCAATAAAGGAA | 79658 |
| rs377181225 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147763263 | AGATGTACTAAAACA[A/G]GTTTGCTGGAATTAA | 79658 |
| rs377183745 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147876981 | AGTCTGTGTTGGTAA[C/T]GTCTCCCGTAAATTG | 79658 |
| rs377190962 | snp | A/G | 0.00010829 | 0.00735752 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147909709 | TGATTAAAAAATTCT[A/G]TTTTTCCATTCTCTT | 79658 |
| rs377192088 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147791371 | CCTGCCTCAGCCTCC[C/G]GAAGTGCTGAGATTA | 79658 |
| rs377198393 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147748427 | TTTTAGTTTTAGAAA[A/G]TAAGATCTGGAGATC | 79658 |
| rs377201330 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147820678 | TCACTGCAACTTTCT[C/T]CTCCTGGGTTCAAGT | 79658 |
| rs377207478 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147962733 | CCAGGCTGGAGTGCA[A/G]TGGTGCTGCAACCTC | 79658 |
| rs377209565 | snp | C/G | | | intron-variant, downstream-variant-500B | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147782740 | GCAAACAGGAAAGAA[C/G]AGACTTCTGGAAAAT | 79658 |
| rs377219087 | in-del | -/CTT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889672 | AACATACTTTGTCTT[-/CTT]TACAAGTATCTGTTT | 79658 |
| rs377219337 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147843651 | CCTACCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 79658 |
| rs377228106 | snp | G/T | 5.35652e-05 | 0.00517491 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147946747 | AGAATGGACTATTTG[G/T]ATCTGTAACATAAAA | 79658 |
| rs377235805 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148009593 | ATTTTGATGTTTCCC[A/T]GTCTGGAAGCCCTGT | 79658 |
| rs377253009 | in-del | -/GAGTGTGGGGTTGGCTGG | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147892594 | TGTGGGGTTGGCTGG[-/GAGTGTGGGGTTGGCTGG]AAGAGCTTACTAAAG | 79658 |
| rs377260181 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148030448 | TGTCAAGAGTGACTG[A/T]TTTGAAACGTTTTCT | 79658 |
| rs377270018 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147844469 | ACCCATTAACCATCC[C/T]TACCTCCCCCCTACT | 79658 |
| rs377272167 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147992697 | AGACGTGAGCCATTG[C/T]ACCTGGCCGAAAAAG | 79658 |
| rs377274065 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147826000 | CAGTGAAAAATGCTA[A/C]AAAACAATACAGGGC | 79658 |
| rs377276121 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147777135 | TGTTTTAAGGTGCAT[A/G]TGCATGATTTGCGTT | 79658 |
| rs377290627 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147843872 | CAGTTTCATTGCCAT[C/T]GTTTACCTCTGTTCT | 79658 |
| rs377292968 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147768824 | GTTCACTGCAGCCTC[C/T]GCCTCCTGGGTTCAA | 79658 |
| rs377313661 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147866983 | GTGTGACCAACTGCT[C/G]TACAGTTGGTTGAGG | 79658 |
| rs377340042 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148013220 | ATTAGAGCTGAAATG[C/G]AAATGGAAAAAAGAA | 79658 |
| rs377359183 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148002861 | GATCTTTTCAAAAAA[C/T]CAGCTCCTGGATTCA | 79658 |
| rs377364634 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148052190 | GGGAGTCACTGGCAA[A/G]CCCTGTCTTCACTTC | 79658 |
| rs377368852 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147972786 | TGAGACGGAGTTTCA[C/T]GCTTGTTGCCCAGGC | 79658 |
| rs377373402 | in-del | -/TATC | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147839093 | TGTTTAGATCTATCG[-/TATC]TATCTATCTATCTAT | 79658 |
| rs377375828 | snp | C/T | | | upstream-variant-2KB | ARHGAP10 | GRCh38.p7 | 4:147730225 | ATATATTTTCATTTC[C/T]TTTGGGTATATATCT | 79658 |
| rs377385890 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148025268 | TTAACTTCTTTAGTC[G/T]GGTTTTTATGTTCAT | 79658 |
| rs377415966 | snp | A/G | 0.000167344 | 0.00914572 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148046875 | TGTTTGATATTCAAT[A/G]CTTTTTTTCCTCCTA | 79658 |
| rs377433744 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147934492 | TGCCACTCCTCTATC[C/T]GTTAACGCTTTTGAT | 79658 |
| rs377446631 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147754959 | AATTAGCGGACGCCT[A/G]TAGTCCCAGCTACTT | 79658 |
| rs377471111 | in-del | -/GA | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147855192 | TAAGTCTGAGAAACA[-/GA]TGCTCAGAGAATGTT | 79658 |
| rs377481604 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147870220 | ACCTGCCACCATGCC[C/T]GGCTAATTTTTTTGT | 79658 |
| rs377483302 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147777321 | TGGAGTGCAGTGGCG[C/T]GATTTCGGCTCACTG | 79658 |
| rs377486235 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147759501 | ATCCCTTTAGGGCAG[C/G]AGTTCGAGGCTGTAG | 79658 |
| rs377492282 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147842095 | CCTGCCACCATGCCC[A/G]GCTAATTTTGTTGTA | 79658 |
| rs377496512 | in-del | -/ATA | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147784774 | ATGTATATTATAAAT[-/ATA]ATATATTATAAAATA | 79658 |
| rs377526131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147788979 | CCATAAACTTATCCG[A/G]TTCTTGCAGCAGCAG | 79658 |
| rs377544547 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147866148 | GATCACTTCTTTTTA[C/T]TTCTAGATTTATTGA | 79658 |
| rs377550326 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147951631 | TCAAAACATTAAAAA[A/G]AAATAGAAACAGGGT | 79658 |
| rs377553185 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147747083 | CCTCATGATACCCAG[A/G]AAGGCCGCTGTTTCA | 79658 |
| rs377558707 | snp | A/G | 6.61989e-05 | 0.00575283 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147864842 | CTCTGTGATTTTAAC[A/G]TAGGCAGATATCCAA | 79658 |
| rs377561565 | snp | C/G | 3.29506e-05 | 0.00405884 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148046972 | TCTCCCGTGACTACA[C/G]CTGTCCCTGGGCCTC | 79658 |
| rs377563209 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148014142 | ATAGTTGACATAGAG[C/T]ATATTTTATTAATGT | 79658 |
| rs377563428 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147863438 | GAATTTCCTTCCTGT[C/T]TAAGGCTGAATAATA | 79658 |
| rs377570053 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147938527 | CCCTCCCAGCATAAC[A/G]TAGGGTATAGGATGC | 79658 |
| rs377571271 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147861942 | GAACTGGCAGCCCAG[C/T]GGCTCCCAGGCTTCA | 79658 |
| rs377580783 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147773581 | CAAACTGACATTGTA[A/G]TGTTTTCCAATATGT | 79658 |
| rs377591925 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148028887 | AAAGTGGACATTATT[C/T]GCCACAGATTAGGCT | 79658 |
| rs377591998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147755030 | GAGGTTGCAGTGAAC[C/T]GAGACTGCGCAGTTG | 79658 |
| rs377615176 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147896227 | TAAGATGGCTACAGA[A/G]GAATTGGGAAGTTTT | 79658 |
| rs377618287 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147836191 | CTTGTTCGTAGAAGA[C/T]AGATACTAAGAGAAT | 79658 |
| rs377621044 | snp | G/T | 0.0178098 | 0.0926698 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147814302 | GCATCTTTTTTTTTT[G/T]TTCCAAGCTTTAAAT | 79658 |
| rs377621378 | snp | A/G | 4.95585e-05 | 0.00497763 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147881822 | TTTTGAGAATGTTCA[A/G]AATGATTATTTGCAG | 79658 |
| rs377622821 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147830787 | GGTCTGCCAAAGTGT[-/T]GGGATTACAGATGTG | 79658 |
| rs377626837 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147867047 | GCAGTTTCTGGGTCA[A/G]TTCTAAGGATAAGCT | 79658 |
| rs377654628 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148005170 | GGGTCTTTGCACTTA[C/T]TTGTTTATTCCCAGT | 79658 |
| rs377655971 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148024443 | TGCATGCACACACCA[A/G]GTGGTTAATATCCAG | 79658 |
| rs377665324 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148036407 | TAATCCCCACGTGTC[A/G]TGGGAAGGACCCAGT | 79658 |
| rs377665735 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147930418 | AGGCTAAGGACAAGT[G/T]GAGGTATTAAGAATA | 79658 |
| rs377701328 | snp | C/T | 1.79832e-05 | 0.00299854 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147866867 | TTGAAAAGTATTTTT[C/T]ATTTGTGTGTTGTAT | 79658 |
| rs377705863 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147783817 | TATTTATATAACACA[C/T]ATTAAATTGTGTATT | 79658 |
| rs377707350 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147959878 | TGAATCCTAAAGTAT[C/T]TAAACTAGGTTTTCA | 79658 |
| rs377712275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147980449 | TTTACTAGTATTTTG[C/T]TGAGGATTTTTGCAT | 79658 |
| rs377735676 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147912568 | ATATATATATATATA[G/T]ATATATATATATATA | 79658 |
| rs377754979 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148031777 | CAGAGAGGACTATGG[A/T]TTTCAATGTGGGACA | 79658 |
| rs386401815 | in-del | -/TT | | | upstream-variant-2KB | ARHGAP10 | GRCh38.p7 | 4:147730886 | TTTTTAAGAAATACT[-/TT]TTTTTTTTTTTTTGA | 79658 |
| rs386401816 | in-del | -/TT | | | upstream-variant-2KB | ARHGAP10 | GRCh38.p7 | 4:147730898 | ACTTTTTTTTTTTTT[-/TT]TGAGACATTGTCTCG | 79658 |
| rs386401817 | in-del | -/AAA | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147785084 | GACGACTATTTTCTA[-/AAA]AAAAAAAAAAAAAAA | 79658 |
| rs386401818 | in-del | -/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147787453 | GGAGTGATGGAAGCG[-/G]GTGGGGGAGGAGGCT | 79658 |
| rs386401819 | in-del | -/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147787454 | GAGTGATGGAAGCGG[-/G]TGGGGGAGGAGGCTC | 79658 |
| rs386401820 | in-del | -/A | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147920642 | AACGTTGGTTACATA[-/A]CAATCCTTGATTTAT | 79658 |
| rs386680611 | multinucleotide-polymorphism | CGGGCGCGGTGGCTCACGC/TGGGCGCGGTGGCTCACGG | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147738273 | TAGAAATTGTAGGGC[lengthTooLong]CTATAATCCCAGCAC | 79658 |
| rs386680612 | in-del | ACAAA/CC | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147751189 | ACCTCAAAACCAAAA[ACAAA/CC]AAAAACAAACAATGA | 79658 |
| rs386680613 | in-del | G/TGT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147765335 | TGTGGTGTGTGTGTG[G/TGT]GGGGGGGGGGGTGTG | 79658 |
| rs386680614 | multinucleotide-polymorphism | CT/TG | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147776114 | ATCATTTATGGCCTC[CT/TG]CGTAATCATTAACTT | 79658 |
| rs386680615 | in-del | AA/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147832360 | TTTTTTTTTTTTAAA[AA/C]GAGGAGTCCAGGCAC | 79658 |
| rs386680616 | in-del | ACCCATACACATACCCACCCACT/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147834700 | CACACTCACACCCAC[ACCCATACACATACCCACCCACT/C]TCCACCCGCACACCC | 79658 |
| rs386680617 | multinucleotide-polymorphism | AT/GC | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147867841 | TGCACTCCAGCCTGG[AT/GC]GACAGAGTGAGACTC | 79658 |
| rs386680618 | multinucleotide-polymorphism | CAGTTCATGCCATCCTC/TAGTTCATGCCATCCTT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147870174 | TCCTGCCTGTAGTCC[lengthTooLong]CTGCCTGTAGTCCCA | 79658 |
| rs386680619 | multinucleotide-polymorphism | CCC/GCA | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147887243 | CTCAGTGCCCAGACA[CCC/GCA]TGCCTTTCCTCCCTG | 79658 |
| rs386680620 | multinucleotide-polymorphism | ATC/GTT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147887550 | ATTCTTCAAAAAGCT[ATC/GTT]ATATTTATGGTCTCA | 79658 |
| rs386680621 | in-del | AGGCT/TAGTTTGA | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147898183 | TCCTTAGGCTGCCTT[AGGCT/TAGTTTGA]GCATTTCTTGTAATG | 79658 |
| rs386680622 | in-del | CTGTGTGTC/GTG | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147899357 | TGTCTGTGTCTGTGT[CTGTGTGTC/GTG]TTTGTCTTCTGTCCA | 79658 |
| rs386680623 | multinucleotide-polymorphism | CT/GC | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911594 | GTCTTGATCTCCTGA[CT/GC]TCGTGATCCGCCCAC | 79658 |
| rs386680624 | multinucleotide-polymorphism | CGC/TGT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911651 | ACAGGCGTGAGCCAC[CGC/TGT]GCCTGGCCTCTTAAC | 79658 |
| rs386680625 | in-del | A/CTG | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147920199 | AGGTGGGTGGATCAC[A/CTG]AGGTCAGGAGTTTGA | 79658 |
| rs386680626 | multinucleotide-polymorphism | ATC/TTT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147920212 | ACCTGAGGTCAGGAG[ATC/TTT]GAGACCAGCCTGGCC | 79658 |
| rs386680627 | multinucleotide-polymorphism | CA/TG | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147967513 | GACCCAGGTGATCCA[CA/TG]TTGGGGTGAGCAGAA | 79658 |
| rs386680628 | multinucleotide-polymorphism | AT/CC | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147994381 | AAAGTTCTTGTTAAT[AT/CC]TTGCACAGCTGGTGT | 79658 |
| rs386680629 | multinucleotide-polymorphism | CA/TG | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147999468 | CTGCCATTGCAGCCC[CA/TG]CCACTGACTTCCATC | 79658 |
| rs386680630 | multinucleotide-polymorphism | CA/TG | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148052079 | TACACCACAGTAAAC[CA/TG]TGAATGATTTGCCTA | 79658 |
| rs397688339 | in-del | -/GA | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148060037 | GAGACGAGAGAGAGA[-/GA]CGAGAGACAGATATG | 79658 |
| rs397701376 | in-del | -/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147947959 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTTGC | 79658 |
| rs397718223 | in-del | -/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147828894 | GTTTTTTTTTTTTTT[-/T]GAGATGGAGTTTCGT | 79658 |
| rs397719824 | in-del | -/A | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147825458 | CTCAAAAAAAAAAAA[-/A]GTGACAGAGACATAT | 79658 |
| rs397721100 | in-del | -/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147836655 | GGGTTCCTTAAATCT[-/T]AAGTACCAAGTAAGC | 79658 |
| rs397723763 | in-del | -/A | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147906556 | AAAGTAAAAAAAAAA[-/A]TGGTTACAACAGTTA | 79658 |
| rs397729170 | in-del | -/TT | 0 | 0 | upstream-variant-2KB | ARHGAP10 | GRCh38.p7 | 4:147730899 | CTTTTTTTTTTTTTT[-/TT]GAGACATTGTCTCGC | 79658 |
| rs397731212 | in-del | -/AAAA | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148065996 | AAAAAAAAAAAAAAA[-/AAAA]GGGTTGAGGGGATTA | 79658 |
| rs397734422 | in-del | -/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147742918 | CTTTTTTTTTTTTTT[-/T]AAAGTTTTGGGGACA | 79658 |
| rs397736029 | in-del | -/A | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148071647 | ACAAACAAAAAAAAA[-/A]CACAAAAAGCTTGAG | 79658 |
| rs397744134 | in-del | -/A | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147838483 | CTCTTAAAAAAAAAA[-/A]CACACACACACACAC | 79658 |
| rs397748841 | in-del | -/TCTT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147917843 | TTACTCAGAGGTCTT[-/TCTT]AAAGTCGCATTTATT | 79658 |
| rs397756785 | in-del | -/A | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147899727 | TCATCTCTGGAAAAA[-/A]ATGCATGATTCATAG | 79658 |
| rs397760907 | in-del | -/CT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147825190 | CAGTGGCTGATGCCT[-/CT]GTAATCCCAGCACTT | 79658 |
| rs397769448 | in-del | -/A | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147780567 | AGACTAGGAAAAAAA[-/A]GACTGAACTGTATTA | 79658 |
| rs397773210 | in-del | -/A | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148071646 | AACAAACAAAAAAAA[-/A]ACACAAAAAGCTTGA | 79658 |
| rs397782129 | in-del | -/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147848104 | AGTTTTTTTTTTTTT[-/T]CTCTTCCTAAAAGAA | 79658 |
| rs397782997 | in-del | -/C | 0.375 | 0.216506 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147759592 | ACCGCCCCCCCCCCC[-/C]TTTAAAAAGGAAACA | 79658 |
| rs397790338 | in-del | -/A | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147910361 | TCAAAAAAAAAAAAA[-/A]TTGTACAAAATACTT | 79658 |
| rs397790912 | in-del | -/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147857544 | CATAGTTTTTTTTTT[-/T]ATTTGTAGGAAGAAA | 79658 |
| rs397797044 | in-del | -/A | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147899728 | CATCTCTGGAAAAAA[-/A]TGCATGATTCATAGA | 79658 |
| rs397801198 | in-del | -/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147983203 | TTTTTTTTTTTTTTT[-/T]GAAGCAGAGTCTCAC | 79658 |
| rs397802606 | in-del | -/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147753367 | TTCTTTTTTTTTTTT[-/T]GAGACACAGTCTGTT | 79658 |
| rs397820915 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147914597 | ATCTTCAGCATTTTT[-/T]GTACAAATGGAATCA | 79658 |
| rs397827198 | in-del | -/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147949848 | ATTGCATTCTTTTTT[-/T]CCTCCATTCCGTATG | 79658 |
| rs397878485 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147870932 | CCAAAACTACAGACT[A/G]TGTGTGTGTGTGTGT | 79658 |
| rs397879078 | in-del | -/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147759591 | CACCGCCCCCCCCCC[-/C]CTTTAAAAAGGAAAC | 79658 |
| rs397879283 | in-del | -/A | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147737485 | GATAAAGTGGTGTAA[-/A]TTGTAAATTTTGTGA | 79658 |
| rs397879701 | in-del | -/CT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148014771 | CTGCTATGCATCACT[-/CT]ATTTAGCGTATAGAG | 79658 |
| rs397880050 | in-del | -/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147891963 | GTGCTGTGACCCCCC[-/C]ACACATTTGCTTGAT | 79658 |
| rs397880270 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147877272 | GTGCAATATTTTTTT[-/T]GTCAACCATAGAACA | 79658 |
| rs397880416 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147793333 | ATATTTTTTTTTTTT[-/T]ACAAATGTACAGTTG | 79658 |
| rs397881300 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147858352 | AATTGTATTTTTTTT[-/T]CTTGTTTTTTTAACA | 79658 |
| rs397946808 | in-del | -/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147761897 | TGGACTTTATGTAGC[-/C]AGTAACAGCAGCAAC | 79658 |
| rs397947218 | in-del | -/A | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147748392 | AACTAGTAAAAAAAA[-/A]GCTGATGTCTTGTAC | 79658 |
| rs397963595 | in-del | -/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148038425 | TTTATAATCCCCCCC[-/C]ATTTCAGGTTCTTCC | 79658 |
| rs397969316 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147750614 | TCTTTTTTTTTTTTT[-/T]GGGGGGGGTTGTAAT | 79658 |
| rs397995733 | in-del | -/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147815735 | GTGGTGGTGGTGGTT[-/T]CATGCCTGTAGTCCC | 79658 |
| rs397995734 | in-del | -/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147827192 | ACTTTTTTTTTTTTT[-/T]AAAGTGGAATCACTG | 79658 |
| rs397995735 | in-del | -/TT | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147867939 | AACTTTTTTTTTTTT[-/TT]ATGTACAGTTCCTTA | 79658 |
| rs397995737 | in-del | -/G | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147894143 | GCATAAATACTTTGG[-/G]TGTGGGAATTGCTGG | 79658 |
| rs397995738 | in-del | -/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911949 | TAGGTTTTTTTTTTT[-/T]AAAGGATTGTGTTCT | 79658 |
| rs397995739 | in-del | -/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147919576 | AAAACAATTTTTTTT[-/T]CTTTTTTTTTTGTGG | 79658 |
| rs397995742 | in-del | -/A | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148018587 | AAAAAAAAAAAAAAA[-/A]GGCTTCAGAACTGGG | 79658 |
| rs398083620 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147858351 | AAATTGTATTTTTTT[-/T]TCTTGTTTTTTTAAC | 79658 |
| rs398083621 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147877271 | TGTGCAATATTTTTT[-/T]TGTCAACCATAGAAC | 79658 |
| rs398083622 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148061624 | TAATGTTTTTTTTTT[-/T]TAAATGACCCCCTTT | 79658 |
| rs398108114 | in-del | -/A | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147887449 | TTCATCTTAAAAAAA[-/A]CAAAAGCCACTACAG | 79658 |
| rs483352827 | snp | A/T | | | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147875034 | AGACACGGAATCGAT[A/T]TGAAGGAACAAGGTC | 79658 |
| rs483352828 | snp | C/T | | | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147965041 | AGCGGCAGCCCAGAA[C/T]CTCGTGTTAATGCGA | 79658 |
| rs483352829 | snp | A/G | | | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148064463 | CGTGTGAAGCAGAAC[A/G]CAGCTCGGAATTATC | 79658 |
| rs483352830 | snp | C/T | 1.68752e-05 | 0.00290471 | ARHGAP10 | 4 | allele_origin=T(somatic)/C(germline) | 4:147875140 | AGGCTACCTGTATGT[C/T]CAGGAAAAAAGTAAG | 79658 |
| rs483352831 | snp | A/G | 3.30044e-05 | 0.00406216 | ARHGAP10 | 4 | allele_origin=G(somatic)/A(germline) | 4:147906740 | AATAATCAATGGTTG[A/G]GTTTTATTTCAAAGC | 79658 |
| rs527244191 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147947590 | GTAATTTTAGTAGAG[A/G]TGGGGTTTCGCCATG | 79658 |
| rs527246330 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147878038 | GCCTCCTGGGTTCAA[A/G]CCATTCTTCTGCCGC | 79658 |
| rs527254785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147794969 | ACGTTTTGAGGTTTC[C/T]AGCTGCTTTTGCAGT | 79658 |
| rs527268053 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148066547 | TAAAAAGAAAGTGTG[C/T]GTGTACACACGTACA | 79658 |
| rs527303692 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147974983 | ACTGGGTCCCTCCCA[C/T]AACATGTGGGAATAT | 79658 |
| rs527304026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147968309 | AAGAAAAATGCTGCT[A/G]ACTCATAGTTAAAAG | 79658 |
| rs527307147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147843477 | TGAGCTCTCATTCTT[C/T]CTTTAAAACGTCTCT | 79658 |
| rs527328766 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147927691 | CTTATCCTATGGCAG[C/T]AGAAACAGGGTGAGA | 79658 |
| rs527330081 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148010899 | TTTTTAATAGAAAAA[A/T]TGCCCCAATCCAGGA | 79658 |
| rs527338570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147754077 | GGCAGTGTCTGTCTT[C/T]CGTCCTCCAGCAGTG | 79658 |
| rs527341911 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147935376 | CAGAATGGATTATAG[A/T]TGTGTGTTTCTTTTT | 79658 |
| rs527346567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148024243 | GAGGCCTTCCTCTTA[C/T]TGAGAACATTTGCTG | 79658 |
| rs527369320 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147850488 | GACCATGAACCCAGC[A/G]GGAGGAACAGACAAC | 79658 |
| rs527398054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148024805 | CTGACTGTTTTGAAT[C/T]GCACCTTCTCTTACA | 79658 |
| rs527399860 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147879921 | TATACAATGGAACTG[A/G]CTTGCTGTTCATAGC | 79658 |
| rs527402377 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147761078 | CTGGAGTGCAGTGGT[A/G]TGATCATAACCCACT | 79658 |
| rs527403067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147941783 | AATACCATTTTCTTA[C/T]TACCTTATGCTACCA | 79658 |
| rs527407064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147849993 | ACTTTTCTGTCTAGC[C/T]AAAGGATTGTAAACG | 79658 |
| rs527407368 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | ARHGAP10 | GRCh38.p7 | 4:148072855 | GAATTGGCAGCCTAC[A/G]ATGGGGACTCGTCTC | 79658 |
| rs527416535 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147917610 | GCATAAACAAAGGAG[A/G]TCATTTTAACTTAAG | 79658 |
| rs527422366 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147808505 | GGTTTTAAGCAGGGG[A/T]GTAAGGAGATCCAAT | 79658 |
| rs527425225 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147981666 | GTGTTGAAGTCTCCT[C/G]CTATTATTATGTGGC | 79658 |
| rs527433693 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148045252 | CCATCACCACCATCT[C/G]TAACTCCTGCTTGTC | 79658 |
| rs527449149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147941078 | AAGAATTTAATGGGA[A/G]TACAGCATCTGCTTT | 79658 |
| rs527457062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147863461 | GAATAATATTCTGTT[A/G]TACATATGGATTGGC | 79658 |
| rs527465164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147987484 | ATTTGGTACAAGTAT[C/T]TCCTTCAGGCGACAG | 79658 |
| rs527466973 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147829157 | CTGGGTTCAAGCGAT[A/T]CTCCTGCCTCAGCCT | 79658 |
| rs527472618 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147807624 | TAATCCAAAAAAAGG[A/C/T]CATAAAGAGGAAAAT | 79658 |
| rs527493123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147988294 | ATTTTTCAGTTTTCT[C/T]AGCCCACAGTTTAAA | 79658 |
| rs527498508 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147900919 | GCAATCCTCCTGCCT[C/T]AGCTTCCCAAAGTTT | 79658 |
| rs527509446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148031602 | ATTGCCATTTGTCTT[A/G]TGGTTCCTTTCAGAG | 79658 |
| rs527516320 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147907436 | ATGTATGACTCTAAA[C/T]AAACTGCCATTGCAG | 79658 |
| rs527518338 | in-del | -/TC | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147861006 | TTTTCCAGCCAGAAA[-/TC]TCTGTGTCTGGTGAT | 79658 |
| rs527535408 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148045851 | TAGGACCTGGGAGTG[A/C]GGAAACGTGAAGCTT | 79658 |
| rs527538187 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147772129 | TTAAGGGGATCTCTC[C/T]TGAGAAGTTCTCTCT | 79658 |
| rs527551993 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147800315 | CTACCTGTGCCCCAC[A/G]GTTTTCCTCATGTCT | 79658 |
| rs527552105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147821475 | AAGTTTTACAGTTTT[A/G]CCTTTTCATATTTAG | 79658 |
| rs527556309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148037503 | ATTTGAGGAAACAGT[A/G]TGGTGCACTCTACTC | 79658 |
| rs527567831 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147992761 | ACTTCTGCCATCCAG[G/T]ATTAGTGCCATTTTC | 79658 |
| rs527577069 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147871401 | TTCGTGTCCGTCTCT[C/G]TATTTTACAATGATA | 79658 |
| rs527578080 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147774641 | GGGTGACCACCCAGG[A/C]TTTACAAAGCTTCTT | 79658 |
| rs527590661 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147780376 | GCATGCGGTCACATT[A/C]CTGGGAGTGACAGTA | 79658 |
| rs527605260 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147797081 | CATCCGGCCTGGAGC[A/C]TGGCATATCATGGGG | 79658 |
| rs527613209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147993838 | TCCTAAGCATTCTAG[C/T]CTGCTTGGGGGAGAG | 79658 |
| rs527613694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147954620 | AAAGGCTGTACAGAC[C/T]GACACTTGTCTAGGT | 79658 |
| rs527616399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148000336 | TATCATTGATGGACA[C/T]TGGGGTTGGTTCCAA | 79658 |
| rs527664237 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147896316 | TAATTCACCTATGAA[A/G]TCATCTTTGCCTAGA | 79658 |
| rs527671140 | in-del | -/TTCT | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147818156 | TATTTTTTTTTCTTC[-/TTCT]TTTTCTTTTTTTTTT | 79658 |
| rs527675640 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147809903 | GCTATACGCCAAGGA[G/T]ATTTAGGATAACGCT | 79658 |
| rs527687437 | in-del | -/TTTGT | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147797412 | ACGTACCCTCCCCAC[-/TTTGT]TTTGTTTTGTTTTGT | 79658 |
| rs527688091 | in-del | -/T | 0.0107246 | 0.0724382 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147909643 | GCTTATAAAAATGTA[-/T]TTTTTTTTGTATGGT | 79658 |
| rs527689986 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147809420 | TCTTTTTAATGGTTC[C/T]ACCAATCTTTGTCAT | 79658 |
| rs527692973 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147990332 | AACTAAACATTTTGA[C/G]GAATGAATGTTAGCC | 79658 |
| rs527695247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148067156 | ACTTGTCTTGTAGGT[A/G]CCGCCCTGATTCTTT | 79658 |
| rs527696448 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147983386 | GAGACAGGGTTTCAC[C/T]GTGTTAGCCAGGATG | 79658 |
| rs527710492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148049364 | CAGGGCTGTGCTGAG[C/T]ATAAGCTGCTTCTCT | 79658 |
| rs527719502 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147769883 | AGAGGAGCCTGAAGG[C/G]ACTGCCACTTTTCTC | 79658 |
| rs527723799 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147859511 | ACTCCTGACCTCAGG[C/T]GATCCACCCACCTTG | 79658 |
| rs527731201 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148025918 | ATTTTTCCAAATGTT[A/C]TAGTTTATATGGGAC | 79658 |
| rs527735844 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147902276 | GTCCATTCTCCACCC[A/G]GCAACCAGACTGTTC | 79658 |
| rs527744651 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147909008 | ATCCCACATGTTTAG[A/T]GCTCACTCCCACAAG | 79658 |
| rs527747117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147824493 | ATTAGTCCGTTCTTA[C/T]AGTGCTATGAAGAAA | 79658 |
| rs527750776 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147816387 | TGGGTTTCTTTTGGG[G/T]CCTATGCACCTTTGT | 79658 |
| rs527752939 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148039908 | TGGCAATTTCACTTC[G/T]ATTCTCTATATTACA | 79658 |
| rs527760020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147864750 | ATCAGGCAGCACACC[A/G]TATTTTGGCCCATGG | 79658 |
| rs527780379 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147769292 | AGGTAATTAGGGAAA[A/T]TACTCAGTAAATGTT | 79658 |
| rs527780632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148001348 | GAAGTCAGGTAGCGT[A/G]ATGCCTCCAGCTTTG | 79658 |
| rs527784310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147776337 | CAATTCTCCTGCCTC[A/G]GACTCCTGAGTAGCT | 79658 |
| rs527797288 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147775959 | AGGCATAGAAAAGTT[A/C]CGTAAGCTGGCTATG | 79658 |
| rs527808877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147820701 | GTTCAAGTGATTCTC[A/G]TGCCTCAGCCTCCCA | 79658 |
| rs527809623 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147949416 | AATTAGAACAGTGTT[C/T]CTCAACTGAGGATGG | 79658 |
| rs527838306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147871376 | TGTTTTTGCCCCCCA[A/G]GTAGGACTATTCGTG | 79658 |
| rs527840757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148006647 | TACTTCCTATTGACT[C/T]CCAGAAGAGAGTACT | 79658 |
| rs527841006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147735592 | AAGGTTAGGAATGTG[A/G]ACTTTATCTTGTGGA | 79658 |
| rs527855520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147781739 | CTGGAGTGCAGTGGC[A/G]CAATCTCGGCTTAGT | 79658 |
| rs527858006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147823490 | TGGCCAGGCATGGTG[A/G]GTCATGCCTGAAATT | 79658 |
| rs527858923 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147941961 | AGTGTTCAAATGGAA[A/G]TAATTTAACGCCTCT | 79658 |
| rs527880103 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148046809 | TCATTTGATTGACTA[A/C]TCAAGTAACACCATA | 79658 |
| rs527881596 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147962491 | GAGAGGTTAGTTAGG[G/T]AATTTGTTCAAGACC | 79658 |
| rs527885383 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147908503 | GACAAAGGCAAGTCT[G/T]CAGAAAAACAATATT | 79658 |
| rs527917143 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147914138 | GCCTGGGTGATAGAG[C/T]GAGATTGCATCTCAA | 79658 |
| rs527917171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148047120 | CATTTTAAAGTTTCC[A/G]TGAGCAGTGACCTGT | 79658 |
| rs527919549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147830600 | TCTTGGCTCACTGCA[A/G]CCTCTGCCTCTCATG | 79658 |
| rs527923791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147742375 | CTATGGTAGGTGCCT[A/G]TTATTTTTATTATTA | 79658 |
| rs527923866 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147733142 | GCGGGCACTGCTTGC[A/G]AATAGGGAATTCCAC | 79658 |
| rs527932340 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147734896 | TATTTATATTTCCAG[A/C]TATTTTATATTTTAT | 79658 |
| rs527932791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147830086 | TTGTCCACGGCTGCA[C/T]CCCTTTCCCCATTTG | 79658 |
| rs527947070 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148053842 | GTACTTGGCACTTGC[C/G]TGTGGCCTAATTCGT | 79658 |
| rs527952136 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147920732 | TTGCAAATTTGCACC[A/G]ATTAAGAGAATATGA | 79658 |
| rs527963147 | in-del | -/AACT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147736045 | GAGAAAATTTTTTAA[-/AACT]AACAGTCCTTACAGT | 79658 |
| rs527974298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147781219 | AAAATTTAGCTGTGC[C/T]TGTAGTCCCAGCTAC | 79658 |
| rs527987254 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147927955 | GTCGCTTTCCTCTAG[A/G]CCCTGTCTCGGCACT | 79658 |
| rs527988368 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147919638 | AGTGCAGTGGCATGA[G/T]CTTGGCTCAGTGCAG | 79658 |
| rs528003175 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147843982 | ATGCCATCTACTTGC[G/T]GATGAGGACAAAATT | 79658 |
| rs528008619 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148006278 | TGTTCCAGCTTTCCT[G/T]TCCAGGCACTGGACA | 79658 |
| rs528013198 | in-del | -/A | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147894366 | GTTTCTTCTGTCATG[-/A]AGTGTCTATTAAAAT | 79658 |
| rs528016474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147876448 | AATACAAAAAATCAG[C/T]AGGGCGTAGTGGCGG | 79658 |
| rs528026586 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147769559 | TTCCGTATGTTAACA[A/G]GTTCTTTCTACAGAG | 79658 |
| rs528047003 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147948671 | ATTTCAAGAATGCAT[G/T]GTAGGCCGGGCGCGG | 79658 |
| rs528049664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147777086 | TGTTACAGTCAGTTT[C/T]CTTCTTGGACATAAA | 79658 |
| rs528072412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147818093 | ACTTATTACCAGCAG[C/T]GTAAAGAGGTCTGTG | 79658 |
| rs528072870 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148049113 | TGATGAGTGTGTATC[A/C]GTCCAGATTTGTCAT | 79658 |
| rs528073303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147964364 | TACAGTAGAGGCTTT[A/G]CCCGCATTCCCCGTT | 79658 |
| rs528073566 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147756397 | CACACTCTAGAGTGG[A/G]CATCTCAGGAGTGTT | 79658 |
| rs528074898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147910277 | ATCCTCCTACCTCTG[C/T]CTTCCAAAGTGCTGA | 79658 |
| rs528085231 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147829813 | TTACTTCTCTACATG[A/T]ATTCTTTTATCAGAT | 79658 |
| rs528092439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147957458 | GTCTCCCCTTTTGAA[C/T]GCTGTTGGAAAATCG | 79658 |
| rs528101769 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147825636 | TCATGTGATCCTGTA[C/G]TCATCAATTTTTCAG | 79658 |
| rs528107674 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147977328 | CAGGGAAGGCACCAT[C/G]AGGTGCCTTTTCTTG | 79658 |
| rs528111566 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147946488 | AGAGAAATCATATAT[A/G]TAATGTTTTCCTAGG | 79658 |
| rs528116883 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147737414 | TCCACCTCGGCCTCC[A/C]AAAGTGCTGGGATTA | 79658 |
| rs528129509 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148041886 | TTAAAGAAAAGCCAG[C/T]TCTCTTGGCCGGGAG | 79658 |
| rs528157409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147915475 | AAAAGGGCATGTTTT[A/G]TACATACTTATTTCT | 79658 |
| rs528166091 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147872446 | CAAATATATAGGTAG[A/T]TAAAGAAGTAGTGAT | 79658 |
| rs528183264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148007255 | ATAATCAGAATAAAA[A/G]GAACATTAAGATGAG | 79658 |
| rs528187742 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147824384 | TACTATCTAGAATTA[C/T]GTTATAGTGTAAGTG | 79658 |
| rs528192621 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148007605 | GCTCCCAGTCTTAAC[C/T]TTGTAAAACTTTGCT | 79658 |
| rs528197026 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147922468 | GCCGAGGCGGGCGGA[A/T]CACGAGGTCAGGAGA | 79658 |
| rs528204509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147877996 | GGCTGGAGGGCAGTG[A/G]CACGATCTCATCTCA | 79658 |
| rs528207188 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147759046 | GTCTATTTTCTTCAA[C/T]GCAAGGTTCATGGAG | 79658 |
| rs528207690 | in-del | -/A | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148030116 | TTTCTGTGGAGGAGG[-/A]AAAAAAAAAAAGCTT | 79658 |
| rs528209509 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148002156 | AAAGACCTTTTTTGC[A/C]TCTATTGAGATAATC | 79658 |
| rs528236145 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147884515 | TTCCTCCCCACCTTT[C/T]AGCTTCCGTCTTTTT | 79658 |
| rs528253657 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147750514 | TTCTTTAAAGGGAAT[A/C]GTCATCACCCAACCT | 79658 |
| rs528258628 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147838892 | GTTTTTGTAACTTAG[G/T]CCTGTTTGTAATCTC | 79658 |
| rs528260483 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147976944 | CAGTACTTGCCATGA[C/G]GTGAGTTTTTGATTC | 79658 |
| rs528273188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148062733 | GAGCAGGTGAAAGAT[C/T]TTTAAATGTTTAGCT | 79658 |
| rs528290065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147883921 | GCTGGTCTTGAACTC[C/T]TGACCTCAAGGGATC | 79658 |
| rs528304498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147803722 | TTTTACTTAATATAA[C/T]GACCTCCAGTTCCAT | 79658 |
| rs528308853 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148064564 | GGATTAATAAGTCTG[C/T]AGCATGGAGTGAGCA | 79658 |
| rs528310445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148055572 | TATGCACCTGTAATC[C/T]CAGCTACTCGGGAGG | 79658 |
| rs528315747 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147929960 | ACATGTGTGTATATA[C/T]ATGCACATGTGCCTC | 79658 |
| rs528332350 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147852654 | CCATGGGCCGATTGA[C/G]GTAAACAAAAGTTTT | 79658 |
| rs528332398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147844988 | CCACAAGGCCCGGCA[C/T]GCTCTGATCCCCTGC | 79658 |
| rs528336997 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147838103 | TATTTAATAAAAAAT[G/T]TGTCCCAGCTCTTGG | 79658 |
| rs528354394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147936944 | CTGTCAGATCAGTGG[C/T]GACATTAGATTGTTA | 79658 |
| rs528358718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148026640 | GAACTAAAATGGATA[C/T]AGTATCTGGCTAGTT | 79658 |
| rs528365670 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147929325 | TAAATTTATGATGGT[C/G]AATATGTCCCTTTGA | 79658 |
| rs528372679 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147815614 | GTAATCCCAGCACTT[C/T]GGAGGGCCAAGGCAG | 79658 |
| rs528373196 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147873362 | TAAATAGAAGTGTGT[A/G]TACATGTTCACACCT | 79658 |
| rs528376696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148019720 | AGCTGAGCCGAGATC[A/G]CGCCATTGCACTCCA | 79658 |
| rs528397459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147763436 | CCTGCCTCAGCCTCT[C/T]GAGTAGCTGGGACTA | 79658 |
| rs528404540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147803255 | CTCAAGTGATTCACC[C/T]GCCTTGGCCTCCCAA | 79658 |
| rs528415937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148020382 | GCTGGTTTGCTGCAC[A/G]TATCAACCCATCACC | 79658 |
| rs528425150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147984038 | TGATTGTTTGGCTAC[A/G]TTTCTGGGTATTTTC | 79658 |
| rs528426496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147792288 | ATTTTCCTGATTGGA[A/G]TGAGGTTGAATATCT | 79658 |
| rs528426716 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148008423 | CAAGCAATTTTGGCC[C/T]GAAGGGGACATTTGG | 79658 |
| rs528434546 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889309 | TATTGGGTACCTTCT[A/T]TTTTTTTGAGATGGA | 79658 |
| rs528436316 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147976222 | TTGCCATTTAATGGG[A/G]AAAAGAAATCTCTTT | 79658 |
| rs528461337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147833805 | ATTAGATTCAATGAT[A/G]TATATATTAAGTTGG | 79658 |
| rs528462817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147745577 | GCTCACTGCAAGCCC[C/T]GCCTCCTGGGTTCAC | 79658 |
| rs528479277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147841043 | ACACTTGGACCCATC[A/G]TTCATATGCTGTTTG | 79658 |
| rs528486460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147798359 | TCATCCCTCCTTAGA[C/T]TATAAACTCTGAAGT | 79658 |
| rs528502274 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147914513 | TAGACATGAGCCACC[A/G]TGCTTGTCCCTGAGC | 79658 |
| rs528516681 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147894268 | ACTTCCTTACTAACC[A/T]TTGGTTATGTTACTC | 79658 |
| rs528530139 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148061060 | TTCCCTAAACAAACA[A/C]ACCCACCCACCCGCG | 79658 |
| rs528532740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147751928 | GTGTTGCTCTGCCAT[C/T]AGGTTGGAGTGCAGT | 79658 |
| rs528545496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147840423 | AGTTTTTTTTATTTC[C/T]TCCTCCTAAACCTTT | 79658 |
| rs528555687 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147847435 | CTAGTAATCTTCTTG[G/T]GCTACACCTTTCCAT | 79658 |
| rs528582631 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148014848 | AGTCTAAAAATGTTT[C/G]CTGAAATAAAACATA | 79658 |
| rs528583229 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147880827 | GTACTTTTAGGCTGA[C/T]GTGTATGGAATTGCA | 79658 |
| rs528589522 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147891124 | AGAAATTCTGCTCCT[A/G]GCTATACATTCAAGA | 79658 |
| rs528596076 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147797750 | CATTTTTTATTTGTC[A/T]CTTCGGTCTGATGTT | 79658 |
| rs528598839 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147864321 | CCCGCCTTTGAGAGC[C/T]GGGTTCTTGAGATGC | 79658 |
| rs528599350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147757592 | CCTTTACCAGCTTTC[C/T]ATCTGCTGTAGCATT | 79658 |
| rs528610310 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147854066 | TTCTTAGGTTCTTCT[C/T]TTCTACCATTTATAT | 79658 |
| rs528616647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147805150 | TGAGTTAATTTTTGT[A/G]TATGGAGTTAGGAAG | 79658 |
| rs528625425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147978360 | ACTTTTTAAATAATC[A/G]CCATTCTGACTGGTG | 79658 |
| rs528627709 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148063487 | GTTCAGTAGCAAGGA[C/T]GTTCTTTGGAGAATT | 79658 |
| rs528635251 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147867900 | AAGTTGAGAGTGAAT[A/C]CCTTTTGTGTAGATT | 79658 |
| rs528637585 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148040663 | CTGCAGGGTTTAAAT[A/G]TCTAGGTGGTTCTGT | 79658 |
| rs528638467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147898821 | TCTTTAGAGAGAAAG[A/G]GAGATGGGGTGGGGT | 79658 |
| rs528650291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147945526 | CGGATGACTATATTA[C/T]AGTGTTAATGTGAAA | 79658 |
| rs528671648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147804521 | CTGGGTATATACCCA[A/G]TAATGGGATTGCTGG | 79658 |
| rs528683473 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147841888 | CCTTGTTTTGGAAAT[C/T]TGCTTACCGATCTGA | 79658 |
| rs528692872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147764882 | CAGATGTGCTGAGGA[A/G]CTGTAAGTTTATTTT | 79658 |
| rs528714820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147853677 | ACAAATGTTTCCCTA[C/T]GTTCTTACATATTGG | 79658 |
| rs528723912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147861249 | CACAGGCACTGGCTC[C/T]GTGCAAGGCTGTGGC | 79658 |
| rs528731981 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147838859 | AACTAAATATCTTAA[A/G]TTTCTTAGTGTCCCT | 79658 |
| rs528739455 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147783313 | TAATTTATATAACAC[A/G]CATTAAATTATGTAT | 79658 |
| rs528769519 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148042593 | CACCTGTCTTTCGCT[C/G]CTGACACTGGTAACT | 79658 |
| rs528769563 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148034387 | CGATGGCGCGATCTT[C/G]GCTCACTGCAATCTC | 79658 |
| rs528773246 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147952249 | ATTTGAGTGGACGCA[A/G]GCTTTCATTTCTCTT | 79658 |
| rs528774581 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147866477 | TCCTGCAGAACATGC[C/T]ATATAAGCTGTCTAA | 79658 |
| rs528793599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147777534 | TGCTGGGATTACAGG[C/T]GTGAGCCACCACACC | 79658 |
| rs528801742 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARHGAP10 | GRCh38.p7 | 4:147730396 | ATTTTTGTTTACACC[C/T]CCTCTCTTCTTGTCT | 79658 |
| rs528812795 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147951678 | GGCTGGTCTTAAACT[C/T]GTCGTCTCAAGTGAT | 79658 |
| rs528815245 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147940121 | AAATGAAAAAAGAAT[G/T]CACCCCCTGGTTGAC | 79658 |
| rs528823005 | in-del | -/ATT | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147784002 | TAATTTATATAACAC[-/ATT]AAATTATTATATAAT | 79658 |
| rs528833933 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147861131 | ATGCCTGCCAAGGGC[A/G]AGCCAGGCACGGAGT | 79658 |
| rs528838318 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147806760 | AGGCTGGAGTGTGGG[G/T]ATGCCATCATAGCTC | 79658 |
| rs528871975 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147892864 | CTGGGGGTTAGAAGA[A/G]GGCAGGGAGTTGCTA | 79658 |
| rs528878258 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147813831 | TTAACAGCAGCTATA[C/T]AGCATATGTAGTCCT | 79658 |
| rs528884331 | in-del | -/A | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148016509 | CCTTGTCTCTGAAAG[-/A]AAAAAAAAAATTGAG | 79658 |
| rs528890708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147979788 | GGTTTTTGTGTAGGT[A/G]TGTGGCTATTGTAAA | 79658 |
| rs528894368 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147859311 | GAGTTTTGCTCTTGT[C/T]GTCCAGGCTGGAGTG | 79658 |
| rs528899501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148030556 | TGCTCTGAAAACTCT[A/G]TGGCCCATGATTAAA | 79658 |
| rs528900763 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147806064 | CATACTTTAAGCCTT[C/T]TGTTTATATTTATTT | 79658 |
| rs528901589 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148071187 | TGCACTTGCAAAGGC[C/G]TGGAGTTGCAGTTGG | 79658 |
| rs528918015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147855860 | TTTCCAGAAGAACAG[C/T]GTGTGGTCCCATGTG | 79658 |
| rs528925635 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148036576 | AAGGATGTGTTTGCC[C/T]CCCCTTCTGCCATGA | 79658 |
| rs528932606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147906256 | CATAGCAGCACTGTT[C/T]ACAACAGGCAAAAAG | 79658 |
| rs528933039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147767131 | GCTGGGATTACAGGT[A/G]TGAGCCACCGCGCCC | 79658 |
| rs528943893 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147899324 | GTGTGTGTGTGTGTG[C/T]ATGCGTGTGTGTGTG | 79658 |
| rs528950592 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147744676 | ACCTCAGGTTCTGGT[A/G]TGGGCTGGTGAGTGC | 79658 |
| rs528958112 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147995649 | AGAAAAAATAATAAC[C/T]TGGTATCAGTCAGAG | 79658 |
| rs528968550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148029997 | TGAGGCTCAGCATCC[C/T]CCCCCCCACCAACCC | 79658 |
| rs528972002 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147946946 | AAATAGACATTTTTT[C/G]TGGATGTACATTTTA | 79658 |
| rs528975478 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148007535 | ATTTTCTCCTTCAGC[A/G]ATTCATGAGTCAGCT | 79658 |
| rs528986317 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147758434 | GTGTAGTCACAGATT[A/C]GTGCAGCCATCACCA | 79658 |
| rs528988205 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147820734 | TAGCTGGTATTAAAG[A/G]CATGCACCACCATGT | 79658 |
| rs528996053 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147766561 | CTGTGTGTGGGTGTG[A/T]GTGGGTGTGTGTGTA | 79658 |
| rs528997842 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147773758 | AGAAGATTCTTGATT[A/C/T]TCTACCTTGGTTCTT | 79658 |
| rs529003499 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147863321 | TTTAACTACTCTAGG[G/T]GTCTCATGTGAGTGG | 79658 |
| rs529007734 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147801194 | CGTTCAGTAAAACAT[A/C]TCTCTCAGGGGTCTT | 79658 |
| rs529010717 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147971590 | TTTAAGAGGACATTT[C/T]GGGTATGGGAGACCA | 79658 |
| rs529014429 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147868940 | TGGGGGTTGGGGACC[C/T]CTGCTTGAGATTATA | 79658 |
| rs529029010 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147830131 | TTGCCTATGCAGACT[C/T]TTCAGGCTTTTGAGA | 79658 |
| rs529034825 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147938191 | ACATAGAGGAGAACA[A/G]CACATACTGAGGCCT | 79658 |
| rs529038622 | snp | G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | ARHGAP10 | GRCh38.p7 | 4:147731982 | GAGAAGGGGACGAGC[G/T]GGAGCGCGGGCCCGG | 79658 |
| rs529041112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147992981 | CCTCTGTCTTTCAGG[A/G]CATTATTAGTCATTA | 79658 |
| rs529042993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147970523 | CAGGCGAAAAATGGC[A/G]AGAAGGAAGTCATTT | 79658 |
| rs529052304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147868527 | GGGGGTGAGCCACCA[C/T]GCCTGGCTGATGTTG | 79658 |
| rs529053500 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148004401 | AAATAGTGATAGTGA[G/T]TGTGGCAGACTCACC | 79658 |
| rs529055528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147778805 | TTTAATAAGTGTTGA[A/G]TGAGTGGTACAGGGA | 79658 |
| rs529067218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147905827 | ATTACCTTGGGCAGT[A/G]TGGCCATTTTCACGA | 79658 |
| rs529071840 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147968680 | TTTTAGATTTTTTTT[C/T]CTTCAGTCACCTGTA | 79658 |
| rs529080900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148050956 | GGCAATGCCTTTACT[A/G]TGGTCTCAGGTCCTA | 79658 |
| rs529084487 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148035844 | TAAGGAAGATTTTCT[C/G]ATCAAAGAATCTGGA | 79658 |
| rs529089307 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147777301 | TCTCACTCTGTCACC[C/T]AGGCTGGAGTGCAGT | 79658 |
| rs529095237 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147827811 | TCACTTAATCTTTTT[G/T]TTTGTTTGTTTTTGA | 79658 |
| rs529105260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147992522 | AAGCCATTCTCTTGT[A/G]GCCCTCCTGAGAGGC | 79658 |
| rs529118112 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148044147 | GGAAGAGAGAACTCT[C/T]TTAATAGAATGTGAT | 79658 |
| rs529118298 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147917188 | TGGAAACTGTCTTCC[A/C]CAGCTGGTAATTGGG | 79658 |
| rs529136315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147960252 | TTTTTTTAATGATAT[A/G]ATATGATTTGGTTGT | 79658 |
| rs529144628 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147739508 | ACGTGAACTCAAAAT[G/T]AGGGTTTCTAGCGTC | 79658 |
| rs529145660 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148008848 | TGATATTAAGACATT[G/T]AATTAAAACATTGAA | 79658 |
| rs529146954 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147827239 | TTTAAATACCTTTGA[A/T]TGCTTACTAAAACAT | 79658 |
| rs529151538 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147916686 | GTAAAGATACGGGGT[C/G]CATCGCTGATGTTAT | 79658 |
| rs529157529 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147778364 | GTTTACAGTGTGCTA[A/C]AACTCTTTAACCTGG | 79658 |
| rs529161457 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147965823 | AAGTCCCAGCTTTCA[A/T]GAAGCTTACTTTCTA | 79658 |
| rs529168629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147786560 | GAAAATTCCATGAAA[C/T]GTTGAGTTTCAATGT | 79658 |
| rs529184199 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147738920 | GGGCTCAGTGGCTCA[A/C]GTCTGTAATCCTAGC | 79658 |
| rs529190288 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147962387 | TGCCAGCCACAGAGG[C/T]TAAGTGCTTTATGTA | 79658 |
| rs529195289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147954904 | TGTTTAATCTTTTCT[A/G]TGTATTTTGTGTGGA | 79658 |
| rs529196578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147874292 | AAGTGTCCAGGAACA[C/T]GGTGGTGCTGACTCG | 79658 |
| rs529217997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147880292 | AAAAAAAGAAAAACC[C/T]ATGTTCACTTCTATT | 79658 |
| rs529228881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147734441 | TCATGCTTTGAGAGT[A/G]ATTGGGAAGTGTCTT | 79658 |
| rs529228968 | snp | A/T | 8.61111e-05 | 0.00656111 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148064376 | TTCTCTCTGTTTTCC[A/T]CATTTTCATTGGTGT | 79658 |
| rs529247123 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147785966 | GAGTGTATTAACTCC[G/T]TTTACAGGTCAAACT | 79658 |
| rs529248484 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147961859 | CCTTCCTGATGACAT[A/C]GTACCTCCCTGGTCC | 79658 |
| rs529251439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147955159 | GTTAATAAAGTGATC[C/T]GTTTATGTATCTTTT | 79658 |
| rs529253393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148000398 | ACATAGTGTGCATGT[A/G]TCTTTATAGCAGCAT | 79658 |
| rs529259626 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147774728 | TGTGTTTCGTTTCTT[C/T]CTTGAACTTGCTTAA | 79658 |
| rs529260375 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147962400 | GGCTAAGTGCTTTAT[A/G]TATGTTACAGCATTG | 79658 |
| rs529268420 | in-del | -/TT | 0.021333 | 0.101051 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147864063 | ATGCCCAGATAAATA[-/TT]TTTAAGAGTAAAATT | 79658 |
| rs529285612 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148045998 | TGTAGAACATTGCTG[C/G]CTCTGCAGGGTTGCC | 79658 |
| rs529294219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147907602 | AAAAGCTAATGTTAT[C/T]TTGTGGTAACAGAGA | 79658 |
| rs529302210 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147815019 | CCAAGAAGCTTAAAA[G/T]ATTTGTTTGCCCCTA | 79658 |
| rs529309592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147961355 | TTTTGTGAAATTCCT[A/G]CCCCGGTCTTTTGCC | 79658 |
| rs529309776 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147967939 | CTAGGGAGGAAACGT[C/T]TCTTCTTTATTAAGA | 79658 |
| rs529312435 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147821544 | ACAGCACGATAAACA[G/T]GAATTAGAGGAAAAA | 79658 |
| rs529328470 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148045262 | CATCTCTAACTCCTG[A/C]TTGTCTGGATTCAGT | 79658 |
| rs529332493 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147919445 | CAAATATTTGCTAAT[A/T]ATACATACCGGCTCT | 79658 |
| rs529338179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148038251 | GAATGTCCTGGGTAA[C/T]ATTAGGAGGAAAGGC | 79658 |
| rs529352114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147739866 | TCAGCCTCCCAAGTA[A/G]CTGGGATTACAGGCG | 79658 |
| rs529361041 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147876166 | CCTTTTCCATTTGCC[A/C]TTATTTAATCTGGAA | 79658 |
| rs529372300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147780449 | GGAGCCCGGTCAGCA[A/G]GCTTGAAGGAAAGAG | 79658 |
| rs529372728 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147912219 | TTGGTAAATAGAGAT[C/T]CTGATATTCCAGCAA | 79658 |
| rs529376752 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147934103 | GCAAGTCTCAGGTTC[A/G]CTGCTGAGACCACTG | 79658 |
| rs529388191 | in-del | -/TTA | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147874159 | CCTTGGCAGCCCCTT[-/TTA]TTGTAGGGAGGAAAG | 79658 |
| rs529396189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148000152 | CATTGTTCAATTCCT[A/G]CCTATGAGTGAGAAC | 79658 |
| rs529407368 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148036380 | AGATCTCATCTTGAA[A/T]TGTAGTTCCTATAAT | 79658 |
| rs529429238 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148059215 | TAAGTTGGGAAGATA[G/T]CGAACAGATATTAGC | 79658 |
| rs529431808 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147909124 | CCCTCATCAGTTTAA[G/T]AATTTGCCAGATTAG | 79658 |
| rs529437713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148005771 | TTGTGTCTTGTCCTT[C/T]GATGACAAAAACGTG | 79658 |
| rs529449941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147746535 | CCTCCTGAGTAGCTC[A/G]CTTGCCACCACTCCC | 79658 |
| rs529455188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147788130 | AGCTCCTTTTAAAAA[A/G]TTTGATTTTTTTTTT | 79658 |
| rs529458212 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147765091 | CCAAGTTAATTTTTA[G/T]AATAGACTGTGGACT | 79658 |
| rs529464797 | in-del | -/CT | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147743066 | TTGGAGACAGTCTCA[-/CT]CTGTCACCCAGGCTG | 79658 |
| rs529466670 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147881244 | CACCACTGCACTCCA[G/T]CCTGGGCAACAGAGC | 79658 |
| rs529467812 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147794353 | TCAATCTTTGCAACA[C/T]AATGTTAATTCTCAC | 79658 |
| rs529467851 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147787680 | CGTGCTTCCCTGGCT[C/T]AGCCCTCACAACCAA | 79658 |
| rs529467935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148010030 | CTATAGTTAACTAAT[C/T]AAAACTTAATAGATG | 79658 |
| rs529470541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147761391 | CCTTTTAGTAGTAAT[C/T]GCTGTACTGACCACA | 79658 |
| rs529475270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147973456 | AGATATTTTGATAGA[A/G]GCATGCCATGGGTAA | 79658 |
| rs529509063 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147753971 | TTCATCTGCTACTAC[G/T]CGTTCTAAGAAAGAC | 79658 |
| rs529528506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147926607 | GGAGAGATGGCAGGA[A/G]TTATTTTTAAAGAGG | 79658 |
| rs529531337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147793715 | GAGTTAACATAATGC[A/G]GAGCCATGGATCCTC | 79658 |
| rs529536214 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147925727 | TCCTGCATAGTTCCA[C/T]GGATACTAGTAGAAG | 79658 |
| rs529544137 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148016305 | GACCAGGAGTTTGAG[A/G]TTAGCCTGGGTAACA | 79658 |
| rs529551053 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147753428 | GGCTCACTACAACCT[C/G]TGCCTCCTGGGTTCA | 79658 |
| rs529557198 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148052101 | GATTTGCCTAAAGTT[C/T]AGAAAAATAATCATT | 79658 |
| rs529560882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147940770 | TTTTAGGAAGCATGA[A/G]CCAAGTTGAATAAAA | 79658 |
| rs529565261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147848941 | TTTAATGACCAAATT[C/T]TTTCCTGAAGTCCTA | 79658 |
| rs529574179 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148023633 | CATGGTTCTTTTTTT[A/T]TTTTTAAAAGACAGC | 79658 |
| rs529575072 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148064860 | TCCCAGAGTTGCTAA[C/G]CAAGTCCTTTAAATG | 79658 |
| rs529603854 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148012458 | AGAGGCTGGTGCCTG[C/G]CACCAGTATGTGTGA | 79658 |
| rs529610889 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147789484 | TTTAGTAGAGATAGG[A/G]TTTCACTCTGTTGAC | 79658 |
| rs529613833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147760259 | AGGTTTACACACTCA[A/G]CTCATTAGATTTTCA | 79658 |
| rs529615008 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147883734 | AGTCTCACTTTTTTT[C/G]CCCAGGCTGGAGTGC | 79658 |
| rs529616271 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889527 | CTGGTCTTGAACTCC[G/T]GACCTCAGGTGATCT | 79658 |
| rs529650985 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147883113 | TAATAAATGAATTGA[A/C]GACCATTTATTGTAC | 79658 |
| rs529660482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147748952 | CAGCAGAGTGAGACC[C/T]TGTGTCTTAAAAAAA | 79658 |
| rs529663847 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147876825 | ATACAACTTGTCTCA[G/T]TTATCCATAAAACAG | 79658 |
| rs529678468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147742586 | CCTCCCGGGTTCAAG[C/T]GATTCTCCTGCCCCA | 79658 |
| rs529681878 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147969016 | CAGAGATCTTTTTGT[A/C]CACTTATAGTAATAC | 79658 |
| rs529696777 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147837926 | TAAACATAATAAAAT[A/T]GTTTCAGACAACTTG | 79658 |
| rs529699528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147929089 | TGTATTTCCAAGATA[C/T]GTTTGTTTTTTATTT | 79658 |
| rs529700009 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148072493 | GGAACTGTACTACTC[A/G]CAGTGATAGGTTTGC | 79658 |
| rs529707273 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148061615 | TTAGAAGAATAATGT[G/T]TTTTTTTTTTAAATG | 79658 |
| rs529715597 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147755127 | CTGCTTTAAAAACAT[C/T]CCAAACAATAAGGAT | 79658 |
| rs529736404 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147920780 | GGGAAGCATGTGATG[G/T]TAATTGAGGACTGTC | 79658 |
| rs529746485 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147975221 | TTTTGGTGTGACAGT[C/G]GAGGCCATTGTGGTG | 79658 |
| rs529761262 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148011754 | TATTTCCTAATTGTA[A/T]ATATAGCCATTTTCT | 79658 |
| rs529772738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147844098 | CATCTGGGATTTAAC[A/G]TGAGCCCTTAGTGTG | 79658 |
| rs529772923 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147850891 | TTTGTGGGTAGCTAC[A/C]GGAACCAGTACAGAT | 79658 |
| rs529775120 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148019491 | GCATGGTGGCTCACA[A/C]CTGTAATCCCAGCAC | 79658 |
| rs529776330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147928018 | AAGTCTAGGGCATCT[A/G]GTCTGAAGCTAAAAT | 79658 |
| rs529782108 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148018703 | CCCATTTTACTCTTT[C/G]TAAACAGATATAAGA | 79658 |
| rs529783391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148067007 | TCAGGACTTTGCTGG[C/T]TGGGGCACCCCGGGT | 79658 |
| rs529786235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147748143 | CTTGAGAAGTACAGT[C/T]ATGCTAAGACAATAA | 79658 |
| rs529795551 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147802403 | TCTCTAAAGCATAAT[A/G]TAGCTGAGCTATGAT | 79658 |
| rs529819155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147754718 | ACATAAAGCAAAATA[A/G]CAGGAAAAAGACAAA | 79658 |
| rs529821180 | in-del | -/CTTT | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148061198 | GTAGTCACATAGTTA[-/CTTT]ATCTTCTTCCTGTAA | 79658 |
| rs529825811 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147875564 | TCATTCATACACACG[C/T]ATACGTCCTCTCCCT | 79658 |
| rs529836075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147895309 | AATATTGCTAAGTGC[A/G]CTTATTCTGTTAGTT | 79658 |
| rs529855652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147801922 | TACAGAAAATGGAGC[C/T]GGAGTTGAACTCATC | 79658 |
| rs529855891 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | ARHGAP10 | GRCh38.p7 | 4:148072927 | GGAGCCTGGAGTATT[C/T]GGGGTGGGGCGTGTT | 79658 |
| rs529857616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148060993 | GCAGGCTTTTCTGTT[A/G]CGTATCTGTCATTAC | 79658 |
| rs529871671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147809350 | CATTCTGAAATAGCT[A/G]ACATGCATTTTTTTT | 79658 |
| rs529872091 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147902023 | TTGCTGCAGTGGTTC[G/T]TGATTGTCACTGAAT | 79658 |
| rs529872795 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147762085 | CAATCTCAGCTCATC[A/G]CAACCTCTGCCTCCT | 79658 |
| rs529888724 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147858201 | ATTTTCTCTTTGTTT[A/T]CTTCTAAATCCCCTG | 79658 |
| rs529896822 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147851808 | AATAAAAATATATTG[C/T]GGAAAGTGCTGTAAT | 79658 |
| rs529906169 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147777062 | GAAAATAACTGCTAT[C/G]CTGATAGCTGTTACA | 79658 |
| rs529918442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147808580 | GAGGAAAGAGTGGGA[A/G]CAGAGTAATGTGTTC | 79658 |
| rs529924330 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147894801 | TGCCTCTCATTTAAT[G/T]GTTTTGGCACCTTCT | 79658 |
| rs529937125 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148058784 | ACTGTCATAATTTCA[C/T]GTTTTGGGGTTTGGC | 79658 |
| rs529937384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147949187 | TTTTCTGAAACTGTT[A/G]TGTGCACTATTGTTA | 79658 |
| rs529938012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147768721 | TTTAAGTGCTTAAAA[A/G]TGGGGGCAAATTTTC | 79658 |
| rs529948782 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148025063 | TCCAGTCAAATTTAT[G/T]TAGTGGATTAACCTT | 79658 |
| rs529965131 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147877666 | GCATGTGAAGTTCCA[C/G]ATGCTAGAGGTCCCT | 79658 |
| rs529977711 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147988322 | AAACCAGAAGTAGCT[C/T]TCCTCTGAACTTCCA | 79658 |
| rs529980705 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147857361 | GAAATAAAAGTGTCT[A/C]TTCTATCCTAATGCT | 79658 |
| rs529985093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147995491 | GCCACATGTTACCGT[A/G]TATTATGTTTTCCTT | 79658 |
| rs529987266 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148072156 | GCTGTCTTCCTCCTC[C/T]GAGGCTCTGGGCTGC | 79658 |
| rs530006157 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147914099 | AGAGGTTGCAGTGAG[C/T]CGAGATCGTGTCACT | 79658 |
| rs530022253 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147872942 | GCTGAGAAGACTTAG[A/G]AGTGAGCACACTGTG | 79658 |
| rs530027288 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148032316 | TTATCTAATATTGGC[A/T]ATTTCAACTGTCCCC | 79658 |
| rs530059744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148068483 | ATAGATTCCTAGCAC[A/G]GGGGAATCTGAGAAA | 79658 |
| rs530062885 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148067812 | TGACCCAGAGTGTGG[C/T]TGGCACAGGGGTCTT | 79658 |
| rs530085170 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147870478 | AGCAAAACTTTATAA[A/T]CAGAAAAAGGTAAAA | 79658 |
| rs530093351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147984208 | TAGCTGCCTGGGGAA[C/T]GGGCAGAGGGAGGCA | 79658 |
| rs530094929 | in-del | -/GCAATCAC | 0.00636936 | 0.0560724 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147982430 | CTGGAGTGCAGTGGT[-/GCAATCAC]GCAATCACGGCTCAC | 79658 |
| rs530103731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889943 | GAAGCCCAGAGGTTG[C/T]CAGATCACAGCTGAT | 79658 |
| rs530119938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147976994 | TAATATTTATAATAA[C/T]GAGAACATGTTCATG | 79658 |
| rs530134774 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147984742 | CATTCAACGTCCAGG[A/C]CAAGAAGTGGCTTTT | 79658 |
| rs530146302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147769990 | TGCACATGTTCCAGA[C/T]AACAGCATAAGGACC | 79658 |
| rs530152065 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147815361 | AGCCAGAATGGTGGC[A/C]CTCCAGTGATGTCCT | 79658 |
| rs530161081 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147816943 | AAAGAATTTTGGTGC[A/G]TGTTTTGATGTGCAG | 79658 |
| rs530165208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147817870 | GGCAGAAGAGAATAG[A/G]GGGCATGGAGTTACA | 79658 |
| rs530167036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147810030 | ATTTTCTCTATAAGT[A/G]TGTCACATATAGTAT | 79658 |
| rs530177192 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148002601 | TCAGAGCCTGTTATT[C/G]GTCTATTCGGGGATT | 79658 |
| rs530188556 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147951697 | GTCTCAAGTGATCCT[A/C]CCACCTTGGCCTCCC | 79658 |
| rs530200410 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148001851 | ATATGCAGTCATGTC[A/G]TCTGCAAACAGGGAC | 79658 |
| rs530205485 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147852012 | TAAAATGAGACTTAC[A/G]ACACTTGTCTCAGGA | 79658 |
| rs530209479 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147770590 | CTGTATTTAACTTAT[A/T]GTCATGTGGTGTTAT | 79658 |
| rs530220339 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147777003 | TAAGTGGCTATATTC[A/T]TCACTGATCTGAGCA | 79658 |
| rs530227238 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147817226 | GCTTTCGTTGCTGGG[A/G]TGGGAAGTTGTAGGA | 79658 |
| rs530234685 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147849094 | CGTCATTGTAGGTCA[C/T]AGGGAGAAGCCCTTT | 79658 |
| rs530236258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147996515 | GACTGAGACTCCCTG[A/G]GGGACTGAAGGACCA | 79658 |
| rs530236883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147859615 | TTTGACAAACTGTGC[A/G]TTTGTTACGTGGCTT | 79658 |
| rs530238722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147943379 | ACAGCTTTGTTGCAT[A/G]GATTGGGGAAAAAAG | 79658 |
| rs530258826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147909044 | CTGAGTTCAGGTGCC[C/T]ATCACAAGTCTGGAC | 79658 |
| rs530260025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147990371 | GCTAAACTAAGGGCT[A/G]ACAGTCTTAGCTCAG | 79658 |
| rs530264413 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147860985 | ACGGAATTTTTAGGA[A/T]GTCTCTTTTCCAGCC | 79658 |
| rs530272523 | snp | C/T | 4.94466e-05 | 0.00497201 | synonymous-codon, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147864896 | CTATGAACTGTCTCT[C/T]GAGTATGTGTGTAAG | 79658 |
| rs530277855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147950185 | CTTGGGAGATTTGAA[A/G]GTTGGGTTGCTGTTC | 79658 |
| rs530280548 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147957195 | GGATTTGCACCTAAG[G/T]GCCGTTGTGGTTGGA | 79658 |
| rs530282064 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147996107 | TTAGAAGTAGGTGCA[A/G]GAGATGGTTTGGGCA | 79658 |
| rs530304278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147831196 | GGTTAGATCTGTCTG[A/G]ACGTTGGATACACTC | 79658 |
| rs530305506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147789567 | GTGAGCCACCATGCC[C/T]GGCCCACATGTTTTA | 79658 |
| rs530328592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147921370 | TCTACATCTGTTGAA[C/T]CAGAATTGTTGACGA | 79658 |
| rs530331209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147914187 | TTGAGGTATAATTTG[C/T]AGTCAGTACAATTCA | 79658 |
| rs530354784 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147877234 | GGGCAGTTTTTTTTT[C/T]CTTAGAGTTAAATAA | 79658 |
| rs530377504 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARHGAP10 | GRCh38.p7 | 4:147731210 | ATGCCTAACTTTTTT[G/T]GGGACACACTGGAGT | 79658 |
| rs530378738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147963062 | AGAAAAATATCAGGC[A/G]TACCTTCCCCAAATA | 79658 |
| rs530380663 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147767106 | TCCACCCACTTTGGC[C/T]GCCCAAAGTGCTGGG | 79658 |
| rs530383561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147860935 | TAGTTACAACTTGGA[C/T]GTCCATGGCATTCTT | 79658 |
| rs530390792 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147998459 | TGAAACTGGTCTACA[A/C]CATAGTGAAGGAAAA | 79658 |
| rs530394413 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147823607 | TACAAAAATACAAAA[A/G]CTAGCCAGGCATGGT | 79658 |
| rs530407910 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147924559 | GTAGTGCTGAAGGTG[-/T]TTTTTAGAACAGAAG | 79658 |
| rs530411023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147776014 | TTTAAATCCAGGCTC[C/T]GAAAAGTTAGCTCCA | 79658 |
| rs530413518 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147912456 | TGAGGTGGAAGAATC[A/G]CTTGAACCCAGGAGG | 79658 |
| rs530413936 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147780271 | TGTCTGGATCAGGGC[C/T]GAGGCTCAGCATGCC | 79658 |
| rs530415573 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147858970 | CAGAATATAATCAGA[A/G]TGTGTCCACTTCTCA | 79658 |
| rs530417768 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147811389 | TAGGGAGTTTGGTCT[A/C]CCTGAGGCATGTGAT | 79658 |
| rs530443621 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147791551 | GCGCGCGTGCGTGCG[C/T]GCGTGTATATATATA | 79658 |
| rs530450670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147771768 | AATTCTCATCTTCCT[C/T]GCCTCCACTCTTGCA | 79658 |
| rs530453629 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148001390 | TAGGATTGTCTTGGC[A/G]ATGCGGGCCCTTTTT | 79658 |
| rs530458668 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147857286 | GAATTAATTTTTAAC[A/G]TTGCTAAGTCTGAAG | 79658 |
| rs530463357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147738740 | GTTCTGCACCCTAGA[C/T]CAGGTATCTAACCTT | 79658 |
| rs530472585 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148059295 | AGGAACAGTTGACTT[A/C]TTCCTCCATTTTCGC | 79658 |
| rs530476709 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147973934 | TTTCTTTATCCATTT[G/T]TCTGTTGATAGACAC | 79658 |
| rs530483187 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147898459 | AAATAATTTTTATGA[-/T]TTTTTTTTTTGCCTT | 79658 |
| rs530490747 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147755471 | GAGGTTGCGGTGAGC[C/T]GAGATCACGCCATTG | 79658 |
| rs530492849 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147833536 | GACTAATTCATGTGG[A/G]AAAAACCAGATTTTG | 79658 |
| rs530496180 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147826427 | GTATAAGGCCATGAA[A/C]CTTAGGAGTGGTGTG | 79658 |
| rs530514047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147777644 | TCAGATCTCTTAACA[C/T]TGGATCACACTGACT | 79658 |
| rs530515557 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147904917 | TGACTTTTTAATGAT[C/T]GCCATTCTAACTGGT | 79658 |
| rs530517952 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147811768 | TGGTCGCTAGCCACT[G/T]GCAGAGTGCAATTAA | 79658 |
| rs530519422 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147945572 | ACTTTTTAAGTCTCT[A/G]TGTAGTTATTTTCTG | 79658 |
| rs530525884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147819393 | ACAAGATCCTGTTGC[A/G]ATCTGGCAAAGCAAA | 79658 |
| rs530540452 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147826867 | TGATACTCATTCCAA[G/T]TCTGCCTCTTTCCCT | 79658 |
| rs530550235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148035096 | AACCTGATGCCTATT[A/G]GCTGTTGCTATAACT | 79658 |
| rs530553462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147873047 | TGTTAAGGCTGAACT[A/G]TATGTACATCTATTT | 79658 |
| rs530555815 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147958129 | ACCACAGGCAGGCAT[C/G]TAGCTGGATGTCTTA | 79658 |
| rs530578018 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147990761 | GAACAACAGACGCCG[A/G]GGTCTACTTGAGGGA | 79658 |
| rs530581514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148041990 | CTGTGCGTGACTTTC[A/G]GATCAATAAAACTAT | 79658 |
| rs530582452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147737457 | ACTGCGCCTGGCCTT[A/G]ATGGCCTAATTTTGA | 79658 |
| rs530592872 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147892168 | GAATTCACTTATTTA[C/T]ATTTTTATGTTGAGG | 79658 |
| rs530609441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147970843 | CTGTAATCTCAGCAC[C/T]TCGGGAGGCCAAGGC | 79658 |
| rs530620141 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147886572 | CTCATCACAGTCCCT[G/T]TTTAATACCCTTCAC | 79658 |
| rs530620858 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147744455 | ACAGTAGGAAGTGAT[C/T]GAAAAGTTTTGTGTA | 79658 |
| rs530624492 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147829057 | CTAATTTTTTTGTAT[-/T]TTTTTTTTTTTTGAG | 79658 |
| rs530628328 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147855048 | ATTAAATCAAATAAG[A/G]TGGTAAAAATGTTTT | 79658 |
| rs530636107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148056998 | CATGACTCTCTTCAC[A/G]TTAGCTGAGGGAGTT | 79658 |
| rs530657260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147997541 | GAATGAAAGGAGAAA[A/G]ACAGATGAGAAGATG | 79658 |
| rs530659855 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147923135 | GTTGGAATTGGTACT[A/T]TCACATAACATGTAG | 79658 |
| rs530669393 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147977380 | ATATATGGGCTTGGT[G/T]TTTTGCCTTGAGCTA | 79658 |
| rs530674908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148063619 | TAAAGCACATTCTTC[A/G]TTTTAAAAGTAGGCA | 79658 |
| rs530676436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147838939 | AATGTGATTAGGGCT[A/G]TTTTAGGCTAAGATT | 79658 |
| rs530691974 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147791604 | GTTTTTTGTTTTTCC[G/T]CCCTGCGGGGCATGG | 79658 |
| rs530691981 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147784267 | AAATTGTGTATTATA[G/T]AATTTACATAACATT | 79658 |
| rs530702608 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148021157 | CGGGTTGGACCCAGC[C/G]CTGAGATTTGGACTG | 79658 |
| rs530734528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147845577 | TGACTTGGAATCCCT[A/G]TTCCTATCTTCTGTG | 79658 |
| rs530737917 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147758187 | AGAATTGCTTGAACC[A/C]GGGACGTGGAGGTTG | 79658 |
| rs530756012 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147797165 | CTCTAGTGGCCTTTT[A/C]CTTTCATTTAATTCT | 79658 |
| rs530778177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147793528 | GGACCTGGGATCTCC[C/T]CGCATAGCTATTTAG | 79658 |
| rs530781381 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147751189 | ACCTCAAAACCAAAA[A/C]CAAAAAAAACAAACA | 79658 |
| rs530785570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147970353 | GGACAAGATGAAAAC[A/G]AGAGAGGGAGTAAGG | 79658 |
| rs530786643 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147921019 | AGAAACAGGCATTCA[A/G]AAAGTAAATATGAAA | 79658 |
| rs530787153 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889451 | ATTACAGGCATACAC[C/T]GCCACGCCCGGCTAA | 79658 |
| rs530788762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147880979 | GTTAATCTACCTTTG[A/G]AAATTAACATTTGGC | 79658 |
| rs530796637 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147827891 | GCTCACTGCAGCCTC[C/T]GCCTCCCAGGTTCAA | 79658 |
| rs530804321 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147790962 | CATTCTATAAGTAAC[C/G]ACTATTGTGGATTTG | 79658 |
| rs530812482 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147922515 | TAAAACGGTGAAACC[C/T]CGTCTCTACTAAAAC | 79658 |
| rs530816994 | in-del | -/AA | 0.10237 | 0.201756 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148061466 | CGTTCCTTTTCTGCT[-/AA]AAAAAAAAATGGAGT | 79658 |
| rs530817011 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147764805 | CTCCCAAAGCGCTGG[G/T]ATTAGAGGCATGAGC | 79658 |
| rs530818872 | snp | C/G/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148030645 | GTTCATTTTTACTTA[C/G/T]TGAATTCTTACCAGC | 79658 |
| rs530827047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147886690 | ATTTCTACTGTATTC[A/G]TGGGATCACTTCAAA | 79658 |
| rs530855060 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147785339 | GCTTCTTTCTGTTCT[C/T]TGGTCCCGGATTTGA | 79658 |
| rs530868922 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148018114 | TGGATTGTCAGACTT[C/G]AGTTTTTCTTATGTT | 79658 |
| rs530896540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148015495 | AACAAACGTGAAACT[A/G]TAGAATATTTCCAGC | 79658 |
| rs530905519 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147839424 | AGTGTTCTGGGGAAC[C/G]GATGTAAAATTCCTT | 79658 |
| rs530906348 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148050595 | AGCCAGGATGGTCTC[A/G/T]ATCTCCTGACCTCGT | 79658 |
| rs530922328 | snp | C/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147972895 | AAGTAGCTGGGATTA[C/T]AGGCATGTGCCACCA | 79658 |
| rs530934592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147745928 | AGTAGCTGGGATTAC[C/T]GGTGTGCACCACCAC | 79658 |
| rs530935640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147759093 | TAGAATAAGTAACAC[A/G]TGGTAGATACAAAGA | 79658 |
| rs530941517 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147862198 | CAGGGGCGCTGGCAT[A/G]TCAGAACCACCCTGT | 79658 |
| rs530944269 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148051019 | AGGACCCCAGTAGAT[C/G]TGTTGAACAAAAATG | 79658 |
| rs530965447 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148069967 | TGAAGAACAATGTCA[A/G]AGTCAAGGTCAGTGA | 79658 |
| rs530969263 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147925490 | ACATGAGTGATGAGC[C/T]TGAAAATTTATTTAG | 79658 |
| rs530972875 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147834540 | CATCTTTTAAGGCCC[C/T]ACCTCTCAATAATGC | 79658 |
| rs530988267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147751995 | GGTTCAAGCAATTCT[C/T]CTGCCTCAGCCTCCT | 79658 |
| rs530990663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147985995 | GGGGTGTCCTTTGCT[A/G]TTGAAGTGGATTTCC | 79658 |
| rs530990867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147885925 | CGAGATCTATAATGC[C/T]TCCAAATGCAAAAAT | 79658 |
| rs530997734 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147863954 | TGAGTGTGAGGTGGC[A/T]TCTCCTTGTGAGTTT | 79658 |
| rs531013282 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147793031 | TAGTCCCAGCTACTC[C/T]GGAGGCTGAGGCAGG | 79658 |
| rs531032816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148064013 | CCTGTGGAGTGTGGC[C/T]GTGCCGCCTCCTTCT | 79658 |
| rs531036390 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147885052 | TAGATTTCTGGGGAT[A/G]AACTGGATGTTGCAG | 79658 |
| rs531042386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147932518 | GGGACATGGATGGAG[C/T]TGGAGCCCATTTTTC | 79658 |
| rs531049382 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147758219 | GGTGAGCCAAGATTG[C/T]GCCATTGCACTGCAG | 79658 |
| rs531085909 | in-del | -/TACT | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147982867 | CTCGTATTTCTCAAA[-/TACT]TACTTACTTTCTTTT | 79658 |
| rs531090430 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147861636 | GAGACCTGAAGTGAG[A/T]AGCCTTTTTCTGCAG | 79658 |
| rs531111233 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147835627 | GATCTGCCCGCCTTG[A/G]CCTCCCAAAGTGCTG | 79658 |
| rs531119593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147891883 | TATCACCCTTCCCCC[A/G]CCCCAACAATTGTGT | 79658 |
| rs531133487 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147945759 | ATGCAGGATTTTTTT[C/G]CTCCTTGGTTCAGCT | 79658 |
| rs531147445 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147985410 | GGCTGGGCACCCAGC[A/T]GGGACACATGCAAAC | 79658 |
| rs531148829 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147813152 | AGCCTTTTTTTTTTT[A/T]AAATAAAAGAATTGT | 79658 |
| rs531150715 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147805250 | CTTTCCCCATTGTTT[G/T]TTTTTGTTGACTTTG | 79658 |
| rs531169148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148064908 | CTGAGTCAACAGAGG[A/G]TACTACTGTCCTTAA | 79658 |
| rs531173702 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147741112 | TTTTCCTACAAGTGA[C/T]ATTTAAAAGGACTTT | 79658 |
| rs531176437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147931720 | TTTTGGAATTCAGAC[C/T]TTTTTAATTAAAAAA | 79658 |
| rs531183440 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147861837 | TCTGGGCTCAGAAGG[A/G]AGGAAGTGTGCTGAT | 79658 |
| rs531189423 | in-del | -/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147841151 | TACCTGGTCTTTTAT[-/G]GGAAAAAGTTGGCTG | 79658 |
| rs531210445 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148059439 | TCAAAAATCCGTAGT[A/T]AAAGGGACAACAAGA | 79658 |
| rs531212278 | in-del | -/T/TT | 0.201418 | 0.245234 | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147781681 | TTTTCTTTTCTTTTC[-/T/TT]TTTTTTTTTTTTTTT | 79658 |
| rs531216708 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147938576 | CAGCATAGAGACTCC[G/T]AGAGGTTTCCTCTCT | 79658 |
| rs531229332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147807577 | ATAATGGAAAAACAT[C/T]TGACTACCTAAAAAT | 79658 |
| rs531245300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148024117 | GGGAGCTGTGCACAC[A/G]CCTCCCATTGCTAAT | 79658 |
| rs531246552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148017062 | CGGGAGGCTGAGGCA[A/G]GAGAATCGCCTTTTA | 79658 |
| rs531253659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147934325 | GCACTCTCAAAGTGA[C/T]CCTCCCAGGTCTTGG | 79658 |
| rs531261090 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147767934 | GCAAAGATATGAGAT[C/G/T]ATCAAATTATGAAAT | 79658 |
| rs531268009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147812403 | AGCTTGACCTTGCTT[A/G]TGAGGAATACTTCAC | 79658 |
| rs531269931 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148030656 | CTTACTGAATTCTTA[C/T]CAGCTGTTGAGGAAA | 79658 |
| rs531286413 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148069338 | AGGATCCCCCTTGGT[C/T]GCCTCTGTAAAGCAG | 79658 |
| rs531288210 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148016345 | CTGTCTCTACAAAAA[C/T]GTTAAAAATTACTTG | 79658 |
| rs531294425 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147952275 | CTCTTGGATAAATCC[C/G]AGGAGTGGAATATTT | 79658 |
| rs531308131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148023806 | GCACAGTTCACCATC[A/G]CTCTGGGGTTTATGG | 79658 |
| rs531308719 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147754017 | ACTTTGATACCCCTC[A/G]CCTTGCCTGTGTTCC | 79658 |
| rs531314768 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147887217 | TCCCGCTCTAGACAC[C/G]CACCTCCACCCTCAG | 79658 |
| rs531321757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147774549 | AGGTTTCTTTATTCT[A/G]TAACATATTTACTTA | 79658 |
| rs531330199 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147967936 | AATCTAGGGAGGAAA[C/T]GTCTCTTCTTTATTA | 79658 |
| rs531340101 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147814729 | ATGCTTTGAAATAGT[G/T]TTCTCATCTGTATAT | 79658 |
| rs531342142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147806928 | CTGCCCCTGCCACCC[A/G]GTTCTAAGAAGTAGA | 79658 |
| rs531351883 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147973549 | AAGCAATCCAGTTAT[A/G]CTCTTTTAGTTATTT | 79658 |
| rs531357932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147893869 | TTCTAGTATATAGGT[C/T]TCTGTGTTTTTCATA | 79658 |
| rs531360264 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147995306 | TATACACCATTCATA[C/T]ACGATTTAAGGGCAC | 79658 |
| rs531368191 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147849935 | GCTATCACAGTGAGA[A/G/T]GTGAAGCCAGCTGGG | 79658 |
| rs531370930 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147993047 | TACCTTCTTTCTAAT[A/G]TCTTACCTATGCATA | 79658 |
| rs531382671 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147880639 | ATGTTAAAATGTTCA[A/G]TAAGTGTGTACTCAC | 79658 |
| rs531388173 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147760336 | TATAGAAATGTTTAC[A/G]GATGACTATGTCAAT | 79658 |
| rs531388435 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147831478 | GTATTTTATATGGCA[C/T]GTGAAGCTTGTTTTA | 79658 |
| rs531394218 | snp | A/G | 1.64974e-05 | 0.00287201 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147906736 | TAAGAATAATCAATG[A/G]TTGAGTTTTATTTCA | 79658 |
| rs531397692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148036710 | AAGAATGGACTGATA[C/T]AAGTTGACTAGCATA | 79658 |
| rs531402209 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147814111 | CTCAGATCTAGGGCA[C/T]GGACTCCTTAGGGCA | 79658 |
| rs531409987 | in-del | -/GTGGTAGCAC | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147792055 | GAGTAGAATTGCTGT[-/GTGGTAGCAC]GTGAGCGTCTTTCAC | 79658 |
| rs531421370 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147940943 | TCCATAAGCTGTTTT[C/T]ATTTTCTGCCTCTCT | 79658 |
| rs531434031 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911968 | GGATTGTGTTCTTAG[A/T]TTCTCAAGTAATTTA | 79658 |
| rs531439224 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147855934 | GTTTAATCTCTTTGC[C/G]TAACAGGAAGGAAAT | 79658 |
| rs531459581 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147947729 | TCTTTTTAACCATAC[A/G]TAGGGTTGTTTTTCA | 79658 |
| rs531462292 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148044192 | GACAATTTGTGCTGT[C/G]TCAGTCTGCTTGGGA | 79658 |
| rs531473569 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147987449 | CTGGGTCCCTCCTCA[C/G]TCTGTAGTGCCCTGT | 79658 |
| rs531475406 | in-del | -/C | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148006287 | TTTCCTGTCCAGGCA[-/C]TGGACATGTGAAGAA | 79658 |
| rs531481623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148071244 | TGACATGCATGATGT[A/G]CCAGTGGAGTGTGAA | 79658 |
| rs531493836 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147779828 | TTCTAAATATGTAAT[C/T]TGTTGACCCTGAAAT | 79658 |
| rs531496464 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147954564 | GTTACAGGATTGTAA[C/G]CTTTTAAAAGTTCTT | 79658 |
| rs531507787 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911524 | CCCACCATCACGCCC[A/G]GCTAATTTATTGTAT | 79658 |
| rs531507966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147787372 | TAGGAAACACATGAA[C/T]ACAACATCAGCAGGG | 79658 |
| rs531536083 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147986961 | GCTTTAGGTAAAAAC[C/G]TTTTGTCTTCATTGT | 79658 |
| rs531540322 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147868661 | GTTTTAAGGAAGACA[A/G]TTCTATAGATGCAGT | 79658 |
| rs531543567 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147820868 | AGTGCTGGGATGACA[G/T]GCGTGAACCACCACA | 79658 |
| rs531559142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147773856 | GAAACCCCTTTATAG[A/G]ATTATTTCCTTGTCT | 79658 |
| rs531563039 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148037464 | GCAGGGAGTAAGTAG[G/T]ATACTTTGACCTGTA | 79658 |
| rs531565258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147864288 | TTCTGAGGGCCGCAG[A/G]TGGGCGTCCAGCCCT | 79658 |
| rs531576849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147732852 | CCGAGGCATCTGTTT[A/G]CCTAGTTTTGTTTTG | 79658 |
| rs531590347 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147792017 | ATGATGTGTATGTGC[A/G]TTTCTCTGGGGACAT | 79658 |
| rs531601436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147960340 | GCTGTCTTAGTGTCC[C/T]CAGTTGTAAAATATC | 79658 |
| rs531606574 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147816248 | CTCCAGTGTGGAGCT[G/T]CCTGTGGGATTCTCT | 79658 |
| rs531606936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147828626 | CTGGGCTGAGTTGAA[A/G]GATGAGCCTTAGCTA | 79658 |
| rs531610766 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147995951 | CTCCATCTCCTGACC[C/T]CGTGATCCGCCTGCC | 79658 |
| rs531611650 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147739880 | AGCTGGGATTACAGG[C/T]GCCTGCCACCACACC | 79658 |
| rs531613516 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147732095 | CCGGGATTGGGGCGC[C/T]GCAGCTAGCGCTGGT | 79658 |
| rs531618344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147823336 | AACAGAGGACAGCTG[A/G]GCAATGTTAGTGCCT | 79658 |
| rs531627799 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147984960 | GGCAGGTCCGAGCAT[C/G/T]AGCTTTGAGGGGTGG | 79658 |
| rs531630625 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147869192 | GAAGCTCTTCTGAGC[G/T]CAGGGCCCTGTGGAC | 79658 |
| rs531632595 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147936457 | CCTCAGCCTCCCGAG[C/T]AGCTGGGACTACAGG | 79658 |
| rs531634906 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147735514 | GGAATGGTGGTTTTT[C/T]AGGGAGTAGTAGACT | 79658 |
| rs531635697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147954083 | GTGTCTTAAACCCTT[C/T]TTATTTTTTGAGATT | 79658 |
| rs531649037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148046699 | ACATTCCTCGCTGTG[C/T]ATTATCTGTGGTTTA | 79658 |
| rs531663413 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147775726 | GAGTCTTAGTTTCCT[C/T]CTCCCTAGGCATGGG | 79658 |
| rs531665483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147830491 | TGCCACTTTTTTTTT[A/G]AATGGTCAAAACCAC | 79658 |
| rs531667366 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147803783 | CTTTTCTGTGGCTGA[A/G]TAGTATTCCATTATA | 79658 |
| rs531679654 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147913962 | GTTCGAGACCATCCT[C/G]GCGAACATGGTGAAA | 79658 |
| rs531688738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147948839 | GGCATGGTGGTGGGC[A/G]CCTGTAGTCGCAGCT | 79658 |
| rs531688980 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147955797 | TGGAGGTGGCTTCAC[A/G]TAGACAGATACTCGG | 79658 |
| rs531689372 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147977636 | AGTTGAAATCTCAGC[A/T]CCACTCAATTGTGTG | 79658 |
| rs531693144 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148014168 | AATGTTAGTCTAGGC[A/G]TTTATTACTGAAATG | 79658 |
| rs531695498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147995556 | TATTATCTAAAACAG[A/G]TATCTCAAACATGTT | 79658 |
| rs531708077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147871237 | TGCTGGGATTATAGG[C/T]GTGAGCCACCACGTC | 79658 |
| rs531714357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147734682 | GGTCTTATTCTTTTG[C/T]GTCCAACTTCCCCTG | 79658 |
| rs531720683 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147793511 | CCTTGAAAGGAGGAG[C/T]TGGACCTGGGATCTC | 79658 |
| rs531726386 | snp | A/G/T | 3.30389e-05 | 0.0040643 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147955290 | TTGGATTTATTTGAT[A/G/T]ATTCTGAGCTGTTCT | 79658 |
| rs531731827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147902117 | AACAGCTTTCATACT[C/T]ATCATTTTGTTGCCC | 79658 |
| rs531733242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147815720 | AAATAGGCGATAGGC[A/G]TGGTGGTGGTGGTTT | 79658 |
| rs531733419 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147989182 | TTTATTAGGGAGTTT[C/G]AAAAGGGGAGGGAGT | 79658 |
| rs531734223 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147851220 | CTCATTACCAGACCT[C/G]TACTCCAAATTTCTT | 79658 |
| rs531740580 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147768025 | TTCAGGCATGAAACA[C/T]ATATTTGTTAATGGA | 79658 |
| rs531741762 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147772658 | GAGTTTAAAATCCTA[C/G]GGTATAAACGGCCAC | 79658 |
| rs531756888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148032460 | ATCAGTTATTAGCAA[A/G]TCTGTACCTTGTGAA | 79658 |
| rs531759419 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148008604 | ATAGTGCTGAGATTG[A/T]GAAGCCGTCAGCAGA | 79658 |
| rs531760116 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147933854 | GAGAGCCAGGCTCTT[G/T]GGGTGTATGTCTCAT | 79658 |
| rs531766473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148052818 | GAACAGGGGCCAAAT[A/G]AACAGGAGGAACATG | 79658 |
| rs531773657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147741666 | CTTTTGTATTGAGAA[A/G]GCCTTGATATTGTTC | 79658 |
| rs531801657 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148046126 | GTGAAAGCAAGAAGA[C/G]CAATAGAGGGAAATA | 79658 |
| rs531803898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148053761 | CTATGCCGACTGCCT[A/G]GCCCCTTACATGCTT | 79658 |
| rs531808698 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147771432 | GTAAATAGGGTATCT[A/G]TCACCTGAGGCATTT | 79658 |
| rs531826072 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147775460 | CAGGGGCCAGTGACA[G/T]TTAAGACTCTTCCTC | 79658 |
| rs531826193 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147958532 | AACATATCTGGGAAG[A/C]AAGACAAAAATCATG | 79658 |
| rs531828620 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147836420 | TTATTCTTGGATTAT[C/G]TGTATGAAAGCAGAA | 79658 |
| rs531834764 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147769504 | ATTGCTTCTCTTTAT[G/T]TAATAAATTCCTTGT | 79658 |
| rs531834949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147781674 | TTTCATTTTTTTCTT[C/T]TCTTTTCTTTTTTTT | 79658 |
| rs531838663 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147836021 | TGTTTTATGATTCTC[A/T]TTTTTTCCTAAGTGT | 79658 |
| rs531841123 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148000452 | ACCCAGTAATGGGAT[G/T]GCTGGGTCATATGGT | 79658 |
| rs531843485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147781184 | TAACATGGTGAAACC[C/T]CGTCTCTACTAAAAA | 79658 |
| rs531856413 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147927404 | TTGCTGCAACACCTC[A/G]TGAGGTCTCTTCATA | 79658 |
| rs531868292 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148000871 | TTTTCTCCCATTCTT[C/T]AGGTTGCCTGTTCAC | 79658 |
| rs531874225 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147876654 | CTTGAGAATGTTAGA[A/C]TTATTTGTATTATAT | 79658 |
| rs531887269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148010173 | AAGTAGGTGAGGAAT[A/G]TAGTGATTAAATGGT | 79658 |
| rs531892739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147934768 | GATCCAAGGAGGTCA[A/G]GGCTGCAGAGAGCTG | 79658 |
| rs531902563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148005844 | GTATTATGTTAATTG[C/T]GAAGCATTTACATGT | 79658 |
| rs531922030 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147878281 | TTTTGTATTTTAGTA[A/G]AGACAGGGTTTCACA | 79658 |
| rs531924960 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147968254 | GGCCTGCCTCTCTCC[C/G]GCTGTCTCAAGCCCC | 79658 |
| rs531928866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147913325 | TTCCTTTTTATTTAC[A/G]TATTTCTTTCCTATA | 79658 |
| rs531930253 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147850410 | CACTCTTTGGGTCCA[C/T]ACTACCTTTATGAGC | 79658 |
| rs531948528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147882394 | TTTGAACCCAGGAGG[C/T]GGAGGCTGCAGTGAG | 79658 |
| rs531955039 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147877859 | ACAGGCATGAGCCAC[A/G]AGGCCCAGCCATTCT | 79658 |
| rs531957439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147887718 | AATACAAAAATTAGC[C/T]GGGTGTGGTGGCGGG | 79658 |
| rs531966249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147919537 | CAAACTTTGCTGCAC[A/G]TTGAAATTACCTGGG | 79658 |
| rs531987897 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147884336 | CGAAGGATAATACCT[C/G]TAGGGAGACTCTTGG | 79658 |
| rs531997818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147974391 | CCCCCACTTCCTAAG[A/G]GCCCTTGAAGATTCT | 79658 |
| rs532006052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147915401 | TTCTTTTTTTCTGAG[C/T]TTCTTAAGTAGAACT | 79658 |
| rs532007739 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148017707 | ATGTAAAGGAATTCA[A/G]GGAGAGGAAGTGTGA | 79658 |
| rs532018400 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147747217 | TCACCGGAGTCATGC[C/T]GATTCTCTTTGGATG | 79658 |
| rs532019306 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147788250 | AGGAGTTTGAGACCA[C/G]CCTGACCAACATGGT | 79658 |
| rs532027573 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147907272 | ACCAAGATTCAGTCT[G/T]TTGGCCACTATTGAA | 79658 |
| rs532034714 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147976887 | AAAGTGTGCATAGAT[G/T]TATTCTGTGTTGTCT | 79658 |
| rs532040322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147963802 | TGGTGGTTGCTGGCC[A/G]TCCTTAGTATCCCTT | 79658 |
| rs532043012 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147749801 | CTGAGACGGTCAAAC[G/T]AAATATTTGTTATGT | 79658 |
| rs532043673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148010791 | GAATCTGCATTTGAA[C/T]AAGAACACCAGGTGA | 79658 |
| rs532049719 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147842905 | ATAAACTCCTCCTCA[C/G]CTATCTCAAAAGGAC | 79658 |
| rs532066279 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148066432 | CCTAAAGCCAATGCA[G/T]ATCTGCCAGTTTGGA | 79658 |
| rs532072373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147794388 | TTCCTATGAAGAGGA[C/T]CCTATAATTATCTCC | 79658 |
| rs532072393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148060311 | CCCAAAGTTTGGAAG[A/G]TAAGAGATGGTTACA | 79658 |
| rs532093993 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147744230 | CCAAAAGGAGGGATC[A/G]GAGCTTTCCCTGCTG | 79658 |
| rs532098133 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147790691 | TGGTGGCCAATGTTA[A/C]AGTTATATGCTGTTA | 79658 |
| rs532104474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147736782 | AGAAACTATAAGTCC[A/G]TTATGATAAACCCAT | 79658 |
| rs532120580 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148047388 | TTAGAGATGTGAGAA[C/T]GCATGCTGATGGACA | 79658 |
| rs532120732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147824813 | TGGAGTTTACGCTTT[C/T]GTGTAAGATTTGGGT | 79658 |
| rs532154165 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147755766 | AAGCTGGACTATCAC[A/G]AAAGAAGGTGGGGTG | 79658 |
| rs532154525 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147983334 | GGGACTACAGGCGCC[C/T]GCCACCACGCCCAGC | 79658 |
| rs532169328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147951628 | TTTTCAAAACATTAA[A/G]AAAAAATAGAAACAG | 79658 |
| rs532177770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147922297 | GGTTGCCTTGCCTTT[A/G]AGTGATAAGGACCTA | 79658 |
| rs532178034 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147922368 | TGGAAGGATTCTTAA[C/G]CTCTCAGACCCTTAG | 79658 |
| rs532182465 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147816828 | AGAGGAATTTCATTT[C/T]ACTTCCAAGTTACTT | 79658 |
| rs532189470 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147969820 | CTAAGCAGAGGTCTT[G/T]CGGTTTTCCTTCTCT | 79658 |
| rs532192417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889240 | TAAACCTAACTTGTT[A/G]TGGAGTTTGTGGGTA | 79658 |
| rs532214665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147755426 | TACTCGGGAGGCTGA[A/G]GCAGGAGAATCGCTT | 79658 |
| rs532215876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147929941 | TATTTGCATTTGTGC[A/G]TACACATGTGTGTAT | 79658 |
| rs532223738 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148020295 | TTTTCTGGTGTTTTT[C/T]TTCCCTTCAGCTTTT | 79658 |
| rs532251026 | in-del | -/AGG | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148007070 | AGTTAGCGCACTTCA[-/AGG]AGGTTAATCATCCTA | 79658 |
| rs532252272 | in-del | -/GT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147899328 | TGTGTGTGTGCATGC[-/GT]GTGTGTGTGTGTGTG | 79658 |
| rs532256254 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148006850 | TGGGAGAGTCAGCTC[C/G]ATGGCTAAGATTTCC | 79658 |
| rs532257573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147859464 | TTTTTAGTAGAGACA[A/G]GGTTTCATGATGTTG | 79658 |
| rs532265544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147851015 | ACATTTGACCAAGTA[A/G]TGAAAATATGGGTTT | 79658 |
| rs532269547 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148033093 | GGATTCTTATTTATT[C/G]TCTTCTTCACTGAAG | 79658 |
| rs532286328 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147880546 | ATAATGATAAATATG[C/T]TATGGAATATAACTG | 79658 |
| rs532295559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148067045 | GAGCTCCTCGTTCTG[C/T]CCCTCCCCTAAGGCT | 79658 |
| rs532313821 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147982900 | TTTTTCCTGAATTTT[C/T]GAGACAGGGTCTTAC | 79658 |
| rs532318949 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147849775 | TTGAAAAGCCCCCAG[C/G]TATTGTCTACTGTTT | 79658 |
| rs532334403 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147797700 | ACAAGCATGAGCCGT[C/T]GCGCCTGGCCAGCCA | 79658 |
| rs532343039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147989810 | TACATCCTTCTCGGC[C/T]GACAGGATTAAGACA | 79658 |
| rs532350736 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148054249 | CAGGCCTGGCCTTGC[A/G]TCCACGTTCTTTTTC | 79658 |
| rs532352796 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148067895 | GCCTGGACTTAAGTT[A/G]TGAGTTCCAGTTCTA | 79658 |
| rs532353328 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148036764 | AGGTTTTCTTTGGCT[C/T]GTTAGGGGTTGATTG | 79658 |
| rs532356726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147888533 | TTTCTTAAAAGTCAT[A/G]CATGCTTATTTTAAG | 79658 |
| rs532370250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147885205 | GTATTAGTTCATTTT[C/T]ATACTGCTATGAAGA | 79658 |
| rs532371982 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147802509 | TAGCATTGGGCAGGG[C/T]CCCCTTTGGACCATG | 79658 |
| rs532372088 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147809863 | ATGCCCCTGCTGATC[G/T]GGGACCCAGGGCTTG | 79658 |
| rs532373805 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147763372 | GCTGGAGTGCAGTGG[C/T]GCAATCTCAGCTCAC | 79658 |
| rs532384595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147804369 | ATTATTCCATGGTGT[A/G]TATGTACCACATTTT | 79658 |
| rs532387597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148019620 | CTGGGCATGGTGGTG[C/T]GTGCCTGTAATCCCA | 79658 |
| rs532393734 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147901310 | ATATGAGCAGTCTTT[A/G]TGAGAGGGTGGGAAC | 79658 |
| rs532393829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147895457 | CAGGAAGATCACTTG[A/G]GCTCAGGGTTAGAGA | 79658 |
| rs532409426 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148021903 | ATCATTTTTTAAAAA[A/T]TTCATTTACACATGA | 79658 |
| rs532411859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148025157 | TCTCTTATGGGAACA[C/T]TCAAGCTAGTGTACA | 79658 |
| rs532432211 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148006235 | GAGAGGCTACAGAGA[C/T]GGGGAGAGATACCCG | 79658 |
| rs532437620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148027612 | TATCTTGATCTAGGT[A/G]AGTCTCTAAAATCAG | 79658 |
| rs532446885 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147891695 | AAAGAAGGGTCTTAA[A/G]TCACTATAAACTATC | 79658 |
| rs532460549 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147942733 | GTTATTCTCCTCGAG[G/T]CCAGGTAAAGGAGCA | 79658 |
| rs532481080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147937744 | CAGCACTTTGGGAGG[C/T]GGAGGCAGGCGGATC | 79658 |
| rs532485197 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147776669 | ACAAGAGAGACTCTC[C/T]TATTCCCTTTGTTTC | 79658 |
| rs532494595 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148040347 | GGTTTTTTTGTTTTT[C/T]GTTTTTTGTTTTGAG | 79658 |
| rs532507951 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148012480 | TATGTGTGACCTCCA[C/T]ATAGACTTAAGTTGA | 79658 |
| rs532512066 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147897947 | CTAGCTCTGCCTCCT[A/G]GGTTCACGCCATTCT | 79658 |
| rs532515946 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148028202 | AGGTAAGGGGAGTAG[C/G/T]GTGACTGAGGCATGG | 79658 |
| rs532518633 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147944804 | TGTGTAGAAAACCAG[G/T]CAAATTGATATTGAT | 79658 |
| rs532525780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148062957 | TGAGTTTGGGGCTGT[A/G]GCTGGTTTCTGGGTT | 79658 |
| rs532528339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147751276 | TATAAGTTTAGCTAT[C/T]GTTAAACATTATCTG | 79658 |
| rs532534882 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147977549 | CTGGGCTCCTTATAT[A/G]ACATTTAATTGGACA | 79658 |
| rs532544839 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147984796 | ATATAGTTGAGTAGA[A/C]ACTTGATCCTTGTTT | 79658 |
| rs532580112 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148013966 | ACTTTTTGATCTTCT[G/T]TGCTGCTAGTGGCAC | 79658 |
| rs532585034 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147810773 | TCCCATCTTTTAGAA[C/T]AGAGCCCACAGGGTT | 79658 |
| rs532585581 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147903607 | AATCTTGTGCTCCAC[C/G]TGTTCATCCCTTTCC | 79658 |
| rs532592662 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147757418 | CCAGGCTGGTCTTGA[A/C]CTCCTGAGCTCAGGC | 79658 |
| rs532594157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147764786 | GTGATCCACGTGCCT[C/T]GGCCTCCCAAAGCGC | 79658 |
| rs532597870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148026822 | TAGGCTGCTAAGTGC[C/T]GAAAAGATTAGAAAT | 79658 |
| rs532636660 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147733959 | GCTTATTTGGTTGAG[A/G]GCTCTCCAGGCCCTT | 79658 |
| rs532640165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148028096 | TGGCAGTAAGTGCCC[A/G]GTGCTAGCTCTGAGG | 79658 |
| rs532654940 | in-del | -/TGT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147759941 | TTTTAGTAGAGACGG[-/TGT]TTCACCATGTTGGCC | 79658 |
| rs532665415 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147811568 | ATTTGAAAAATACTG[A/G]CAAATATGCAATGGC | 79658 |
| rs532672349 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147842453 | GTGTCTATATTATTT[A/C]TAACCTACCTCTACT | 79658 |
| rs532683291 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147912382 | CCATCTCTACTAAAA[A/G]TAGAAAAAATTAGCT | 79658 |
| rs532691634 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147865825 | AAAACTCAACCTCCT[A/C]AAAGCTTTCTTTTTA | 79658 |
| rs532693637 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147949004 | CCCAAAAAACAGAAT[C/T]CATTGTAGTGGTGGT | 79658 |
| rs532696410 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147944255 | GATTTCTTGAATGTA[A/T]CTGTGGCTTGTCTGA | 79658 |
| rs532704226 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148002623 | TCGGGGATTCAGCTT[A/C]TTCCTGGTTTAGTCT | 79658 |
| rs532714650 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147860243 | ATCAGGAGATCCAGA[C/G]CATCCTGGCTAACAC | 79658 |
| rs532715738 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147786737 | TCAACAGTGATTACT[A/G]TCTTGAACCTGTAAG | 79658 |
| rs532727818 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148033908 | TTACGTTGTCCCGGC[A/G]TTTTGGGGATCCCTA | 79658 |
| rs532729602 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147818666 | CTTTGTAACTAACTT[A/T]GTCAGAAACTGCTTG | 79658 |
| rs532735312 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147815169 | TGTCACCCTGCTGCC[A/G]CCCTTGTCCACCTTC | 79658 |
| rs532741487 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148041808 | TGTTTGTTCAGGAAT[A/C]CTAAATATTTGCAAA | 79658 |
| rs532779521 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147886681 | AGAGAAGCAATTTCT[A/G]CTGTATTCATGGGAT | 79658 |
| rs532802142 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARHGAP10 | GRCh38.p7 | 4:147731938 | GGCGTCCAGGGAAGG[G/T]AAGGGAGGAAGAAGG | 79658 |
| rs532808565 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147834782 | CACACCCACCCATCC[A/G]GCTTGCTTTCCTTCC | 79658 |
| rs532817806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148029367 | AGCGGTGCACTCTGT[A/G]ATCTCAGCTCCCAAG | 79658 |
| rs532817848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147765800 | ATGAGACCCTGTCTC[A/G]ATAAAAACAAAAGAA | 79658 |
| rs532840947 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147980850 | AGATGTTCATAGTAG[G/T]CTCTGGAGATCTTTT | 79658 |
| rs532845667 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147868825 | AGAATCTGATGCCAC[C/T]GCGGATCTGACAGAA | 79658 |
| rs532851772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147957952 | GAGAAAATTAAGAGA[A/G]TTAATGTAACTTTCT | 79658 |
| rs532881102 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147883711 | TTTCTTTCTTTTTTT[C/T]TGAGACGAGTCTCAC | 79658 |
| rs532883983 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147780728 | CATCTTGTGGGTGGT[A/G]TAAGCAGGGCAGCAG | 79658 |
| rs532885374 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147808600 | GTAATGTGTTCACAG[A/T]GGAGATAGAGAAGTG | 79658 |
| rs532889213 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147957351 | CACTCATTGCCTCTT[C/T]TAGAGAGTGTGGGAA | 79658 |
| rs532902801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147861702 | AGAGGAGACCTGTAG[C/T]GCATAGCTCCTTTCC | 79658 |
| rs532902832 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147969129 | GACAGGCAAACAGAA[A/G]TGTAGTCCCTTTGGG | 79658 |
| rs532920988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147867648 | AGGCGGGCAGATCGC[A/G]AGGTCAAGAGATTGA | 79658 |
| rs532931172 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147992475 | TGCAATGGCGCTATC[G/T]CCGCTTACTGCAACC | 79658 |
| rs532937188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147826989 | TCTATAGGTTCTTCT[C/T]CCCATCCGCTTTTTT | 79658 |
| rs532937272 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148049979 | TTCAAGTGATTCTGG[C/T]GCCTCAACCTCCCCA | 79658 |
| rs532958060 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147756321 | TGTGGGTGGTGGGGG[C/G]AGTATAAAATATTGG | 79658 |
| rs532967927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147995792 | CGCGATCTCTGCTCA[C/T]TGCGAGCTTCGCCTC | 79658 |
| rs532968190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147992864 | TACTTAAATAATGAA[A/G]GACACCCATCATCTA | 79658 |
| rs532969721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148036382 | ATCTCATCTTGAATT[A/G]TAGTTCCTATAATCC | 79658 |
| rs532973514 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148050442 | GCAGTGGTGCCATCT[C/T]AGCTCACTGCAAGCT | 79658 |
| rs532975280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148042736 | TTAGGGACTGCTTGT[C/T]TGCCTGTATAATTCA | 79658 |
| rs532978518 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147905738 | TTTGGTTCCATATGA[G/T]CTTTAAAGTAGTTTT | 79658 |
| rs532979131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911004 | TTTCTTCCTTCCTCC[C/T]TCCTCCTCTTCCTCC | 79658 |
| rs532986642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147773271 | TTATCATGTCTTCTT[C/T]TAAACACTTTACAGA | 79658 |
| rs532993685 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147942965 | CACAGATTTGGTAGA[A/C]GTTGTTATTGTTTTT | 79658 |
| rs533002976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147833652 | TTATGCACAAGAGGG[A/G]TACATGATGAAAACA | 79658 |
| rs533003756 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911455 | GCAAGCTCCGCCTCC[C/T]GGGTTCACTCCGTTT | 79658 |
| rs533009289 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147833075 | TCTTGGAAGAAAATC[C/T]TGGATACAAGAATGG | 79658 |
| rs533012554 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147916583 | TGCCCAGATTATTCA[C/G]AGGACAAATACTCAG | 79658 |
| rs533012718 | snp | A/G | 0.142947 | 0.22592 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147905076 | CCACTTTTTGATGGG[A/G]TTGTTTGTTTTTTTC | 79658 |
| rs533034833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148014779 | GCATCACTATTTAGC[A/G]TATAGAGTGCTACCG | 79658 |
| rs533047315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147868353 | GTACTCCTCCTGCCT[C/T]AGCCTCCTGAGTAGC | 79658 |
| rs533050046 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147752787 | CCACCTTGGCCTCCC[A/G]AAGTGCCGGGATTAC | 79658 |
| rs533056271 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147799572 | CCTCAAGTTCAGTGA[-/T]TTTTTTTATCCTGTC | 79658 |
| rs533058675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147998488 | AACTGCAAATTCTTT[C/T]TGTGACGTCAGCAGG | 79658 |
| rs533060500 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147744968 | GGGTCAGGGCAAATC[C/T]GGAGGAACTCCATCT | 79658 |
| rs533062482 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147785537 | GCATCCCATGGGTGT[A/G]TGTATATGATATCTA | 79658 |
| rs533063573 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147931448 | AATTTGGATATTTTA[A/C]CTTTAATTTTTCAGT | 79658 |
| rs533071866 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147835652 | GTGCTGGGATTACAG[A/G]CATGAGCCACTGCGC | 79658 |
| rs533094226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147999165 | GGGCTTGCAACTTAG[C/T]TCACACCTGACCAAT | 79658 |
| rs533094245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147874150 | GCTTAGGACCCTTGG[C/T]AGCCCCTTTTATTGT | 79658 |
| rs533112007 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147759997 | TCAGGTGATCCACCC[A/G]CCTCAGCCTCCCAAA | 79658 |
| rs533113964 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147786002 | CTGATTTCGGGAAAA[C/T]TGAGATTTGTGTGTT | 79658 |
| rs533117657 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147837848 | TCAAGTGCTGGGCAG[C/T]CCAAAAGGACTGATG | 79658 |
| rs533120528 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148003561 | TAAGTCTCTTTGTAG[G/T]TCTCTAAGGACTTGC | 79658 |
| rs533124992 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147791687 | CCTCCTGGGTTCCAG[C/T]GATTCTCCAGCCTCA | 79658 |
| rs533133408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147740571 | TCTGGGGCCATTATT[A/G]TAATTTAAACTGATT | 79658 |
| rs533140102 | in-del | -/TAT | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147893442 | ATATTTCAATATATA[-/TAT]TATTATTCTCTCTAT | 79658 |
| rs533145170 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147917099 | CACCATCAAAGATCG[C/T]ATGCACTTGGAACAT | 79658 |
| rs533169013 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147960368 | ATCATTTCTCATTCT[C/T]AAATACTATTATTAG | 79658 |
| rs533184804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147965578 | GAGAAATTAGCCCTT[C/T]CTTTAAGTATAGAGA | 79658 |
| rs533186764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147965381 | TATTATACATTACCC[C/T]ATACACAGATTCTGG | 79658 |
| rs533201726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147745466 | GGAAGATTCAGGGGT[C/T]CATCTCAGAGCACAA | 79658 |
| rs533205148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911606 | TGACTTCGTGATCCG[C/T]CCACCTTGGCCTCCC | 79658 |
| rs533216763 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147971523 | TCTGGAAAGTTTCCC[C/T]AGTAAGTGTTTTGAA | 79658 |
| rs533226334 | snp | C/G | 1.6945e-05 | 0.00291071 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147966664 | AAACAGATTCCTCCC[C/G]CCTTACCAATTTCAG | 79658 |
| rs533229760 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147751843 | GTACTCATCTAGGTA[G/T]CTGAGGCTCCTGCAA | 79658 |
| rs533231453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147792125 | TACACATTGCTTTAC[A/G]CAGTAGTCAGATTAC | 79658 |
| rs533232337 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148051087 | AAACTTACAGCAGCC[A/G]TGGTTCTGACATAGG | 79658 |
| rs533235329 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147746463 | TGGAATGCAGCGGCG[C/T]GATCTTGGCTCACTG | 79658 |
| rs533240823 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148069096 | ACTGCTTGGGGGAGG[A/T]GTGGTGTGATAAACT | 79658 |
| rs533249627 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147977011 | AGAACATGTTCATGT[A/T]AGGGATGGGATTGAG | 79658 |
| rs533286326 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148004609 | ACGTGGCAGGAAACC[A/G]CAGGCATCCTCTAGG | 79658 |
| rs533287373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148011547 | AAACAAGCTAGAGAC[C/T]GTAGGGCCTTTCATG | 79658 |
| rs533289524 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147755058 | TTGCACTACAGTCTG[C/G]GCGACAAGAGTGAAA | 79658 |
| rs533293383 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147878526 | TATGATTCTATAATT[A/C]TATCATTTTGAGAGG | 79658 |
| rs533297076 | in-del | -/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147796860 | CTAGTACTGGCCATA[-/G]TTATAACATTCTATG | 79658 |
| rs533304581 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147885749 | TCTCCAGTTCAGCTG[C/T]TGCTCCTTTAAATGT | 79658 |
| rs533309764 | in-del | -/AAAACAAAAC | 0.0228947 | 0.104514 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147860436 | GACAGCTCCGTCTCA[-/AAAACAAAAC]AAAACAAAACAAAAC | 79658 |
| rs533313268 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148046025 | TGCCTGGAGCAGTTA[A/C]AATTTAATGGGGACT | 79658 |
| rs533317520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148005156 | ACATTTATGCCTCAG[A/G]GTCTTTGCACTTATT | 79658 |
| rs533318663 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147859771 | GTGGAGATGCTTGTA[C/G]AGTGAGCTGGGGCTC | 79658 |
| rs533329235 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147753372 | TTTTTTTTTTTGAGA[C/G]ACAGTCTGTTGTCCA | 79658 |
| rs533345860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147829348 | GTGAGCCACCGCGCC[C/T]AGCCAATTTGTTGTA | 79658 |
| rs533345916 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147820916 | TTTAACACAACCAAA[A/T]TTTATTAATTTTTCT | 79658 |
| rs533360522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148051883 | AACCATTTTTATTCT[C/T]GTCAATGCAATCACT | 79658 |
| rs533375834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147848841 | TAACATTTGTTCAGA[A/G]TATATCCTGCAAAGC | 79658 |
| rs533386163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148058763 | TAAAGTAACCACATA[C/T]ACAGCACTGTCATAA | 79658 |
| rs533388649 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147841438 | CTTCATCCATCTCCT[C/T]GACATTGGGAAACTG | 79658 |
| rs533394922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147961262 | GTGAGTATTACTCTT[C/T]CATTGTGTTGTTAAC | 79658 |
| rs533400349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147760061 | GGCCTTTTACTGTGT[A/G]TTTTATACATATAGT | 79658 |
| rs533400795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148045129 | TTTCAGTGGTACAGT[C/T]GGTTAGTGTGCAGCA | 79658 |
| rs533400871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147918626 | CTGGTCTGGACTTAG[A/G]GGCCCTTCATCTCCC | 79658 |
| rs533416883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147835263 | TTTTTTACTGTTGAC[C/T]GCCACTTTTTTCTCT | 79658 |
| rs533427281 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148059126 | TTGAGAAAGAAGGAC[A/G]GTGATGTTGGCCTTC | 79658 |
| rs533434682 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147848298 | AGTTTTTAATGAAGG[G/T]CTACGAATTGAGGCT | 79658 |
| rs533434884 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147765784 | CAGCCTGGGCGACAC[A/G]ATGAGACCCTGTCTC | 79658 |
| rs533435053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147855462 | AAATTAAAAAAACCT[A/G]GAGCGTAAAGAAAAA | 79658 |
| rs533444158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148016770 | GCTGGTCGCAGGTCC[A/G]GGCCTCCAGAAATTC | 79658 |
| rs533447151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147854941 | ACTTTACCCACATGT[C/T]GATTTTCATAGCCTT | 79658 |
| rs533471591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148070614 | AATCTATGGGGAAAA[A/G]AAGAGTAGAATACAG | 79658 |
| rs533476763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147925608 | TTTCTTACAGGGAAG[A/G]TATTAGAGGAAAAAA | 79658 |
| rs533482534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148009932 | ACCTCAGTTTCTGGT[A/G]TCTGAATAAGGAACA | 79658 |
| rs533492753 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147816630 | GCCTAACCTAGCCCT[A/G]TGATGCATTCTGGGC | 79658 |
| rs533499160 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147891920 | ACATGCTGTTAGCTT[C/T]GCTGGCATGCTTGCC | 79658 |
| rs533515244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147788289 | GTCTCTATTAAAAAT[A/G]AAAAAAAATTAGCCA | 79658 |
| rs533526500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147800145 | TGTGGAGGCAGAAGG[A/G]ATTTCCCTAGGCTGG | 79658 |
| rs533553059 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147979728 | GCAGTGTTTTGTAGT[G/T]CTTCTCACGGACATC | 79658 |
| rs533565561 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147794495 | AGTCACATTCACCAG[C/T]GTAAGTAGCATCCAG | 79658 |
| rs533575626 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148053139 | AAAAGATTGGAAGGC[A/G]CAAAGGACATAGGAA | 79658 |
| rs533578446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147892821 | CTGGAGACACTGATA[C/T]AATGTATTTTAACTG | 79658 |
| rs533579183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147806500 | CTGTTTTTGGGGGGG[C/T]GGGGGATGGAGTTGC | 79658 |
| rs533579723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147836101 | GAATAAAATTTCTGC[C/T]ATCTTTTTTCAGTTA | 79658 |
| rs533583137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147876452 | CAAAAAATCAGCAGG[A/G]CGTAGTGGCGGGCAC | 79658 |
| rs533588454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147829216 | CCACTATGTCCGGCT[A/G]ATTTTTTTTGTATTT | 79658 |
| rs533590382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147918997 | CTCATTTTTCCTCTT[C/T]TACTAAATTCTCTTC | 79658 |
| rs533610590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148017121 | ATCATCAAGCAGAAA[C/T]ATAATTGTACAAAAA | 79658 |
| rs533631902 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147759225 | GTTTTATCTGAGAAC[G/T]CCGTATGTTGTCTCA | 79658 |
| rs533633064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148009686 | TACATTTCCAGATGG[C/T]CACCGTTTTTTAAGT | 79658 |
| rs533633648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148022910 | TCCATAAAATTTAAT[A/G]GAATACTTGTTTTTA | 79658 |
| rs533643517 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148029964 | CCCCTGCGTTGGTGT[A/C]TCCCCAGAAACCTCC | 79658 |
| rs533684620 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147928529 | GCGAACATGCCAGTG[-/A]AAGCAAGACTTATAT | 79658 |
| rs533695384 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147805991 | CCATGTTTGTACTTA[C/T]ACAATATTTTCCACC | 79658 |
| rs533712038 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147899646 | AGAAACTTTTTTTTT[A/T]GGTGAACAGAAGAAA | 79658 |
| rs533729417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147986738 | CTCATATTCTGTAAA[A/G]TACATCATGATTCAG | 79658 |
| rs533732451 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147875909 | GTCAACTGTACAACC[C/T]AATTGCTAGTTAGCA | 79658 |
| rs533733556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147800616 | TGACCACTTTGCATA[A/G]GGGGATGCAAGATAC | 79658 |
| rs533736550 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147852279 | CTGGAGCCACCACTG[A/G]GGAACCGAGGTGGCA | 79658 |
| rs533738121 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147780162 | AAAATTAAAAATCTG[G/T]GAGCTACCCATAAAT | 79658 |
| rs533738686 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147865168 | GCACTGATAATACAC[A/G]TAATATTCCCATTGC | 79658 |
| rs533745749 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147799911 | TGCCTATCTTTTTTT[G/T]GGGGGGGTGCGGGCA | 79658 |
| rs533756740 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148058984 | CACAGGAAATGCCTC[C/T]GTGGCGTCAGGAACA | 79658 |
| rs533760665 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147980891 | GGTATCGGTTGTTAT[G/T]TCACCTTTGTTATTT | 79658 |
| rs533766778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148052185 | AGGGTGGGAGTCACT[A/G]GCAAACCCTGTCTTC | 79658 |
| rs533776222 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147875273 | CTTTCTCTCCCTGCT[C/G]CTATCACCTAATGGG | 79658 |
| rs533778887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147760379 | TAACCAGCTTGTCCA[A/G]ATTTATCAGGTTTCT | 79658 |
| rs533789664 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147892536 | GAAGCAAGTAACAGT[G/T]CAGAGGTCTAAGGTG | 79658 |
| rs533795398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147872195 | GGGACCTCATGGAGG[C/T]GTCTGCGGCAGGGAT | 79658 |
| rs533802532 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147787868 | AGTTAATGTGAGGCA[A/C]CCGACCTGTGAGGGT | 79658 |
| rs533805001 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147961469 | TATGTATTTCAGATA[G/T]TTAGTACTTTGTACT | 79658 |
| rs533828020 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148005370 | AGGAGGGCCACTTGA[G/T]CCCAGGAGTTTGAGA | 79658 |
| rs533840667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147986437 | GCATTTAATATTAAA[C/T]GACTGCAATTACTTG | 79658 |
| rs533845166 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147835630 | CTGCCCGCCTTGGCC[G/T]CCCAAAGTGCTGGGA | 79658 |
| rs533866500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147746692 | ACCGTGCCTGGCAGC[A/G]TGCTTCTTAATATAG | 79658 |
| rs533871383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147939710 | TCAAAGGTTATTTTT[A/G]TAGTTAACAGGAATG | 79658 |
| rs533872938 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147891748 | TCAGAGACCATGGGC[C/T]ATGAAATGATTAGGT | 79658 |
| rs533881797 | in-del | -/A | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147822499 | GGGGAGGGAATAAAC[-/A]TTTTTTCAGCATCTG | 79658 |
| rs533904248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147974808 | CAGGGCTGGGGAGGC[C/T]TCACAATCATGGCGG | 79658 |
| rs533914770 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147982959 | AATCACAGCTCATTG[A/C]AGCCTCGACTTTCTG | 79658 |
| rs533916746 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147888672 | CCCCGCCCTTTAATG[C/G]TTTATTTCCTCATTT | 79658 |
| rs533919738 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147973607 | TTCAGTCATCCTGTT[G/T]TGCTATCAAATACTG | 79658 |
| rs533922601 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147967078 | GAAGAAGCATTTAAT[A/C]CAGATGTAAGTGAAT | 79658 |
| rs533925584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147881408 | TTTGGGAGGCTGAGG[C/T]GGGTGGATCATCTGA | 79658 |
| rs533928748 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148071391 | GGGGCCAAGGCGAGT[A/G]GATCACCTGAGGTCA | 79658 |
| rs533949765 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148061104 | AGGTTTCCTTTTTTT[G/T]TTTTAAAGAAAGATG | 79658 |
| rs533965552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147843814 | CCACTGCACCCGGCC[C/T]GAACCCCTTTCTTCT | 79658 |
| rs533965851 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147887003 | CTCAAGAGATCCACC[C/T]GCCTCGGCCTCCCAA | 79658 |
| rs533972301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147754831 | GGGCGTGGTAGCTCA[C/T]GTCTGTAATCCCAGC | 79658 |
| rs533973768 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147768724 | AAGTGCTTAAAAATG[C/G]GGGCAAATTTTCTTG | 79658 |
| rs533988908 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147973089 | GAGAGCCAGAGTGTG[G/T]ATCAACTTGTAAGAT | 79658 |
| rs533992826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148065029 | CTTTGCATATTGAAA[C/T]AAGGGTGTAGCTTTT | 79658 |
| rs534007697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148032661 | GGAGTATTGACTCAC[A/G]TGATCACAAGGTGAA | 79658 |
| rs534008004 | snp | A/C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147952356 | TCCCAAGTTGATGTA[A/C/T]TTCTTTACATCCTCA | 79658 |
| rs534009414 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147752876 | TAAATTTGCTGCTTA[G/T]CTCATGCCTGTGTTG | 79658 |
| rs534014477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147849318 | ATAGCCTATCCAACT[A/G]ATAATTCTAGAAGAA | 79658 |
| rs534030426 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147762317 | CCTGCCCAGAAATTC[A/G]TTCCTTTTGAAATCT | 79658 |
| rs534037347 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147792700 | AAGTTGTTGTGTTGG[C/T]TTTGGTCTCATTCCT | 79658 |
| rs534042665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148025290 | TATGTTCATTATTTG[C/T]ATGATGTTTTGTTCT | 79658 |
| rs534047894 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147934791 | GAGAGCTGTTATCAC[A/G]CCACTGCATTCCACC | 79658 |
| rs534058699 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147942163 | TAGTGTTTATTATTA[C/T]TCCTGCAGGTAATAG | 79658 |
| rs534059175 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148070245 | CTGGTCTGGAGCCAG[G/T]AGAGGAGTCCTGGAA | 79658 |
| rs534060819 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147806188 | ATCTTACCACCTCAG[C/T]GTCCAGAGTCCAGGC | 79658 |
| rs534065914 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147758082 | AGCCTGGCCAACATG[C/G]AGAAACCCCGTCCAT | 79658 |
| rs534068791 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148066312 | GCAGAACTGAGTCAC[A/C]TGCTTACCCTACATC | 79658 |
| rs534073687 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147836639 | GTTAGAGCTTTGTGC[A/G]TGGGTTCCTTAAATC | 79658 |
| rs534075746 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147932421 | CCCATCAATGATAGA[A/C]TGGATAAAGAAAATG | 79658 |
| rs534079749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147856162 | TTGGCTGACAGCTTT[A/G]GGGGAGACACCCATC | 79658 |
| rs534079786 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147848623 | ATTGGCAGGTATTCC[A/G]TGTAAACAACATCCA | 79658 |
| rs534082479 | in-del | -/G | 0.00636936 | 0.0560724 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147756315 | GAAGGTGTGGGTGGT[-/G]GGGGGGAGTATAAAA | 79658 |
| rs534085559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147940380 | CCTCCAGAACCATGC[A/G]TGCTCCATCTGTGCT | 79658 |
| rs534086328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147863790 | TTAGCTTAGTAACAC[A/G]TTATGTTTCAATATT | 79658 |
| rs534087595 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147759804 | CCCAGGCTGGAATGC[A/G]GTGGTGGGATCTCAG | 79658 |
| rs534091889 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147855244 | ACAGAGTAATGAGTG[G/T]CTAGGACTGCAGCTT | 79658 |
| rs534110089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147815813 | CAAGGCTGCAGGGAG[C/T]TATGATAGTGCCACT | 79658 |
| rs534112027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147947133 | TGAAAAAGAAGTTTA[C/T]TTGGTGAGGTTTTAA | 79658 |
| rs534124003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148070866 | TGAGCTGGGGCCTGC[C/T]CACAGCTGGGGGTTA | 79658 |
| rs534125176 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148038471 | CAGAGCTGTTAGTCT[C/G]CCACTGTGACTTTTA | 79658 |
| rs534126616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147987031 | ATAACGGGATTATTG[C/T]GGATTGAACTGAATC | 79658 |
| rs534134774 | snp | G/T | 1.65482e-05 | 0.00287643 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147955421 | TTTTGTAGTTGGTAG[G/T]GAGCATAAACGAAAA | 79658 |
| rs534135229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147959387 | TTTTTTAAAATTATA[C/T]TCTAAGTTCTAGAGT | 79658 |
| rs534147942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147927872 | ATTAGATACTGGGAT[C/T]GGGAGACCTCTGGGA | 79658 |
| rs534164190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147907737 | AAAAATTGATGCTAT[A/G]TTGGGGAATGTATCA | 79658 |
| rs534165110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147822625 | TCTCATAGATTGAGC[A/G]GAGGAGAGCTCTACA | 79658 |
| rs534175186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147882756 | AATCTTTGCCAGAGA[A/G]GAAGAAGTAGAAGAG | 79658 |
| rs534180237 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147795216 | GCCTCCTGCAGCGCT[G/T]GGATTACAGGTGTGA | 79658 |
| rs534184931 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148037852 | AAAAAAAAAAAAGAA[A/G]AGAATGGATGTCAGC | 79658 |
| rs534185403 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147962037 | GGTCACACCTCCTGG[A/T]GAACATTTCTAGCCT | 79658 |
| rs534190416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147802045 | GCCCTGTTTAATGTC[A/G]CTTGAGTAATGATGC | 79658 |
| rs534201787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147913422 | CCACAGATTGGGTGG[C/T]TTAAAGAATAGAAAT | 79658 |
| rs534209389 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147968087 | GGCCCATGGCAGTTT[G/T]TGTTTGAATTGAGAA | 79658 |
| rs534209994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147734074 | GGGGGTGCAGAGTGA[A/G]CACGAGAGAATGAGG | 79658 |
| rs534213316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147888205 | CGCTCTTCACTCACA[C/T]TTTTTTATGACCTTG | 79658 |
| rs534228704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148019014 | TGTATTCAATGAATT[A/G]GGAAGTAATTTATAT | 79658 |
| rs534244313 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147815466 | CCTGAGATTATTGGC[C/T]GGAGGCGGGGGGCGG | 79658 |
| rs534260720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148066856 | GGTTTCTGAGTTGCT[A/G]TAGACGTATGGGGGA | 79658 |
| rs534267484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148024647 | TAATTTCCAGAGGAA[A/G]GGCATGAATCATTAC | 79658 |
| rs534273324 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147780848 | CCTCTGAGAGCAAGT[A/C]CACCTAGGGTGGACT | 79658 |
| rs534276536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147859886 | CATACACTTTTTAAT[C/T]TTGCTCTGTTTGCTT | 79658 |
| rs534277984 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147996702 | GACCCCTCCCAAAAT[G/T]CATATGTTGAAGCCC | 79658 |
| rs534278693 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147890037 | AGCACTGTTCCATTT[A/T]TCACATAGCACTGTC | 79658 |
| rs534281094 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148072368 | TCCAGCATATAGAAT[A/G]AGAGGGAGGGCAGCC | 79658 |
| rs534286140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147990132 | ATGAAGAAGGCACCC[C/T]GTCCTTCAGGTCAGG | 79658 |
| rs534294405 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147770209 | TAGACTTGCTGATAC[A/G]GTAGTATTTGTCTAT | 79658 |
| rs534296129 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148018228 | GCTTAAGATGAGTTC[A/G]TCTCTCTTAGAACAA | 79658 |
| rs534308286 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147761487 | GCATTTGATTTCAAC[C/G]TTGTGGGTCTGAAGC | 79658 |
| rs534317685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147896718 | AAGCACAGATCATTA[A/G]TTTTACACCTTGTTT | 79658 |
| rs534357388 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147903129 | CATGGCCAGGGAGGC[C/G]CTGTGTGGCTGGACC | 79658 |
| rs534357652 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147900114 | GTAAAGCCTGTCTTC[C/T]ACATGGTTTGATAGA | 79658 |
| rs534360262 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147775555 | GGCCTGGTAGGAGAA[A/G]GGTGATTATTGTCAG | 79658 |
| rs534380450 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147901732 | ACTTCTAGTCATAAC[A/T]CTTTAAGCCCTTCAT | 79658 |
| rs534383355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147909244 | AAAGTCTGAAGTGAG[A/G]TTGAGGTGGGTGCAC | 79658 |
| rs534399761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147769538 | CTGACATTGTTTCCC[A/G]GGGATTTCCGTATGT | 79658 |
| rs534441010 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147996217 | ATAGCTAGGATATGG[C/G]CTATGGAAACCTCTA | 79658 |
| rs534441283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147871955 | AAAATAGAGAAAAAT[C/T]AGCTGGAGGTGGTGG | 79658 |
| rs534477200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147774965 | GGTTGGAGTGCAGTG[A/G]CATGATCTGGGCTCA | 79658 |
| rs534478507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147871535 | TTGGAAATGTTTAAT[C/T]ACTAAAGGATGTAAA | 79658 |
| rs534481078 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147907148 | GTAACAATTTAAAGT[C/T]TCATCTAGTAGTTTA | 79658 |
| rs534483682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147736071 | CTTACAGTTATTAAG[C/T]ACTAATACAGTGATA | 79658 |
| rs534484469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147870889 | GCAAAATATTTTTGT[C/T]GCAATGTTCTAAGGA | 79658 |
| rs534494450 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147969975 | AGGGTTGGAAGCAGG[G/T]TTGTGTGGCAGGGTT | 79658 |
| rs534499230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147873939 | AGAGGGAACCTAGCC[A/G]TCAACAACTGAGTTC | 79658 |
| rs534518929 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147912682 | TTTTGGGGAGACAGG[G/T]TATTGCTCTGTCACC | 79658 |
| rs534551213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147954917 | CTATGTATTTTGTGT[A/G]GAATCTTCAGCTAAT | 79658 |
| rs534573950 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147837624 | AGTTGCTGCCACCTC[A/G]CTAGAATCTCTGGTC | 79658 |
| rs534578393 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147950982 | AACAGATCCCAACGA[A/G]TGGCAAAGAGAGGTG | 79658 |
| rs534591608 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147976611 | AAAAGAGACTTTAAA[A/G]GCACAGGAAACTTTC | 79658 |
| rs534595212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148033513 | CAATGGTTATCCTTA[A/G]GTGGTTAGAGTTGGT | 79658 |
| rs534597298 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147749158 | CCATAATAGAGGAGG[C/T]GAGAGAGATGAAATT | 79658 |
| rs534598956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147903743 | TTCTTTCACTGAGTA[A/G]CATACATTTAAGCTC | 79658 |
| rs534613131 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147846717 | AGACTGGTTGTATTT[A/G]AACAAGTAGCTACAG | 79658 |
| rs534614354 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147983746 | TCAATTTTCTCTTTG[A/T]TCTTGTTGCATTTCT | 79658 |
| rs534616866 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147984980 | TTGAGGGGTGGTCCA[A/G]TGGGTGGCTACTAGG | 79658 |
| rs534627270 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147844390 | TTAAATTATTTTGAG[G/T]ATGGTCACTCTGTTG | 79658 |
| rs534631930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147748500 | AATTTTCCTAAGAGG[A/G]TAGATCTTATATTAA | 79658 |
| rs534641900 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148033964 | GAGTTTTATTGAATG[A/G]TTGACTTGCTTGTAA | 79658 |
| rs534647059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147969440 | CCAGACAGCTCATGG[A/G]AAGATGGCTACTGTT | 79658 |
| rs534651376 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148026372 | CGGAGGGGAGATCCT[C/T]TGCTGGGAGACATGT | 79658 |
| rs534657797 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148001091 | TGAATTAATTTTTGT[A/G]TAAGGTGTAAGGAAG | 79658 |
| rs534664135 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147803054 | TGCTCTGTTGCCCAG[G/T]CTGGAGGGCAGTGGT | 79658 |
| rs534715704 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147791744 | CACCCGCCACCATGT[C/G]CAGCTAGTTTTTGTA | 79658 |
| rs534717713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148042303 | AGCTGTTCTCCAGAT[C/T]GTATCACTTCCCTGC | 79658 |
| rs534724817 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148052992 | TTAGATACCCTCTTG[A/G]CACTTCCAGGCTGAG | 79658 |
| rs534728484 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147785217 | TCACTAAATCTAAAA[A/G]TAAAATCACAAGGCT | 79658 |
| rs534743712 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147864545 | CTTCAGTTCTTGGGG[G/T]TCAACTTCAACAAAC | 79658 |
| rs534770219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147832515 | AGCCAGTCGTGGTGG[C/T]GGGCACCTGTAATCC | 79658 |
| rs534771295 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147915675 | TCTCATTTAAAAATA[A/G]GAGACAAAAAGCATA | 79658 |
| rs534778681 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148014329 | CTTCTGACTTCAGAA[A/C]TCGTATGCTGTGTTT | 79658 |
| rs534793289 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147823996 | GTGACACACCATCTA[G/T]TCTCACCATTTATTT | 79658 |
| rs534798116 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147860070 | ATGCTCAAGAGATTC[A/G]TAAGAGTTGCAGAGA | 79658 |
| rs534800904 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147831398 | AGTTCTTATAGGATA[A/G]GTACCTAAGGCATTA | 79658 |
| rs534832246 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147839110 | TCTATCTATCTATCT[A/G]TCTATCTATCTATCT | 79658 |
| rs534834320 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148021631 | CTCCTTCACTGTTAT[C/T]GGACTTCTCAATTTA | 79658 |
| rs534850944 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148056474 | AATTTTTATTTTGGA[A/T]TAGTTTAAGGTATGC | 79658 |
| rs534851934 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147914344 | TTCCTGTATTTGCTG[C/T]GTTGCATTTTTATTT | 79658 |
| rs534853917 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147921699 | ATGTGTTTTAGGTGA[A/T]TCCCAGACAGACTCA | 79658 |
| rs534856808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147930210 | TTCTGTAGAATCATA[C/T]GGCTGCAAAATCCTT | 79658 |
| rs534893634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147921052 | TAATATTGGTAGTCA[C/T]GCATGGGATGCCCCA | 79658 |
| rs534902025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147890031 | GCATATAGCACTGTT[C/T]CATTTATCACATAGC | 79658 |
| rs534903745 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148002612 | TATTGGTCTATTCGG[A/G]GATTCAGCTTCTTCC | 79658 |
| rs534906072 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147796772 | CCTTGTGATCCACCC[C/G]CCTTGGCCTCTTAAA | 79658 |
| rs534908228 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147958014 | AAGGAACCCAGTAGA[C/T]GATCCATCTTGGGGG | 79658 |
| rs534911969 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147993883 | GCTCAGTGAGGAGCT[A/G]GTGTTTCAGACATGG | 79658 |
| rs534918128 | in-del | -/T | 0.470327 | 0.118136 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147983187 | TGCCTGGCTGCTTTG[-/T]TTTTTTTTTTTTTTT | 79658 |
| rs534933409 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148013611 | GAGAATGGCGTGAAC[C/T]CGGGAGACGGAGCTT | 79658 |
| rs534936037 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148012660 | GTTTAGTCTTAATAG[A/T]TATATTAAGTTGGTG | 79658 |
| rs534936773 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147755448 | GAATCGCTTGAACTC[A/G]GGAGGCGGAGGTTGC | 79658 |
| rs534937798 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147897575 | GTATAACATGCATTT[A/T]AAAATAATCATAATA | 79658 |
| rs534947380 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889564 | CTCTGCCTCCCAAAG[G/T]GCTGGGATTACAGGC | 79658 |
| rs534949901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147789124 | AGTGAGCACTGGGGA[A/G]GGAGGCTATTTTTGT | 79658 |
| rs534950419 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147795870 | CAGCTAATTTTTGTA[G/T]TTTTAGTAAAGATGG | 79658 |
| rs534958444 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911553 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCGTGTT | 79658 |
| rs534966727 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148033625 | ACACATACCGCATAC[A/G]TTTATATGTGTTTAG | 79658 |
| rs534976620 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147785584 | TAGTTTATGCTTTCA[A/T]ACAGAAGTCATCCAG | 79658 |
| rs534981672 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147862142 | CCTGTGCTTGTTGGC[A/C]TCCAAAGTCCAGAGG | 79658 |
| rs534981869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147873311 | CTCAAATCTAGGGCA[A/G]TTTGAGCATGAACAT | 79658 |
| rs534982948 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147738552 | AGTGAGACTCTGTCT[C/G]CCCCCCCCAAAAAAA | 79658 |
| rs534992703 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147820164 | GCCTCAGGGAATAGC[A/G]AGTAAAGGGTTTTCA | 79658 |
| rs534999664 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147826606 | CAAACATGTACCAAA[C/G]TCGAGAGAAATATAC | 79658 |
| rs535004058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147964631 | CTGTAACATGCAATA[A/G]CCTATTTGCTGATAT | 79658 |
| rs535010221 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147780885 | AGGGAAGATGCCTCA[C/T]TAGGCTGGTATCATC | 79658 |
| rs535015252 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148020762 | GCAAACATACTCGTG[C/T]GTGTATCTTTATAAC | 79658 |
| rs535021029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147745098 | GAGTGTTCAGAGAGC[A/G]GGAGGGAGTAGACAA | 79658 |
| rs535021120 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147872644 | GCTGATTACCACACA[C/T]TTTGTGTGTTCTATG | 79658 |
| rs535038816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147803446 | AAACATTTATCATGT[A/G]CTTTGGGAACATTTC | 79658 |
| rs535047108 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147860371 | GGCGTGAACCCAGGA[A/G]GTGGAGCTTGCAGTG | 79658 |
| rs535062813 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147924318 | GGACTGTTACTACTT[C/T]CCTGTTGTCCAGTGA | 79658 |
| rs535082504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147839657 | TTATGACATCAGAAC[C/T]TAGACTTTGATTTCC | 79658 |
| rs535091814 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147798188 | AGCTTTATTTAAATG[A/T]AGTGTGTGGACCGTT | 79658 |
| rs535093926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147923312 | AAGTACAAATGAGCC[A/G]CCCCCCATGAGCAGT | 79658 |
| rs535113824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147848428 | TTTGCAGCAGGAGAT[C/T]GGAGGTCAGCTTTCA | 79658 |
| rs535172739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147970953 | CAAGAATTAGCCAGG[C/T]GTGGTGGCGGGCACC | 79658 |
| rs535183107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148062549 | CTTAGAGGCCATTCC[A/G]GGTGTCTGTTCACTG | 79658 |
| rs535188820 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147931922 | AAATTTTTGCAATCT[A/G]TCCATCTGACAAAGG | 79658 |
| rs535199681 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147938911 | TTCAAGCATAAAAAA[C/G]TAGAGAGATTGGTAT | 79658 |
| rs535205443 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147809443 | TTTGTCATCCAGACA[A/G]GATAACTTAGTAATA | 79658 |
| rs535212096 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147964093 | CCCCTCCCAGGGCTG[C/G]CCCATTCCTGGAGAT | 79658 |
| rs535217989 | in-del | -/T | 0.00478085 | 0.0486577 | intron-variant, downstream-variant-500B | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147783001 | ATTATATATATTATA[-/T]TAAATTATATACTAT | 79658 |
| rs535222549 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147998284 | TACAGAAATAATAGA[C/T]ATACAGTGCATATAA | 79658 |
| rs535227070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148055847 | TGGGTATGTGTGGGT[C/T]AGCCCCAGGCACGAA | 79658 |
| rs535227221 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147753856 | GTTTAATAATTCCAC[A/G]TGTATGAGAGTCCTT | 79658 |
| rs535242863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147970522 | ACAGGCGAAAAATGG[C/T]GAGAAGGAAGTCATT | 79658 |
| rs535264372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147812617 | CTTTCTTCTCTTCTA[A/G]TATTTCAACATAGTC | 79658 |
| rs535265451 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148021358 | CAGTCAGTATGATCC[G/T]GTAAGAGGGTCTGTT | 79658 |
| rs535266181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148035508 | CCAAGTGAATTATTA[C/T]CTAGCAACTGACTGT | 79658 |
| rs535266961 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147750311 | CTAGAATGAAGGGAG[A/G]TGTTTAATTTCTTTC | 79658 |
| rs535269146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147845705 | GGTTTATTTGGGATC[A/G]CTAGTTGGGTAGATC | 79658 |
| rs535271648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147945310 | TTTTTTCCTGGTGCC[A/G]TATACCTTTTCTTTA | 79658 |
| rs535277159 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147819608 | GCTGGAGTTCAGTGG[C/T]GCTGTCTCAGCTCAC | 79658 |
| rs535287004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147804971 | GTGCAGAGGCTCTTT[C/T]GTTTAATTAGGTCCC | 79658 |
| rs535300024 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147812073 | CGACTGTTCTCTCGA[G/T]GCAACCTCCTGATGG | 79658 |
| rs535307886 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147936924 | TATGGCCTCAGCTCC[A/G]CCTCCTGTCAGATCA | 79658 |
| rs535322534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148042937 | ATTTGTAGAGGCAGT[A/G]GCTCTCCATGCTGAT | 79658 |
| rs535322853 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147764498 | GGTAAAAAAAAAAAA[A/C]CTCCAAATCTGGAAT | 79658 |
| rs535325870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147898349 | TGTCTTCAGGCTTCC[A/G]TTTATTTTCTGATGA | 79658 |
| rs535334644 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147818990 | TTATATTTTAAAATG[A/G]AGAAATGATATAACT | 79658 |
| rs535340272 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148053822 | ATTTTTGGTATCTGC[A/G]TTGTGTACTTGGCAC | 79658 |
| rs535347896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147852305 | TGGCACTTTGCCAGC[A/G]TTGGTGCTGCTGCAG | 79658 |
| rs535349846 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147844492 | CCCCTACTATACTTC[A/C]CAGCTTCTGGTAACA | 79658 |
| rs535359966 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147904633 | ATCCAGTCTATCGTT[G/T]TTGGACATTTGGGTT | 79658 |
| rs535378264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147861049 | AGTTTTGCTCTGGCC[C/T]GCTGGGCTTGTTCTG | 79658 |
| rs535379324 | in-del | -/ATA | 0.00119737 | 0.0244387 | upstream-variant-2KB | ARHGAP10 | GRCh38.p7 | 4:147730811 | GTGGGTGCCCGGCAC[-/ATA]ATAATTGCTTAATAA | 79658 |
| rs535427377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147886517 | CTGTTGTTCGTCGTG[C/T]ACTCACTTTCTTCCT | 79658 |
| rs535436425 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147748390 | AGAAACTAGTAAAAA[A/T]AAGCTGATGTCTTGT | 79658 |
| rs535445251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147947889 | CTATTATCCTGCTTC[C/T]TGAGTTATCAACATT | 79658 |
| rs535461518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147987575 | CTTGGTGCCTGTCTT[C/T]TCTGGGTCTGCTGCT | 79658 |
| rs535479451 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147901075 | AAAAACTACAGAATT[C/T]TTATATTTTGGTTTA | 79658 |
| rs535481484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147980285 | GCTTTTTCTGTGTCT[A/G]TTGAGATGATCATAT | 79658 |
| rs535491261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148015659 | CTCTGTACTGTTCAC[A/G]TGGTAGCTACTCTGA | 79658 |
| rs535499706 | in-del | -/T/TT | 0.480607 | 0.149361 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147857535 | CTGTTTAATCATAGT[-/T/TT]TTTTTTTTTATTTGT | 79658 |
| rs535509431 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148029557 | AGCTATAGATGTTTC[C/G]TTGTAAACATGTGAT | 79658 |
| rs535547253 | in-del | -/GCCAGGATG | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147983393 | GGTTTCACCGTGTTA[-/GCCAGGATG]GTCTCCATCTCCTGA | 79658 |
| rs535549244 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148022999 | CTAAAGATAGTTTTA[C/T]TTGTTTAGTTTTGGA | 79658 |
| rs535553937 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148015236 | AATCTCCCCAGAAGA[C/G]GAAGTACATGCATGA | 79658 |
| rs535556210 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147765946 | ATTAGTTCCAGGAAC[C/T]CCTTGAATACCCAAA | 79658 |
| rs535558418 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147733166 | ATTCCACCCCGGTTA[C/G]GCTTGGTGCCTTCCT | 79658 |
| rs535560694 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148015703 | GTCGAAGTTCAGGTT[G/T]CCTGGGAGTGAACCT | 79658 |
| rs535566652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147904354 | GTCATTTAGCATTAG[A/G]TATATCTCCTAATGC | 79658 |
| rs535569687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147805501 | AGTTTTTCTAATTCT[A/G]TGAAGAATGTCAATG | 79658 |
| rs535581138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147906116 | AAGGTGCATCTTTTC[C/T]TAACGCTCCTCTGCC | 79658 |
| rs535583566 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147993355 | TTCGGCTAGGTGATG[A/T]TGTATGTAGGAGTTC | 79658 |
| rs535584806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147986125 | TTGGGAAAAAAGGTC[A/G]TGTGACTTTTGAGGG | 79658 |
| rs535590487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147861435 | CTCTTCTCTCCTTCT[C/T]GTCGCCCACAATGTA | 79658 |
| rs535597763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147766659 | ACCCACCCACACACA[C/T]CCACACACACTGCAC | 79658 |
| rs535608395 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147891990 | TGATAAATAATTACC[C/T]GTTCTGTGAAAGTTC | 79658 |
| rs535610829 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147992052 | ACGGGTTAAGGAAAT[G/T]ACAAGCCATGCAGTC | 79658 |
| rs535613763 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147927054 | GTATACTACAACTTG[C/T]TTCCAAGACTGTGTT | 79658 |
| rs535616886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147765376 | TATTTCAATGTGCCA[C/T]GCCCATTTTCATTCC | 79658 |
| rs535617786 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147855222 | TTTGTGACCTTGCTA[C/T]AGAGTCACAGAGTAA | 79658 |
| rs535639099 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147899034 | TCTCTGAGTAGGACA[C/G]AGAGTAGGTGGATTA | 79658 |
| rs535640268 | snp | A/G | 1.68789e-05 | 0.00290503 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147966838 | TTGAAAACCATGAAA[A/G]GGTAAAATTTTTTTT | 79658 |
| rs535641209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147952452 | TCATTTTAGCCATCG[C/T]AATAGGTATTTGGTA | 79658 |
| rs535642155 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147745337 | TCAAAACATTCAACC[C/G]TGTCTTCAAGCAGGC | 79658 |
| rs535647951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147953676 | TGGCTGGATTGATCA[A/G]TTTTACTGATTATCT | 79658 |
| rs535651004 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147985503 | CAGCGACTCTCCTCT[A/T]ACTTTTGGACCTGTG | 79658 |
| rs535653784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147828850 | AATTTCTATGAATAC[A/G]CATGCCTCACCCTTT | 79658 |
| rs535654692 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147739697 | AGAAGCTGTTTTGAA[A/T]TCTGTGACTTCAATA | 79658 |
| rs535701347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147958723 | TTGGGAAGTGCTTGG[A/G]TGGTTACTGCTAATG | 79658 |
| rs535702239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147966087 | GAGTGATTGTGGGTG[C/T]TCTGACCAAAGTCTG | 79658 |
| rs535706136 | in-del | -/GATGG | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147925850 | TCAGGGCACTGCAAA[-/GATGG]GATGGCCAGGTGATA | 79658 |
| rs535720725 | snp | A/T | 0.00914312 | 0.0669923 | upstream-variant-2KB | ARHGAP10 | GRCh38.p7 | 4:147730876 | ATTAGTGTTTTTTTT[A/T]AAGAAATACTTTTTT | 79658 |
| rs535732826 | snp | G/T | 0.02016 | 0.0983543 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148003614 | TATTGGGTGCATATA[G/T]GTTTAGGATAGTTAG | 79658 |
| rs535737409 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147746141 | ACAGAGTCTCACTCT[G/T]TCGCCAGGCTGGAGT | 79658 |
| rs535737417 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147739199 | CTCAAAAAAAAAAAA[A/G]AAAAGAAAAGAAAAT | 79658 |
| rs535764794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147841662 | GAAAAGGAAATTCTT[A/G]TTGCTCAGTTGACAT | 79658 |
| rs535779724 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147991425 | TTTTTTCCCAGGAGG[A/G]GCCTTACGGAGCTTA | 79658 |
| rs535795995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147752803 | AAGTGCCGGGATTAC[A/G]GGCGTGAGCTGCCGC | 79658 |
| rs535796949 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147918919 | TATTCAATTATTGGG[A/G]CCTTACTCTCTCATA | 79658 |
| rs535813095 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147940462 | TTCATTTCATTACCC[A/C]AGACATTATGTGAAT | 79658 |
| rs535816041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148050683 | CGGTTGATTCATCTT[C/T]TTTCTTATAAAGATT | 79658 |
| rs535829189 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148066763 | GGACTCTGTGCAGCT[A/G]ATTCTTCATCCTAAG | 79658 |
| rs535838854 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147781314 | GTGCCAGAAACTATT[C/G]GGGGATAGGTAGGTG | 79658 |
| rs535843576 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147947433 | TTAAGATGAAGTCTC[A/G]CTCTTTTTGCCCACG | 79658 |
| rs535844262 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148037275 | TGTCCATGACAAACT[A/G]CTGCCCCAGTAGTTT | 79658 |
| rs535844487 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148037714 | GTGGCGTGTGCCTGT[A/G]ATCCCAGCTACTTGG | 79658 |
| rs535846196 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147847901 | CTGAGCTTTGAAATT[A/G]CCCCAGAGAAATAAT | 79658 |
| rs535848627 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148030345 | CTTTGAAACTCTTGT[C/G]GCGTAGGAGGTAGCT | 79658 |
| rs535857941 | snp | A/G | 0.000399281 | 0.0141238 | missense, utr-variant-5-prime, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147822753 | GCCCAGCGGAAGTTT[A/G]CTCATTCACTCAGAG | 79658 |
| rs535860224 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148034237 | TGCTTTCAAATAAAA[C/T]GTAATTTAGTCTTTT | 79658 |
| rs535877441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147900242 | CCTGATTGGTGATAC[C/T]ATGTATTTGTATTTG | 79658 |
| rs535878090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147876462 | GCAGGGCGTAGTGGC[A/G]GGCACCTGTAGTCCC | 79658 |
| rs535885786 | snp | C/T | 1.67307e-05 | 0.00289224 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148046877 | TTTGATATTCAATGC[C/T]TTTTTTCCTCCTAGG | 79658 |
| rs535886745 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148030947 | TCCTATAATCCCAGC[A/G]TGTTGGGTGGCCGAG | 79658 |
| rs535908677 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147906516 | AAGATGATAAATTTT[A/T]GGTTACATGTATTTT | 79658 |
| rs535911599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148036995 | TTGGAAAAAAAACAG[C/T]CTTAGATAATCCAGC | 79658 |
| rs535912467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147830252 | GACCTTTTGCCCCTA[C/T]AGGGAAGGTACTAAG | 79658 |
| rs535922208 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147788978 | GCCATAAACTTATCC[A/G]GTTCTTGCAGCAGCA | 79658 |
| rs535922876 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147821100 | GCTGCGGCAACTATA[C/T]GGGGCCACTGAGCCA | 79658 |
| rs535926851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147813632 | ATGTGACAATTGCAC[A/G]CGACAGAGAAAACTA | 79658 |
| rs535929614 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147750614 | ATCTTTTTTTTTTTT[G/T]GGGGGGGGTTGTAAT | 79658 |
| rs535935938 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147999819 | ACCCCTGCCCTGCCC[C/G]CCTCGTTTACAACAT | 79658 |
| rs535947883 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147919724 | GCTGGGATTACAGGC[A/G]TGTGCCACAATACCC | 79658 |
| rs535948323 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147773617 | TCATTGTTGCCATGA[A/T]GTCATAAGGATTTAA | 79658 |
| rs535956719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148005940 | GAAACAAATACATGT[A/G]TCTCTTAGTGCAGAT | 79658 |
| rs535981953 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147954194 | GGAGTGTCATTTAGG[G/T]GAAGGACATGCCAGT | 79658 |
| rs535985410 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147788403 | AGTGAGCTGAGATCA[C/T]GCCATTGCACTTCAG | 79658 |
| rs535989987 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147747611 | ATGAGTGGAGAAGTT[A/C]TTTGCATGTGTTTCT | 79658 |
| rs535995566 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147794608 | ATTTTTTGGGATTGG[G/T]TTTTGTGTTTTCTGG | 79658 |
| rs536009599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147882613 | CAACATTCATTTGTG[C/T]GTGGGGGGGTTTTCA | 79658 |
| rs536011691 | snp | A/G/T | 5.22774e-05 | 0.00511238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147732500 | GCGGCGTGGCGAGGC[A/G/T]GCTGGGGGAGCCTCT | 79658 |
| rs536017411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148066198 | TGTATCATGGCCACA[C/T]TCTGGCGGAAGGAGG | 79658 |
| rs536029097 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148051398 | TCTTCTATTGTAATT[G/T]ATGGAGCCGGGTCCT | 79658 |
| rs536061553 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148052262 | CCTCCTTCAGAGAGG[G/T]CTTCCTCAACCCCAG | 79658 |
| rs536065659 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147734860 | GGATCTACAGAAAGA[A/G]TAAAACCCACTAGGT | 79658 |
| rs536066691 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148044543 | GACAGTTTGCTATGT[C/G]TAGCTGAGCACTGAG | 79658 |
| rs536066906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147887348 | CTTCTCTCCACTGCT[C/T]CAGGATATTACTCAA | 79658 |
| rs536088589 | in-del | -/TT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147849237 | TTTAAAAGACTCTGC[-/TT]TTTTTTTTTTTTTTA | 79658 |
| rs536091530 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148010429 | GAATAAAACTATCAA[A/C]CTTGTAGGGTTGATC | 79658 |
| rs536093992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147754089 | CTTTCGTCCTCCAGC[A/G]GTGTCTAGAACAGTG | 79658 |
| rs536095129 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147994570 | CATATAAAGAAACAG[A/T]TGACATCAGAAACTC | 79658 |
| rs536095374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147828193 | TAATTGGATATTCAT[A/G]ATTAAGACTGAGTCA | 79658 |
| rs536101303 | in-del | -/GTG | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147840495 | TGGCTGTTTTAAAAT[-/GTG]GTAACCATGCTATTG | 79658 |
| rs536103214 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147834626 | CCTTGTTAGACTTAC[C/G]CCAGAATGGCACTGC | 79658 |
| rs536135651 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147917678 | TCTAGATTAGGTTGT[A/G]TATTTTATAGATGTT | 79658 |
| rs536139803 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148009139 | TTCTCTTTTTTCTCT[C/T]TTTTTTTTTTGAGAT | 79658 |
| rs536140317 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147761280 | CCTTGACCTCTGAAC[A/G]CTCTAGGATTACAGG | 79658 |
| rs536152545 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147760407 | TCTACTTGGCAACGT[C/T]AGGGTTTGAATCCAG | 79658 |
| rs536154635 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147792493 | TATTTGCTTTATTTA[A/T]AATATAATGAACACC | 79658 |
| rs536156980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147826623 | CGAGAGAAATATACA[A/G]TGAAACTACATGGAC | 79658 |
| rs536173755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147856784 | TACTGGACCATTAGG[A/G]AAGATCTTTCCCAAG | 79658 |
| rs536176396 | in-del | -/A | | | upstream-variant-2KB | ARHGAP10 | GRCh38.p7 | 4:147731474 | TACGCAGAGAAGTGT[-/A]AATAGGAGCTGCTGG | 79658 |
| rs536176589 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148009576 | GAATGTAGATGTACA[G/T]AATTTTGATGTTTCC | 79658 |
| rs536186663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147807900 | GTTCATGAAGGTCCT[C/T]GTCCTCCTTTGGTTG | 79658 |
| rs536190415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147880506 | TTTCTGCTTAGTGAT[A/G]TCTTTCTGTTTTAGC | 79658 |
| rs536198245 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148000675 | CATTTCTCTGATGAC[A/C]AGTGATGATGAGCAT | 79658 |
| rs536199828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147929438 | ATGTTATGAATTGCT[A/G]AGTATCTTGGAAGAG | 79658 |
| rs536208694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147775079 | GCCACCACGCCTGGC[C/T]AATTTTTGTATTTTT | 79658 |
| rs536217719 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147734988 | ATTGCCCTGCACGGT[G/T]TCTCCTGTTTGCATT | 79658 |
| rs536218364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147955511 | TAAATGATGTTTGGT[A/G]CCTCCCCTCATCCTT | 79658 |
| rs536220686 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147743016 | TTCTCTGCCATACTG[A/G]TCGATAGTTTTTTTT | 79658 |
| rs536222650 | in-del | -/T | 0.0252325 | 0.109451 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147807441 | TATATTCCAGAATTA[-/T]TTTTTTTTTAAATGT | 79658 |
| rs536227763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147976270 | AAATGCTTCTTGATT[C/T]AGCTTTGCTGGCACT | 79658 |
| rs536242544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147962066 | CTTGATCTCTAAAGC[C/T]TCCTACTGTTTCCAG | 79658 |
| rs536250449 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148055041 | CTTTTCTGTTCAACT[A/G]GCAAGCTAAAGTTCA | 79658 |
| rs536256209 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147741788 | CACACACACACACAC[A/G]CACGCACACACACAC | 79658 |
| rs536263587 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147749250 | TGTTGGCACAGTGAG[G/T]TATCTATGCCTTATA | 79658 |
| rs536265799 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147795973 | GCTGGGATTACAGAC[A/C]TGAGCCATCATGCCC | 79658 |
| rs536294703 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147897534 | TAGTTATGCCTTTTA[A/C]TGTATTTTTTAGATA | 79658 |
| rs536298728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148012825 | CTGTTTTCTTCCTTA[C/T]GATGACAAAATGTTT | 79658 |
| rs536300445 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147755518 | ACAAGAGTGAAACTC[C/T]GTCTCAAAAAAAGGG | 79658 |
| rs536300731 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147756612 | CATCCTGCTCCATCC[C/G]ACCTGGGATGTGAAT | 79658 |
| rs536303919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147829657 | TGTGGTGTGTTGCTG[C/T]CAGAATTCCAGAGAT | 79658 |
| rs536305111 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147961539 | CAGGTATTTAACTTT[A/T]GTCATAAGGAAAACT | 79658 |
| rs536325122 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147947593 | ATTTTAGTAGAGGTG[A/G]GGTTTCGCCATGTTG | 79658 |
| rs536326074 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147977942 | CTCCATTAGTTCACT[C/T]AGGATAACAGCTTTT | 79658 |
| rs536333990 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147849620 | TCTCCTGTTTCCCAT[C/G]TGATAATGTTGTAGC | 79658 |
| rs536336498 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147936383 | CTGGACTGCGGACTG[C/T]AGTGGCGCAATCTCG | 79658 |
| rs536338575 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147844509 | AGCTTCTGGTAACAA[A/C]CCTTCTACTCTCTAT | 79658 |
| rs536369193 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147935846 | TATTTAAATTTCATT[A/T]AAAAATGTAGAAACT | 79658 |
| rs536372716 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147870506 | AAAGGTATTTAAAAG[C/T]GAAAACCTATTTTTC | 79658 |
| rs536374273 | in-del | -/TCAGGAGATTGAGA | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148037623 | GGGCGGATCATGAGG[-/TCAGGAGATTGAGA]TCATCCTGGCCAACA | 79658 |
| rs536374609 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147836182 | CCTAACATACTTGTT[C/T]GTAGAAGATAGATAC | 79658 |
| rs536391531 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148067283 | AAGCCCTTAAGCAGG[G/T]TTTATCTGTGTGTGT | 79658 |
| rs536395160 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148061357 | CTGGGAGATAACTTG[A/G]CAATTGTTTGGCTAA | 79658 |
| rs536418656 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148059754 | AATTAGCCTACCATC[A/G]TTTCCGGGATGCTGG | 79658 |
| rs536433431 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147882040 | GCCTGGGAGAATGTT[A/T]TCTTGCTATATTTCC | 79658 |
| rs536438155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148032773 | GTGCAGCCTTCAGTC[A/G]GTGACCAAAAGCCCG | 79658 |
| rs536442587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147895810 | AAGTGGTGTTATTGG[C/T]CATCTTGCCTTGTTC | 79658 |
| rs536457176 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147808996 | GGATCTCTTGAGCCC[A/G]GGAGTTCCTGGCTGT | 79658 |
| rs536459213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147816457 | CTTCAAGTCATTCAA[A/G]TGACTTCAGATGTGT | 79658 |
| rs536479095 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147902452 | AGAGGTTGAGGCCGG[A/G]CGCAGTGGCTCATGC | 79658 |
| rs536482488 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147843128 | CACCCCTTTTCTCCT[G/T]CTATCACAGGGAAGG | 79658 |
| rs536499261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148039196 | CTTCTTTTATTTAAA[C/T]ACTTAAGGAATTTCT | 79658 |
| rs536500409 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148031957 | AATGAACAAACATCT[C/G]GTCATGGATTGGTTG | 79658 |
| rs536516798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148058232 | ATGAAAGATCATTTC[A/G]CTAATGTGTTAGCTT | 79658 |
| rs536530707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148071430 | AGAGCAGGCTGGCCA[A/G]TGTGGTGAAACCCCA | 79658 |
| rs536531291 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147955664 | CAAGTACTGGGGCAT[A/T]CTTCTCATTATACTA | 79658 |
| rs536544233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147949473 | CATGTTTGGAGACAT[C/T]ACTGATTTTCACCAT | 79658 |
| rs536547106 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147753736 | AAATTATATTTGAGA[C/G]AATGATTTTTTTCCC | 79658 |
| rs536547226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147842463 | TATTTATAACCTACC[C/T]CTACTTTCTGAGCAT | 79658 |
| rs536559358 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148017243 | CTCCAGAATATAGAG[C/T]GAGATGCCTTCCGAA | 79658 |
| rs536570268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147995743 | TTTTTTCATGACGGA[A/G]TCTTGCTCTGTCACC | 79658 |
| rs536587789 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147952934 | TTAATTTTTACATAA[A/G]ATATGAGGTATGAAT | 79658 |
| rs536600072 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147912728 | ATCATAACTCACTGC[A/G]GCCTCTACCTGCTGG | 79658 |
| rs536602538 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147796610 | GCTTAACTGCAAGCT[C/G]CGCCTCCCAGGTTCA | 79658 |
| rs536610557 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147852988 | ATACCACAACACTTT[C/T]AATATTAAATATTGA | 79658 |
| rs536617780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147984482 | TTTCCTTTGACCCAC[A/G]GTGGCCTTTGGAGGC | 79658 |
| rs536625590 | snp | C/G | | | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147781390 | TTACATTGGGCTGGA[C/G]CTGGCAAGCCAGGAT | 79658 |
| rs536629594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147969499 | ACAAGCTTTGAGACA[A/G]TGTTACAGTAGCTCA | 79658 |
| rs536630563 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147749900 | ATGCAAATTAACCTG[C/T]TGATGAACAGCCATG | 79658 |
| rs536637677 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147877036 | GAGCATCATTAGTGT[G/T]TATGCCCAGAGCTGG | 79658 |
| rs536641040 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147803999 | TGTATTTTTAGTTTT[G/T]TTTTTTTTTTTCTTT | 79658 |
| rs536650218 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147984943 | CCTACAGGTCCCCCA[A/G/T]TGGCAGGTCCGAGCA | 79658 |
| rs536663988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147883427 | CAGTGTAACACAAGT[C/T]GAGCATACATCTGTG | 79658 |
| rs536673183 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147764591 | AAGGGTGGAGTGCAG[G/T]GGCGTGATCTCAACT | 79658 |
| rs536678905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147897653 | ATCATCCTTTCGCTC[C/T]CTGTGCTCTTGTTAC | 79658 |
| rs536683197 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147845089 | TGTAATGCTCAAACT[C/G]CTCACCTTCATCCTT | 79658 |
| rs536684134 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147809916 | GAGATTTAGGATAAC[A/G]CTTTTCCAAAAGATA | 79658 |
| rs536694637 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147787298 | ACAGTGAGGGCTCAA[A/T]ATTTGAATGAATAAA | 79658 |
| rs536695760 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147921151 | GTAGATAGTGCAGAT[A/G]CAGCCGAATGATTTT | 79658 |
| rs536698543 | in-del | -/TTTA | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147919107 | GTTTTTATTAAAAAC[-/TTTA]TTTGTGATATTATTG | 79658 |
| rs536714214 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148019147 | TTAGCCTGTTACTTG[A/T]TGTCCTTTTCCAGAG | 79658 |
| rs536735256 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147928576 | GATTAGTTGGTGGCA[A/C/G]ATAATAGCTGTCTGT | 79658 |
| rs536736258 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147996831 | GGTGTCCTTAAGAGG[G/T]ACATGCACAGAGCAA | 79658 |
| rs536737775 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147764042 | TTGGGATTACATGGT[A/G]AACCACCATGCCTGG | 79658 |
| rs536744829 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147860474 | ACAAAACAAAAAAAA[A/C]CAGGAGAAAATTGTG | 79658 |
| rs536746801 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147915828 | GATGAGGACAGCTGG[G/T]GGCACTGGCTCACAC | 79658 |
| rs536748044 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147770361 | GAAACCCTGTCTCTA[C/T]TAAAAATGGAAAAAT | 79658 |
| rs536751689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148012066 | CAATTATTAGCATGT[C/T]GACAGTAATACAGAT | 79658 |
| rs536758567 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147852799 | TCTTGGCTCACTACA[A/G]TCTCCGCCACCCAAG | 79658 |
| rs536758703 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147762943 | CATTTGCTAGGGGTA[A/G]TGAAGGATAACAAAA | 79658 |
| rs536765878 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147754900 | GGAGCTCGAGACCAG[C/T]CTGACCAACATGGTG | 79658 |
| rs536774249 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147990635 | GTCCTTTGCAGCAAC[A/G]TGGATGGAGCTGGAG | 79658 |
| rs536780944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147983470 | GATTATAGGCGTGAG[C/T]CACTGCACTCGGCCT | 79658 |
| rs536781732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147951066 | CATTCTGTATGGGGA[A/G]CTTGTCATTTTTATG | 79658 |
| rs536784405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147859960 | AGTGTGAAGCCCTTA[A/G]TAGGGGGGATGCTTT | 79658 |
| rs536784481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147866037 | GCTGACGTTGGGAAT[A/G]GAGCCTGCTGGGTGT | 79658 |
| rs536795426 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147894809 | ATTTAATTGTTTTGG[C/T]ACCTTCTAAAAAATC | 79658 |
| rs536805120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147989382 | GGTTTTGAGATCAAC[C/T]GGTCTGACCAAAATT | 79658 |
| rs536805810 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147922731 | CATACTACCTCCCAC[A/C]CAGCTTTGTGAGGAT | 79658 |
| rs536813988 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147776796 | CACTGGGACTTGTAT[C/T]GCAGCATGGACTTCA | 79658 |
| rs536820114 | in-del | -/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147865594 | AAAAAAACACTGGAT[-/C]CTCATTCTCAGGATT | 79658 |
| rs536829151 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147760728 | CTAATTCATGTCTTA[C/T]TTCTTCTTTTAGGCT | 79658 |
| rs536829380 | snp | G/T | 0.00119737 | 0.0244387 | downstream-variant-500B | ARHGAP10 | GRCh38.p7 | 4:148073203 | CTCCATCTGGATTAA[G/T]TTCGACGTGGAGGGA | 79658 |
| rs536837592 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147963975 | ATGATCTCATCTAAA[C/G]TGACATCTGCAACAG | 79658 |
| rs536855833 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147825342 | GTCCCAGCTACTTGG[A/G]AGGCTGAGGCAGGAG | 79658 |
| rs536863496 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148015569 | GTCAATTCTAGTTAA[A/G]TTTTCTAGAAAAGAC | 79658 |
| rs536863967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147762408 | AAAGATAATTAGTTT[C/T]AGAAGGTATGGAATT | 79658 |
| rs536869059 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147949203 | TGTGCACTATTGTTA[C/T]TCCTGATTGATAAAG | 79658 |
| rs536869910 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148041108 | ATTAAATTCAACTAA[G/T]ATATTAGATCTTTTC | 79658 |
| rs536895484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147825081 | TTCGTAGGTGTCACT[C/T]TAATTTCCTGGGTGG | 79658 |
| rs536898658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147963438 | GCAGTAAATTTAGAA[C/T]CTAATTCTCTTTTGT | 79658 |
| rs536907594 | in-del | -/TG | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147810886 | ATTGAGCATCTACTC[-/TG]TGCCTCATTTTGTTC | 79658 |
| rs536927093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147915135 | CTGCCACCTATGAAA[C/T]TAGTGTGTAGGATAT | 79658 |
| rs536934517 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147736396 | TTTGGGGAAATTTCT[G/T]AAGTTGCCATTACAT | 79658 |
| rs536936559 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147743665 | GCCTGTAATCCCAGC[A/T]ACTCTGGAGGCTGAG | 79658 |
| rs536969822 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147838276 | CTCAAGCCAAAAGTA[A/T]ATGTTAGCAGCCCAT | 79658 |
| rs536971245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147988492 | ACAGCCTTTTCCTCT[A/G]TCTAGCTCTGAAGCT | 79658 |
| rs536977188 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147863806 | TTATGTTTCAATATT[A/G]TTTTACTTAAAGCAC | 79658 |
| rs536983098 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147955928 | AGGCCTATAGTTGGT[A/T]GAATTTTGTGATTGA | 79658 |
| rs536990734 | snp | A/C | 0.00247627 | 0.0350999 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147948979 | TCAAAAAAAAAAAAA[A/C]AAAAAAACCCCCAAA | 79658 |
| rs536999410 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148014724 | TGATAAAGATTGTCA[A/G]TATGCTGAAACCTTT | 79658 |
| rs537006523 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147980297 | TCTATTGAGATGATC[A/G]TATAGTTTTTGTTTT | 79658 |
| rs537010092 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147778393 | GGGACATAACTTACC[A/G]AGATCTGCCATGACA | 79658 |
| rs537010676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147944107 | ACTTGTATGTTAAAA[C/T]GAGATTTAAATAATT | 79658 |
| rs537010748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147945052 | TTCAGATAGGTTTGC[A/G]ACTCGCTTGTGGTGG | 79658 |
| rs537019477 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147772139 | CTCTCCTGAGAAGTT[C/G]TCTCTACTTCTGCTC | 79658 |
| rs537027529 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148043037 | GCTTCCCAAGACCAA[A/G]ACGTGGTCTGCACCC | 79658 |
| rs537032761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148027262 | GTCTTCTTTTGTAAC[A/G]TGATACAGCAGCTTA | 79658 |
| rs537040763 | snp | G/T | 0.0614824 | 0.164198 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147905529 | CTCAGGTTTGTCAAA[G/T]ATCAGATAGTTGTAG | 79658 |
| rs537062742 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148035561 | CTTCATTATAGTTCC[A/C]ATTTTGTCTTGCCAT | 79658 |
| rs537063323 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148009571 | TGTTAGAATGTAGAT[A/G]TACAGAATTTTGATG | 79658 |
| rs537071479 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148027838 | GCAGGCCACTGTGCG[G/T]TCTTTTTAAATGTAG | 79658 |
| rs537074477 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148020917 | TTTACACTCCCATTT[A/T]CTGGTGTTTTGATTT | 79658 |
| rs537079325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911193 | AGTGAATTCTTGAGC[A/G]GAAAACCACTGCCCA | 79658 |
| rs537089250 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147819042 | AAGCATGCTCTTTAC[A/C]TAGGGAGAAATACAT | 79658 |
| rs537096502 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148024589 | TATATTGCTTAAGAC[A/G]TAGGTACATATGATA | 79658 |
| rs537101559 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147826651 | GACTCGACATCCAGC[C/T]TCAGACCAGTCTCGT | 79658 |
| rs537116362 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147810311 | ATTTTTTGGTGTTTA[C/T]TAGTGATTTCTATTT | 79658 |
| rs537116661 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147910609 | TTCAAATATTCAAGG[A/T]CAACGATCTTCACAT | 79658 |
| rs537124719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147786235 | CTCTTAAGCAGCTGC[A/G]TCATATCCAAGAACT | 79658 |
| rs537148854 | snp | C/T | 3.3942e-05 | 0.00411945 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147909811 | AAATGATTGTATCCT[C/T]CTTTTCCATCTATTA | 79658 |
| rs537171472 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148055075 | CTCTTACCTGATTCC[A/G]CACTGATCATCTGGA | 79658 |
| rs537171878 | in-del | -/AT | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147878452 | CAGCTGCTTACTAGG[-/AT]ATGCTGTTCATGGAC | 79658 |
| rs537172067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148003669 | TACCATTATGTAATG[A/G]CCTTCTTTGTCTCTT | 79658 |
| rs537186208 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147785747 | GACTTTGGCCAATTA[G/T]TGTGGATTTTCAGCA | 79658 |
| rs537188711 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147792360 | CTGCCTATTTATAAC[A/G]TGTCCTCTTCCTTCC | 79658 |
| rs537193951 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148002308 | TGTGCTGCTGGATTC[A/G]GTTTGCCAGTATTTT | 79658 |
| rs537198347 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147879422 | ATGGTTTATATTTTA[A/G]TGGTTTATATTCATG | 79658 |
| rs537200587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147791800 | GTGTTGGCCAGGCTC[A/G]TCTCGAACTCCTGAC | 79658 |
| rs537204475 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147818940 | AAACCCTAAGAGGAG[A/C]TCACCAGAAAGGGGA | 79658 |
| rs537228192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147817427 | AATTGTTGATAAATA[A/G]GTGGCTCTGCTATAA | 79658 |
| rs537229403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147970990 | CCCAGCTATTCAGGA[A/G]GCTGAGGCAGAAGAA | 79658 |
| rs537230908 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148040492 | GATTACAGGCGTGCA[C/T]CACCACACCTGGCTA | 79658 |
| rs537234606 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147878887 | GTTCACACCATTCTC[C/G]TGCCTCAGCCTCCCG | 79658 |
| rs537263191 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147791533 | TTCCGTGTGTGTGTG[C/T]GCGCGCGCGTGCGTG | 79658 |
| rs537264120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147964693 | TGACTAGACCCCATC[A/G]AGTAAACGATGAACA | 79658 |
| rs537267375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147885391 | CCCTTTATAAAAACT[A/G]TCAGATCTTGTGAGA | 79658 |
| rs537293794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147923452 | AAATAGTCATTACCA[C/T]TTAAAACTAAATTTG | 79658 |
| rs537317563 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148006977 | TACTATACTACCTGG[A/C]TAGCTTTTCTTGATT | 79658 |
| rs537329212 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148068872 | AGGGACCTGCCTCTC[G/T]TTGGTGCTACTTGGG | 79658 |
| rs537356893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148001580 | TTGTTTGTGTCCTCT[C/T]TTATTTCATTGAGCA | 79658 |
| rs537362537 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147805978 | GCTAAAAAGAAGCCC[A/G]TGTTTGTACTTATAC | 79658 |
| rs537362654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147756998 | TCTAGGCTGGTGGCA[A/G]TGCAGTTGCAGAGAG | 79658 |
| rs537366436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147796514 | TCTCTTTTTTTCCTT[A/G]TTTCTTTTTTTTTAT | 79658 |
| rs537370133 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147797319 | ACTGACCCCAGCATG[A/C]CTTCTATGTTCCTCA | 79658 |
| rs537385306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147790370 | AATTTTGGGGGAAAC[A/G]CAAACATTCAGTTCG | 79658 |
| rs537390147 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147945256 | TACCAGAATTGACAC[C/T]TTCCATTCCACAATT | 79658 |
| rs537393877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148047835 | CTTTTTTTTTCTTTT[C/T]TTTAAAGATGGAGTT | 79658 |
| rs537413183 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147952560 | TTTATATATTTTCTT[G/T]GGTGAAGTGTCTGTG | 79658 |
| rs537414963 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147883000 | AGTTCAGGTCAGAAC[C/G]CAGGAATACAAAAGT | 79658 |
| rs537420403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147739799 | GGAGTGCAATGGCAT[A/G]ATCTTGGTTCACTGC | 79658 |
| rs537425866 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147867887 | AAAAAAAAAAAAAAA[C/G]TTGAGAGTGAATACC | 79658 |
| rs537448390 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148051474 | TTTAAGAAATATCGG[A/G]CATTGCTATCTGCTT | 79658 |
| rs537471666 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148043496 | TAAAATCTTTATTCC[C/T]AGCCAGGGGTGGTGG | 79658 |
| rs537475192 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147842283 | GTTAGCCTTTGGGGC[A/T]CAGACGGATATTGCA | 79658 |
| rs537478769 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147834708 | CACCCACACCCATAC[A/C]CATACCCACCCACTT | 79658 |
| rs537480275 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147881160 | ACACCTGTAATCCCA[A/G]CTATTTGGGTGGCTG | 79658 |
| rs537487777 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147917850 | AGAGGTCTTAAAGTC[A/G]CATTTATTAAACCAG | 79658 |
| rs537489386 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARHGAP10 | GRCh38.p7 | 4:147730996 | AAGCGATTCTCCTGC[C/T]TCAGCTGGGACTACA | 79658 |
| rs537492696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147926060 | TTCCACCATGCTGGG[A/G]TGGTGTTGGTAGTGG | 79658 |
| rs537497149 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147833817 | GATATATATATTAAG[G/T]TGGTGGTAGAGATTG | 79658 |
| rs537506662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147965217 | ACGGGTGGAACTGGG[A/G]ACCACACCTGGAAGG | 79658 |
| rs537508157 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148015764 | GCTTAAACCTGTAGA[A/C]TCCAAAGCTCAAAGT | 79658 |
| rs537522865 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147916759 | ACATGGTATAGCTGC[C/G]GGGGCATATCTAGAG | 79658 |
| rs537529410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147925352 | CCTTTTCTGATGTTT[C/T]CCATCTCTGCAGCAG | 79658 |
| rs537529944 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147738559 | CTCTGTCTCCCCCCC[A/C]CAAAAAAAATTATAA | 79658 |
| rs537530750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148064285 | TGTTCACTTCCACGT[C/T]AATTTCTCTTTTGGG | 79658 |
| rs537533664 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147933618 | GGACTCAGAAGTTGA[A/C/T]GTGGCTTTCTGCCCC | 79658 |
| rs537560056 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147833290 | CCCCATGCTGTTCTT[A/G]TTATAGTGAGGGAGT | 79658 |
| rs537580837 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148050229 | TTTGTGATATTGATG[G/T]AATTATTAGTGAACA | 79658 |
| rs537604505 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147923386 | CTGTATGATATGCAA[A/G]AACAAAGTAACACTC | 79658 |
| rs537612084 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148063550 | GTCTTTGTGGTGCTG[G/T]TTGTGCATTTATGAA | 79658 |
| rs537618009 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148070178 | TATATATACACGTAT[A/G]CCTGCACACACGCAC | 79658 |
| rs537632240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147798965 | GATTTTTTTCTTTGT[C/T]TTTAGTTTTCAGAAG | 79658 |
| rs537645329 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148049471 | TCCTCCCAGTAGCCG[A/G]TGTGTGCTTCCCACA | 79658 |
| rs537668357 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148047851 | TTTAAAGATGGAGTT[G/T]TGCTTTTGTTGCCCA | 79658 |
| rs537669445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147971787 | CACTCATAGTTTTCA[A/G]GTAAACTGCTTCACA | 79658 |
| rs537670179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147839845 | TAAGATCCTTACATC[C/T]GAATGTCTGACGAAA | 79658 |
| rs537674894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148023059 | GTTGTTTTGATTTAA[A/G]TTTAATCAGAGATTT | 79658 |
| rs537677366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147891555 | TGGTTATGCAATTCT[A/G]TGGATATGTTACAAG | 79658 |
| rs537700702 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147745973 | TTGCATCTTTTTAGT[A/G]GAGATGGGGTTTCAC | 79658 |
| rs537704484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147899097 | GGTGGTCTCTCAGTC[C/T]TGCTCTCAGACTTCC | 79658 |
| rs537715998 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147905861 | TGATTCTTCCTATCC[A/G]TGAGCATGGAATGTT | 79658 |
| rs537723763 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147931119 | AGGAAGATGTGGGTG[A/T]TGTGAGTAGTGCTCT | 79658 |
| rs537748521 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147992248 | GTTCGGTCCCCACAT[A/T]TTTTGGAGAAGCCAG | 79658 |
| rs537748867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147939073 | AAATGGAGATTTTCT[C/T]ACCCTTAATGCTACT | 79658 |
| rs537754062 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147853757 | TTTTTTTTTATATTG[C/G]CAAGTTCTTATGGCT | 79658 |
| rs537764571 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147937909 | ACTTGAACCTGTGAG[A/G/T]TGGAGGTTGCAGTGA | 79658 |
| rs537765563 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147893065 | TGAATGGAAGTAAAT[C/T]TTTTTTTTTTTGAGA | 79658 |
| rs537781345 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147740892 | CCATTCTTTTCCCCA[A/G]GGGGTAGGACCTATC | 79658 |
| rs537783021 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147995802 | GCTCACTGCGAGCTT[C/T]GCCTCCTGGGTTCAC | 79658 |
| rs537783558 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147946012 | TGTTCCCCCAGTGCG[C/T]GTGTGGGCCCTTAGT | 79658 |
| rs537790519 | snp | A/G | | | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147966801 | GACTTGAAGTTTCAG[A/G]ATATTGTTGTGGAAA | 79658 |
| rs537793399 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147787095 | GTGCAGCTCTTCTCA[A/C]TAGTCATATCTCCTC | 79658 |
| rs537808144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147942033 | ATAATCTTAGGGGCA[C/T]TTTTTTCTCCAACTT | 79658 |
| rs537815151 | in-del | -/A | 0.0150606 | 0.0854603 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148052426 | TTGGGCTAATTGACC[-/A]AAATGAACATATACT | 79658 |
| rs537817913 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147792915 | AGCACTTTGGGAGGC[C/T]GAGGCAGGCGGATCA | 79658 |
| rs537819011 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147981136 | CTTGTTTTTCTGGTT[G/T]CTTTAGGTACAAGGT | 79658 |
| rs537823474 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147881369 | ATGGCTGGGCGCGGT[G/T]GCTCACGCCTGTAAT | 79658 |
| rs537830770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147895054 | AAAACCCATAGGTCA[A/G]TATTGTGAATATAGA | 79658 |
| rs537844864 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148031823 | AGCATGGGCCCTCCA[G/T]GAGAAAAATCCAGGC | 79658 |
| rs537856763 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147974045 | TTTCCTTTCTTTTGG[C/G]TATACACCTAGCAGT | 79658 |
| rs537857999 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147746165 | CTGGAGTGCTGTGGC[A/G]TGATCTTGGCTCACT | 79658 |
| rs537858516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147982023 | AAATTCAATTTGCCA[C/T]CCTATGTCTTTTATT | 79658 |
| rs537873668 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147973848 | TTCAGTTCCATCCAT[A/G]CCATTGTAAATGACA | 79658 |
| rs537877175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147761367 | TAAAAATCTTTTCTA[A/G]GTTTTTCTCCTTTTA | 79658 |
| rs537880186 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147753494 | GGCTATAGGTGTGCA[C/G]CACCGTACCTGGCTA | 79658 |
| rs537880635 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147939629 | CATTGTTTGCTGAGA[-/T]TATTTTTTTAACCAC | 79658 |
| rs537881687 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148017371 | AAAGCAACATCAAAT[A/C]ATTATACATCAAATA | 79658 |
| rs537886748 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148009607 | CAGTCTGGAAGCCCT[A/G]TACTGAAAGAAATTA | 79658 |
| rs537894187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147752817 | CAGGCGTGAGCTGCC[A/G]CACCTGGCCTGCTTT | 79658 |
| rs537898261 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147879414 | TCATTTTAATGGTTT[-/A]TATTTTAATGGTTTA | 79658 |
| rs537900392 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147886542 | CTTCCTTAACTAGTT[G/T]AAATTTCATAGTCAC | 79658 |
| rs537902855 | in-del | -/TCT | 0.00716266 | 0.059414 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147770988 | GTATCTTTGTCCTAA[-/TCT]TCTTTTCTTTTAAGG | 79658 |
| rs537916275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147815179 | CTGCCGCCCTTGTCC[A/G]CCTTCAGTCTGCTCT | 79658 |
| rs537918611 | snp | C/T | 0.00517822 | 0.0506191 | upstream-variant-2KB | ARHGAP10 | GRCh38.p7 | 4:147731705 | AGTTATGTCGCCCGC[C/T]TGCGGGGACTAACGA | 79658 |
| rs537922651 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148067018 | CTGGCTGGGGCACCC[C/T]GGGTGTCTCAGGAGC | 79658 |
| rs537946577 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147768285 | GAGTGTCAGGCTGAA[G/T]GAATCATGGAGCTAT | 79658 |
| rs537949138 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147900470 | TGGTTTATTTTTTTC[A/G]TTCATGAAATTTATA | 79658 |
| rs537950299 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147848567 | TCTCTTTAAGCTCTT[C/T]AAAGCTTGTTGCATT | 79658 |
| rs537953772 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147759590 | ACACCGCCCCCCCCC[C/T]CCTTTAAAAAGGAAA | 79658 |
| rs537955940 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147794441 | GTACCACATATATAT[G/T]TGCACTTTTATGAGT | 79658 |
| rs537970699 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147799725 | CAACAGAATTTATAA[A/T]TGATTATTGAAGCAC | 79658 |
| rs537983296 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147863227 | CCCAGACTGCAGCTC[A/T]GTACCTATTAACAAT | 79658 |
| rs538005523 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147939621 | ACATGGAACATTGTT[G/T]GCTGAGATTATTTTT | 79658 |
| rs538009115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147733917 | TGCTTGAATCAGAAA[C/T]GGGACTCTGGGACAT | 79658 |
| rs538019335 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147954848 | GGAATAAAGATAAAT[G/T]CTTATTTTTATAATA | 79658 |
| rs538021363 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147862487 | TGCCTGTTTCTGGCC[A/C]CCGCGGGCACCATGG | 79658 |
| rs538025090 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148045517 | GAGGCTGAGGCAGGC[A/G]GATCACCTGAGGTCA | 79658 |
| rs538026358 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147947550 | TGGGATTACAGGCTT[G/T]CACCACCACGCCTGG | 79658 |
| rs538030104 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147881599 | GCCAAGATCCTGCCA[C/T]TGCACTCCAGCCTGG | 79658 |
| rs538038053 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147738225 | TTGCTCAAGCTGCTT[A/T]GCTTTTCTATATCTG | 79658 |
| rs538039886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147892282 | TGCATGATGCTGTAC[C/T]GTTTCTCAATTTAAA | 79658 |
| rs538041277 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147979427 | TCCTATTTTTGTGCC[C/G]ATACTATGCTGTTTT | 79658 |
| rs538041380 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147961375 | GGTCTTTTGCCCTTT[G/T]GTCTGTTGGATTGTC | 79658 |
| rs538066682 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147875735 | TAAAAGATATTCCTA[C/T]GTGGCATCCTAACTT | 79658 |
| rs538089158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147829480 | AGATGTGAGCCACCG[C/T]GCCCGGCCAGGACAG | 79658 |
| rs538090599 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147874412 | GGGTTTCAGAAATGT[A/G]ATTTGTCTCTTCAGA | 79658 |
| rs538132365 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147999308 | AAACCCAGGCATTTG[A/C]GCCATCAATGGCTAC | 79658 |
| rs538141770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147740134 | GCTCACTGCAACCTC[C/T]GCCTCCCAGGTTCAA | 79658 |
| rs538148809 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147772629 | CGCCCAGGGAATTCC[A/G]AACAAAAACAGATGA | 79658 |
| rs538162127 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147828410 | CTCTATGCTTAAATA[C/G]GCTGTATTAAGTATA | 79658 |
| rs538165768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147835559 | TTGTATTTTTAGTAG[A/G]GACAGGGTTTCACCA | 79658 |
| rs538196840 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148044745 | AGAAAAGAACTGGAC[A/G]GAGTTGAGCTCGCTG | 79658 |
| rs538197175 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147749356 | AAGAAAATATTTAAA[G/T]AATTAAATAGCAGTT | 79658 |
| rs538199406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147934527 | GGAGTTGTGACTAAG[A/G]TTGTGGACTTGTTTT | 79658 |
| rs538204593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147850198 | ACCAATCAGCACTCT[A/G]TAAAAATGGACCAAT | 79658 |
| rs538229736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147864388 | TCCCTGAGCGCTGAG[A/G]TGCTGGGCCCTTTCT | 79658 |
| rs538231786 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147816538 | GAGTTAGGGCCAGGA[A/T]TGCTTTACCAGAATA | 79658 |
| rs538238918 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147902503 | GAGGCCGAGGTGGGC[C/T]GATCACCTTGTCAGG | 79658 |
| rs538242371 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147801373 | CTCTATAAGAAAAGA[C/G]AAGAGAACCATTGCT | 79658 |
| rs538244454 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147808043 | ATAATTATTTCTTAC[A/G]TGTCTTTTTGTGGTC | 79658 |
| rs538260807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147901619 | AAGACATATAATACT[A/G]CTTTACTTTTTACGC | 79658 |
| rs538270198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148040252 | GGGCTTCTCCCAGTC[C/T]CTATTTCCACATGAA | 79658 |
| rs538281578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147908720 | AAATATTGGTGAAAA[C/T]ATGAGCTCCATCTTA | 79658 |
| rs538292697 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147823769 | CTCAAAAAAAAAGAA[A/G]AAACAAAACAAAAAA | 79658 |
| rs538297577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148031003 | AGTTGAGGCTGCAGC[A/G]AGCCGTGATTATACC | 79658 |
| rs538320289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147962326 | TAATAATAGTAACAC[A/G]AACAACAACAGTACT | 79658 |
| rs538332667 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148000705 | TTTTTTCATGTGTCT[G/T]TTGGCTGCATAAATG | 79658 |
| rs538334047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147994059 | TTATTCATTTATAGC[C/T]TGACTTCTTCCAAAA | 79658 |
| rs538341295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148006383 | CGAAAATGGTGGGAA[C/T]GTCAAATATATGACC | 79658 |
| rs538349154 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147871975 | GGAGGTGGTGGCACA[C/T]GTGAGTAGTCCCTGT | 79658 |
| rs538360885 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147733328 | TGATGCTACTGGAAA[A/G]TGGGGCGGAATTAGC | 79658 |
| rs538360905 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147980393 | GAATAAAGCCTACTT[C/G]ATCATGGCAAATTAA | 79658 |
| rs538403918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148000197 | TTTTTTTGTCCTTGC[A/G]ATAGTTTGCTGAGAA | 79658 |
| rs538405814 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147780577 | AAAAAAGACTGAACT[C/G]TATTATCAGTGCAGG | 79658 |
| rs538409210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147814417 | TTTCTCATTTGTGCC[A/G]TGAATGTTGTTACTC | 79658 |
| rs538416921 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148069604 | GTGTGGTGTGTATAG[G/T]GTAGGAGGAGAAATA | 79658 |
| rs538447595 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148037792 | GTGAGCCAAGATCAC[A/G]CCACTGCTCTCCAGC | 79658 |
| rs538470322 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147821149 | GCCGGCGAGCCTGGG[A/C]TTGTTCTCGTGAAGG | 79658 |
| rs538480698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147795128 | CACTGTGTCACCTAC[A/G]CTGGAGTGTAGTTAC | 79658 |
| rs538502457 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911652 | CAGGCGTGAGCCACC[A/G]CGCCTGGCCTCTTAA | 79658 |
| rs538524884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148004812 | GACCTCCAGAGCAGA[A/G]GACACAGTTTAGCTG | 79658 |
| rs538524923 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148009088 | GAAGTTCTTTGGGGG[-/A]AAAAAAACAAAAAAG | 79658 |
| rs538540309 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147950170 | TAAGATGGCAGATGC[C/T]TTGGGAGATTTGAAA | 79658 |
| rs538546357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147843750 | TCAAACTCCTGACCT[C/T]AGGTGATCCACCTGC | 79658 |
| rs538560467 | snp | A/C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148041766 | ATGTCCTCTTGACCA[A/C/G]TTGTGGTCAGTTTTT | 79658 |
| rs538561843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147754124 | GCTCATAGGCACTGA[A/G]TCAGTACCCATCTGG | 79658 |
| rs538563553 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147818507 | GGAGGCGGAGTTTGC[A/G]GTGAGCTGAGATCTT | 79658 |
| rs538563659 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147762242 | TGAACCCCTGGCCTC[A/G]AGCAGTCTGCCTTCC | 79658 |
| rs538578376 | snp | C/T | 4.96882e-05 | 0.00498414 | stop-gained, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147875102 | CCCAAGGACCACAAA[C/T]GAGCAAGTCAGTTTA | 79658 |
| rs538579559 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147787830 | CATGATGCCTGGGGG[G/T]AAGACAGCAGCAGCG | 79658 |
| rs538582485 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148050819 | GTCTTTTCCCCCTTT[A/G]TCTCTGCATACCAGC | 79658 |
| rs538590087 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147846847 | AAGTGTTCTGTTAAT[C/G]AATGTGATAGACCCC | 79658 |
| rs538597227 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147888085 | ACTTGCTTCAAGGAC[A/G]TCACACTCCCTCTCG | 79658 |
| rs538603083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147979267 | GTTTCATTCTGCTGC[A/G]TAGAGTTAGCCAGTT | 79658 |
| rs538608293 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147956896 | TTGAAATTTGAATAT[C/T]AGTGTGTTTTACCAA | 79658 |
| rs538610080 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147897180 | TTTTATAAACAGCAT[A/G]TACTTGAGTTCTGTT | 79658 |
| rs538644392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148055779 | GGCTGGCTCCCTGCT[A/G]CTTGAGAGATGATCT | 79658 |
| rs538645054 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147956226 | TCATTTCCTTTTATT[G/T]TCTCCTCTTGGATGT | 79658 |
| rs538656490 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148025147 | ATTTAGCATATCTCT[C/T]ATGGGAACACTCAAG | 79658 |
| rs538664316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147743888 | ATTGCCTGAACCATA[A/G]TGAACTCTCTCTGTG | 79658 |
| rs538672455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147797281 | CTCCAGATGAAGATC[C/T]AACCTCTTAGCCAGG | 79658 |
| rs538676593 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147964050 | CTGATGTTTTGACAT[C/T]TGGGGCCTCACTGAC | 79658 |
| rs538677870 | snp | G/T | 1.64991e-05 | 0.00287215 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147822936 | TTTTTTGAAGAATCT[G/T]GAGGAACAGAGAGAA | 79658 |
| rs538687275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147735859 | AAATAACCAGTGTCT[C/T]CTTTAAATGCAGTTT | 79658 |
| rs538696752 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147922803 | CCTATCTTCATTTCC[G/T]TCTTCATCCTTCTCC | 79658 |
| rs538707405 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148033666 | TTTCAGCTTAACTCC[G/T]AAGCAAGCTGTGTTT | 79658 |
| rs538712631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147742638 | ATAGGCACCTGCCAC[C/T]ACGCCTGGCTAATTT | 79658 |
| rs538715085 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148020547 | AACATGCGTTTTTTG[G/T]TTTTTTTTTTATTCC | 79658 |
| rs538723690 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147735115 | CTTACTGCTGAATTC[A/T]ATTAGGTAGCAATCT | 79658 |
| rs538735036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147913705 | TGAGAAACTGGTGTT[C/T]AGGGCTTCTACATAA | 79658 |
| rs538736851 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147871765 | CATTCTATTGATTTT[A/T]TGCAAAGTTTTCAAT | 79658 |
| rs538753198 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147822577 | CCAGGTTGAAGATGG[C/T]GGGCCATTTGGCAAG | 79658 |
| rs538778048 | snp | C/T | 0.000197945 | 0.00994651 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148046907 | GTGACAATCCTTACC[C/T]TTCCAAGGAGGACAC | 79658 |
| rs538792896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147796671 | GCTGGGATCACAGGC[A/G]CCTGCCACCATGCCC | 79658 |
| rs538793593 | in-del | -/GTGG | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147755780 | GAAAGAAGGTGGGGT[-/GTGG]GTGGGTGTGTGTGAG | 79658 |
| rs538800860 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147998603 | GCAAATAGAATCAAT[A/T]CTTTATAACATTGCA | 79658 |
| rs538806652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147968667 | TTCTTTCAAGAACTT[C/T]TAGATTTTTTTTTCT | 79658 |
| rs538813747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147936453 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 79658 |
| rs538838417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148026264 | TTCAGTTCAGCATCA[A/G]GCAGATCAAAAAAGC | 79658 |
| rs538845389 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147962178 | GCTGTGTTTCTGTCT[G/T]TTGGTGGAATTGGCC | 79658 |
| rs538848902 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147753621 | AGCCTCCCAGAGTGC[G/T]GGGATTACAGGCGTG | 79658 |
| rs538857039 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148058010 | ACTGCTGTTGTCCCT[C/T]GGTGTGCTCGTGGGG | 79658 |
| rs538861838 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147836707 | GAGCTATTGCCATCA[A/T]AAAATTGAATTTCGT | 79658 |
| rs538867053 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147847359 | GAAATGTGCTTTTCC[C/T]CCTTTGGGGGATATG | 79658 |
| rs538878472 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148019815 | TAACCTAACCTTCCA[G/T]AGCTGTTAAGATTTA | 79658 |
| rs538903163 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148009829 | TGAAATTGCCTTTGG[-/C]CCTTTGAGTCGAGTT | 79658 |
| rs538903405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148018131 | GTTTTTCTTATGTTG[C/T]AAATACGTAGGTGCT | 79658 |
| rs538912593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147809591 | TGGTCACTGGTGACA[C/T]GGGTTTGTGAGCCCC | 79658 |
| rs538914595 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148033338 | TTCCAGCCATCCTGG[G/T]ATGATAAAGATTTGT | 79658 |
| rs538920114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147747662 | GTTTTTTTGTGGAAA[A/G]GATAGAGTTTAAAAA | 79658 |
| rs538921689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147927764 | CTTGATCCTAAGGGA[A/G]GGCGCAGAGGCTGTG | 79658 |
| rs538946201 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147996159 | CTTCCACAAAGGTAC[A/T]GTCTCCTCCTGATTG | 79658 |
| rs538955203 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147763076 | CCATAATAAAACTGT[A/G]TAAGATTTATTGCAA | 79658 |
| rs538959840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147801957 | AACTCTTTGGATGTC[C/T]GGGATGGGAGGCATT | 79658 |
| rs538960615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147794707 | CCCATTGCCATTGAG[C/T]ATTCCATTATCTCCA | 79658 |
| rs538961130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147943498 | GTCAGTGTTGAGTAG[A/G]GTGCTAGCAGCTGCA | 79658 |
| rs538973249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148060642 | TCATCTCCATAGACA[C/T]TGTCTCCAGCCTTGC | 79658 |
| rs538985469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147791286 | CTGGCTAATTTTTGT[A/G]TTTTTAGCAGAGACA | 79658 |
| rs538993730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147744524 | TCGGAGTGCAGTTGT[A/G]CAAATGAATCGGAGG | 79658 |
| rs538994628 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147783486 | TATAATTTATATAGC[A/G]CACATTAAATTATGT | 79658 |
| rs539000271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147990071 | ACTCCTGATATTCAG[C/T]CTTCTGCCTGAATGA | 79658 |
| rs539003139 | in-del | -/ATATA | 0.0115144 | 0.0749975 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147784398 | TATAATTTATAAATT[-/ATATA]ATATAAAGTTATATA | 79658 |
| rs539003404 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147937131 | CTGGTGCCAAAAAGG[G/T]TGGGGATGGGGGCTG | 79658 |
| rs539005835 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147963505 | CAACAACAAACATTT[A/T]ATTGATTTATTTGAT | 79658 |
| rs539009600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147854270 | CACCATAAAAATCAT[C/T]GGATTTTTCAGCAGT | 79658 |
| rs539015701 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147977802 | TCCACCCTTTCTCTC[C/T]CTCTCCCCCTCCCCC | 79658 |
| rs539017019 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147970431 | AATGGATGGCGGTGG[C/G]GGGAGGGTGCAAAAA | 79658 |
| rs539022905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147931202 | TTTGATTTTACCTTA[C/T]CCATTTTGCCCAGAG | 79658 |
| rs539028209 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147884739 | CATGTGGAGGCCTGG[A/T]GACAGGAGAGAGCAT | 79658 |
| rs539048788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147839018 | AGACTCTTAAGAACT[C/T]TTACACGAGGCAAGT | 79658 |
| rs539067385 | snp | C/T | | | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147864892 | ACTTCTATGAACTGT[C/T]TCTCGAGTATGTGTG | 79658 |
| rs539076063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148063686 | GTGGCCAAGTCCATA[A/G]AGGACAGAGCTGCTG | 79658 |
| rs539076352 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147757700 | AGCTTCACCTTCCAC[A/G]ACTGCACACCTGGGT | 79658 |
| rs539076933 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147750647 | CACTCTGTAACCCAG[C/G]CTGGAGTGCAGTGGC | 79658 |
| rs539086248 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147966286 | TTCAACCAGCTACTG[A/G]TCAAAAATCCAGTAT | 79658 |
| rs539103925 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147904071 | CATTTTGCATTGCCA[C/G]CAGCAATGAATAAGA | 79658 |
| rs539106493 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147801612 | TGGCCTTATAAAATG[C/T]TTCTTGCAAAAGAAA | 79658 |
| rs539121949 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147853854 | GGCTTCATTGTTTAC[A/T]TGTGACTCTTTCAAT | 79658 |
| rs539140394 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147910854 | AGCCAGTGTTTGAAT[A/G]AAACACAACTCTTGT | 79658 |
| rs539142079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147945906 | ACCAGCGGGCTCCCA[C/T]CTCTCATATTGAACG | 79658 |
| rs539142230 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147938780 | CTGTCAGCCAGTTGT[G/T]TTCTTGTTACCTTTA | 79658 |
| rs539143299 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147937130 | CCTGGTGCCAAAAAG[G/T]TTGGGGATGGGGGCT | 79658 |
| rs539163852 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889989 | CGAGCATAGTTTACT[A/T]TTATCAGTCACCTGA | 79658 |
| rs539172035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148055152 | GAGATGTAATTCTGC[A/G]CCTGTTCTCTTACAG | 79658 |
| rs539179259 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147945290 | TAACTCTCCCATCTC[A/C]TTTTTTTTTTCCTGG | 79658 |
| rs539182603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147977015 | CATGTTCATGTTAGG[A/G]ATGGGATTGAGGTGG | 79658 |
| rs539186107 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147946986 | CACTATGAAACAACT[C/T]GTCGAGGCTGATGAT | 79658 |
| rs539197260 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147957302 | CAATGTAGACTTTAA[A/G]TTTTTATTTTAATCT | 79658 |
| rs539199050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147852151 | ACCTTGCCAAACAGG[A/G]GTTGCTCAGCTTTTT | 79658 |
| rs539214530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147951805 | CACAGTTGACATACA[A/G]TAAGCTGCATATATT | 79658 |
| rs539214888 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147783601 | AGAACACATTAAATT[A/G]TGTATTGTATAATTT | 79658 |
| rs539228934 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147771110 | GCACTTTGGGAGGCC[C/G]AGGTTGGAAGATCAC | 79658 |
| rs539230172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147984265 | CCCAGTACACATTCG[C/T]GTTCAGCGGCTGGAG | 79658 |
| rs539232413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148055645 | ATGAGCCAAGATTGC[A/G]CCACTGCACTCCAGC | 79658 |
| rs539237076 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147811212 | CACCCAAGTCAGACT[A/C/G]GTAAGTGCGGGCCCC | 79658 |
| rs539243968 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147976527 | GCTATGAAAACTTTA[C/T]TGTTTTGTGTGTGGT | 79658 |
| rs539247007 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148042206 | CCTAAGCCATGAACC[C/T]GAGGCTCATCTTAAG | 79658 |
| rs539248096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148068004 | CCCCACCCTCGGGAG[A/G]GGGCTGTGTTTGTAA | 79658 |
| rs539253372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147951142 | GCCTAGCTAGACATA[C/T]GGCAATGATATAAGT | 79658 |
| rs539267030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147755582 | GAAGAAAGAGAGGGC[C/T]GTTTTGGAAAACACT | 79658 |
| rs539274528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147895899 | TGTAGATGCCCTTTT[C/T]ATTTTGAGGAAGTTT | 79658 |
| rs539291148 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147826531 | GGTGGCAGCCACAGC[A/C]AACCACGGAATTAAC | 79658 |
| rs539309342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148041325 | GTGGAAGAACAGCAG[A/G]GAAGGGATTTCAGGG | 79658 |
| rs539309427 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148049280 | GAGAGCTTGCCATTC[C/T]AAGGAGTTCCCAGGT | 79658 |
| rs539314568 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147936046 | CGTTTTCACAGAGGC[A/G]TGTTTGCTTGAATGC | 79658 |
| rs539315093 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147851383 | ATGCATGGCTAATTT[G/T]AAAATTATTTTTGTA | 79658 |
| rs539318337 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147989475 | TTCACCTCTGCAATC[A/T]TGACCATAAGAGACA | 79658 |
| rs539338664 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147859837 | AGAAACATGAAGAGA[A/T]CCTAACGATGAATAA | 79658 |
| rs539355518 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147865256 | TATCTTTTAAAAATT[C/T]CTCTGAAATAATTTA | 79658 |
| rs539360093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147862298 | GGCGCCGGGAGCCGG[A/G]AGAGGCCAGGGAGCA | 79658 |
| rs539371763 | snp | A/C | 1.64749e-05 | 0.00287005 | missense, intron-variant, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148063230 | AACTCAGCTGTGACA[A/C]CTCTTTCACCCGGGT | 79658 |
| rs539373091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147950224 | TATGTTATTTTTAGC[A/G]ATGGAAAATGCAGTA | 79658 |
| rs539374504 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147746284 | AATTTTTGTATTTTT[A/G]GTAGAGACGAGGTTT | 79658 |
| rs539376026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147938844 | GAAAGCTGCAACTCA[C/T]TTGAGAAGTAAATAT | 79658 |
| rs539380904 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148057994 | GCCTTTGTTTCTCTG[A/C]ACTGCTGTTGTCCCT | 79658 |
| rs539394099 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147985447 | CAGGCCACCAAGCTG[G/T]CTCTGTCTGCACGCC | 79658 |
| rs539394619 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147957706 | CCCTCCCTGCTGAGA[G/T]TTCTCAAGGTTTCTC | 79658 |
| rs539400238 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147891251 | TTAAGAGATGAATGG[A/G]TAAATAAAAGGTGGT | 79658 |
| rs539405797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147992685 | TGCTGGGATTACAGA[C/T]GTGAGCCATTGCACC | 79658 |
| rs539409959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148028657 | GAGAAGAGTTGTAAC[A/G]TTTTGAAAATAATAC | 79658 |
| rs539430958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147805369 | TGCTGTTTCGGTTAC[C/T]GTAGCCATGTTGTAC | 79658 |
| rs539432976 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148021685 | CCACAACCTTCTTAC[A/G]TCTGAACAATGACAG | 79658 |
| rs539437982 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147899422 | TTCATTCATTAGGTC[G/T]TTTTTACATCTTTGC | 79658 |
| rs539438920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147798063 | GTGTTTCTTAAGTGG[C/T]AGATGAATAGTTCCT | 79658 |
| rs539447859 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148036001 | AAAGGTTTCATTTTA[A/T]TGTCAAACTTAGTAT | 79658 |
| rs539465669 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147774108 | TAGTTGTGATAATGA[A/C]ATGAGTTAATAAATG | 79658 |
| rs539469135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148022087 | ACCCTCACTTGTATC[A/G]AAGGTTGTGTACCAC | 79658 |
| rs539471988 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148035451 | TTCTTGAGAAGTCAC[A/G]TTTTTCTTTTTCTAG | 79658 |
| rs539492917 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147732145 | CGCCGCAGGACTCGG[C/T]TCTACGGGACATGTC | 79658 |
| rs539497519 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147749353 | GCCAAGAAAATATTT[A/T]AAGAATTAAATAGCA | 79658 |
| rs539499889 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147959763 | TTCTTAATCCAGGTT[C/T]TGACTCTATTTTTCA | 79658 |
| rs539529428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147772916 | GAGTCATTGGGTGGG[C/T]GGAACTGATTAGAAT | 79658 |
| rs539531746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147739585 | ACAATAAAAGAAGAC[A/G]ACCAGAGACATCCCT | 79658 |
| rs539538832 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147791670 | GCTCCCTGTAACTTC[C/T]GCCTCCTGGGTTCCA | 79658 |
| rs539556838 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147881055 | GAGGTGGGCAGATCA[C/G]TTGAGGTCAGGAGTT | 79658 |
| rs539560868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911370 | AATTTTTGTTGTTGT[C/T]GTTGTTGTTGGAGAC | 79658 |
| rs539572302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147866580 | TTACTTGAATATTAG[C/T]GACTTCCCTTTAATC | 79658 |
| rs539573351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147874384 | TGACAGATATTGGCA[C/T]ACCAAGTGTCCTGGG | 79658 |
| rs539576658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147867993 | AACCTTATTTTTATA[A/G]TTTATGTGTCAACTT | 79658 |
| rs539577902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147990748 | GGACACAAAAAGGGA[A/G]CAACAGACGCCGAGG | 79658 |
| rs539593500 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147778590 | TGTAGTAAATATGCA[C/T]GTGTTCTCTCCCTCA | 79658 |
| rs539597552 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148044711 | AGGCCAGCCCCTCGC[A/G]TCACTTGGGCTCTTT | 79658 |
| rs539602093 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147997697 | AAAGAATAACTTAAC[C/G]TGGTCAAAGAATCCA | 79658 |
| rs539617182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148034106 | GCCTGGAACAACTGA[A/G]TTAATGGATGTAAAC | 79658 |
| rs539627048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147958225 | CAAAGTCCTTGCTGT[A/G]TCATTTTGATAAGAG | 79658 |
| rs539634249 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148032788 | GGTGACCAAAAGCCC[A/G]AAAGCCCACTGGTGT | 79658 |
| rs539652483 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147884196 | GTCTCTGGTTTTCTC[A/T]GAGACCTTGATCATG | 79658 |
| rs539653133 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147745638 | CTGGGACTACAGGCG[C/T]CCACAACCACGCCCT | 79658 |
| rs539654270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147910388 | ACTTTCTCTACATTT[A/G]CTTTAATGTTTATTA | 79658 |
| rs539665691 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147959120 | ACTTTTTTTGGAGTA[C/G]CTTAAAGGTATTATG | 79658 |
| rs539676380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147964572 | CTGCGAGTTCTAAGG[A/G]CTAGAACTTCAACAT | 79658 |
| rs539690082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148059258 | TTCTTCTGTCTTGGT[A/G]AACGTGGTTTCTGAG | 79658 |
| rs539698159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148007754 | TCCCAGTTTTAACCT[C/T]TGGGGTCAAATACAA | 79658 |
| rs539699742 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147752122 | TCTCCTAACCTCATG[A/T]TCTGCCTGCCTTGGC | 79658 |
| rs539708431 | snp | A/G | | | upstream-variant-2KB | ARHGAP10 | GRCh38.p7 | 4:147730902 | TTTTTTTTTTTTTGA[A/G]ACATTGTCTCGCTCT | 79658 |
| rs539729734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148002393 | TTTTGTTGTCTCTCT[A/G]CCAGGCTTTGGTATC | 79658 |
| rs539729889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147777281 | TTTTTTTTTTTTAGA[C/T]GGAGTCTCACTCTGT | 79658 |
| rs539739440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147745315 | TTTGGCCTGCCATCC[A/G]AATACTTCAAAACAT | 79658 |
| rs539744948 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147847665 | TGTAATTTCCTTCAA[G/T]TTAACAAAAATTTAT | 79658 |
| rs539745844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147839947 | TTTGAATTGTGAAGT[C/T]CTAATGGATTCTCTA | 79658 |
| rs539750240 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148008493 | GGTGGTACTGCTGGT[A/G]TGTATCTAGTAGGTA | 79658 |
| rs539757044 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148021301 | ACCCTCACTTCAAAC[C/T]GGAGGAAAGAGGTGG | 79658 |
| rs539763036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147751604 | CTCCTGGCCTCAAGT[A/G]ATGTGCCTACCTCCG | 79658 |
| rs539770483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147872564 | TGCGTGTAACTTTTG[A/G]CTTCCCCCAAATTTG | 79658 |
| rs539771348 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148064145 | TAGGAAAGGGCATCC[C/T]ACCAGGTAGGGAGGA | 79658 |
| rs539788207 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147927446 | GTCAATACAGAATCT[A/G]CATATGACAATATAT | 79658 |
| rs539824146 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147954371 | TCAAGTGTTTTGGGG[A/C]TCTCTTATTAGATCT | 79658 |
| rs539825375 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148036401 | TTCCTATAATCCCCA[C/T]GTGTCGTGGGAAGGA | 79658 |
| rs539825550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147821185 | GGGTTCCATGAGAGT[A/G]GAGCAGAGGTGTGTA | 79658 |
| rs539832207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147960734 | GCCCTTTCTCTTGCT[C/T]ATGTGGTCATTATCC | 79658 |
| rs539840077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148044299 | TAAACCCCTGGTCTC[C/T]AGTTCCCCAAAGTTG | 79658 |
| rs539847299 | in-del | -/A | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147742157 | GTGGAATGGTCTCTT[-/A]AAAAAAAAAATGAGT | 79658 |
| rs539848210 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147953580 | TTTATTTTTAATATC[A/T]TTAGAATCTGCACTG | 79658 |
| rs539851115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147732659 | GGCGAGTCCCCATTC[C/T]CGCCCCTGCGGCTCT | 79658 |
| rs539857559 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147906023 | ATTCACTCATGATTT[C/G]GCTCTCTTTGTCTAT | 79658 |
| rs539862113 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148037200 | GGGGCAGTAAGAAAT[C/G]ATAAGCTGTTCTGGA | 79658 |
| rs539877113 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148036839 | CTGCTCTGTGTGTAC[C/G/T]GGTCATTCCATGTAT | 79658 |
| rs539895369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147819746 | GTATTTCTAGTAGAG[A/G]TGGGGTTTCACCGTG | 79658 |
| rs539905071 | in-del | -/GGTC | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148037093 | TAACTTTGGGGATCT[-/GGTC]GGTCACCCAGTTTCT | 79658 |
| rs539910198 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147868779 | ATCTAGATCCACGTG[C/T]GCAGTTCACAATACG | 79658 |
| rs539913220 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148049588 | CACCTCCGGGAAGTC[C/T]TCCCCATGCTGTAAT | 79658 |
| rs539945611 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147739829 | CAACCTCCGCCTCCC[A/G]GGTTCAAGCGATTCT | 79658 |
| rs539948710 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147763412 | CGCCTCCTGGGTTCA[A/G]GCGATTCTCCTGCCT | 79658 |
| rs539955422 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147827468 | TGGGCAGCCCCTAAG[C/G]TTGTGGCTGTTAGGA | 79658 |
| rs539959697 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147791348 | AACTCCTAGCCTCAG[A/G]TGATCTGCCTGCCTC | 79658 |
| rs539974867 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147770705 | TTCAGATTCCACCTC[C/T]GCTACATACTGGCTT | 79658 |
| rs539985833 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147787246 | AGTATTTATTTATTT[A/T]TTTTTTCTTTTCCTT | 79658 |
| rs539990563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147925364 | TTTCCCATCTCTGCA[A/G]CAGAGGAATGAAAAG | 79658 |
| rs539992993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147739123 | ATCCAGGAGACGGAG[A/G]TTGCAGTGAGCTGAG | 79658 |
| rs539995815 | in-del | -/GG | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148049488 | GTGTGCTTCCCACAT[-/GG]TCTGGTTCTCTTTGC | 79658 |
| rs539998399 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148051579 | TCAGAATAGCTCACT[C/G]TAGCTGGGGGTGCCG | 79658 |
| rs540004107 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147982499 | CATGTCAGCTTCCTA[A/G]GACTGTAGCTGGGAC | 79658 |
| rs540033109 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147880779 | ATGGTTCTAGCTTTA[C/G]ATTATGAAAATATTT | 79658 |
| rs540035360 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147793409 | AAGAACAGAATTTCA[C/G]AGCAATATCTTAGGA | 79658 |
| rs540045598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147966015 | CCTGAATTAAGTTGC[A/G]GGGCTGCTGAGAACA | 79658 |
| rs540051679 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147833873 | TGTAGTGGGAAAATA[C/T]GGTTTCGAAGCTGTG | 79658 |
| rs540063095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148050668 | GTGAGCCACCGTGCC[C/T]GGTTGATTCATCTTC | 79658 |
| rs540063158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148043080 | CAAGGGAAATGGGCA[C/T]CTAAAACCAGGTTAT | 79658 |
| rs540086123 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147925216 | CCTCAGAAGCCAAAC[A/T]AACACCACAAAACAC | 79658 |
| rs540106159 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148015135 | GCAGCAGGACTCCAA[A/G]CAGGGCCCTTCATTT | 79658 |
| rs540107353 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147799123 | CACTGCAACCTCTGC[C/G]TCCCGGGTTCAAGCG | 79658 |
| rs540107629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148015355 | CTGCCACTGACTAGT[A/G]GTATGAATATGAGCA | 79658 |
| rs540107792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148023104 | CTGTTAAAAAAATAA[A/G]AGGCTATGACCTCTT | 79658 |
| rs540109089 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147752442 | AAATTGAAAAAAACG[C/G]TATTGTTTGCTTTTA | 79658 |
| rs540112765 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147964232 | TGCCCTTGTCACTTC[A/G]GTTCCGAGTATCAGC | 79658 |
| rs540116637 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147840459 | ATTCTGGTTACATTC[A/C]TGCTTTACCCCAGTT | 79658 |
| rs540132955 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147835417 | TTGCTCTGTCGCCCA[G/T]GCTGGAGTGCAGTGG | 79658 |
| rs540143627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148015825 | TTAGAAAGAAGATCG[A/G]ACATTTTATTTCTGT | 79658 |
| rs540156426 | in-del | -/A | 0.273856 | 0.248859 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148052340 | TTAATCTGATTATGT[-/A]AAAAAAAAAAAAAAA | 79658 |
| rs540184544 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148017244 | TCCAGAATATAGAGC[A/G]AGATGCCTTCCGAAA | 79658 |
| rs540188874 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147992940 | AGAAAGTAAGAAACT[G/T]ATTGGAGGGTGTATT | 79658 |
| rs540190902 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147999978 | CATGTGCACAACGTG[C/T]GGGTTTGTTACATAT | 79658 |
| rs540195682 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147788526 | TTTTGTTTGTCCAGT[C/T]CTTGGTGAGATTAGG | 79658 |
| rs540196985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147773711 | ACCAAAAGCCTTAAA[A/G]TGGAATGATAGGGAA | 79658 |
| rs540234463 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147980725 | CATTACTCCATTATC[A/G]GTCTGTTCAGGATTT | 79658 |
| rs540237612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147868907 | TAACAGGCCATGGAC[C/T]GGTACCTGTCGGCAG | 79658 |
| rs540238190 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147953851 | GGTACAAAATGAAGT[C/G]CTTGGTTTACCACCC | 79658 |
| rs540244952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147968722 | TGCTAATAACATTCC[C/T]GACTTCTGCCTCTAA | 79658 |
| rs540252691 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147947835 | TGAAAAATTTCAGAT[A/G]CATAAGATGAGAGTT | 79658 |
| rs540253564 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147779625 | ACATTTCCTTCAGTT[G/T]GGGAGTCTGGGGAGT | 79658 |
| rs540261515 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147906248 | TCCATGTTCATAGCA[A/G]CACTGTTCACAACAG | 79658 |
| rs540275418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148053478 | CCTTGGCTGAGATGC[A/G]GGCGGGAGGGCCTTC | 79658 |
| rs540282043 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147746998 | TGAGTGGGATGGCAT[A/G]CAGATGTTAAGCTGA | 79658 |
| rs540296099 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148062682 | AGAGGAAGCCTGAAT[C/T]CAGTGGCATTTTCTT | 79658 |
| rs540303594 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148004377 | CTTTTGAAAAGAATG[A/C]ATAGATTTAAATAGT | 79658 |
| rs540304747 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147836268 | TGAGAGAGCCAGGTC[A/G]TAGGCAGATATTCAG | 79658 |
| rs540313487 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147862890 | AGATGTGCCAACTAA[C/T]TGCTGATGGCTGAAC | 79658 |
| rs540317546 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147953035 | ATTGTCTATTGATAT[C/G]ATCATACAGTTTTCT | 79658 |
| rs540326957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147843337 | TCTCTTTCAGCAGTC[A/G]TCCTCTCTCTCTACT | 79658 |
| rs540350953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147739494 | GATACTTTTTGAGGA[C/T]GTGAACTCAAAATTA | 79658 |
| rs540363423 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147778775 | TTGCAGTGTTATCCT[C/T]TTGCTCCATTTCATT | 79658 |
| rs540363882 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147974181 | TTCTCTACATCCTTG[C/G/T]CAACATTTTTTATTG | 79658 |
| rs540364616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148059142 | GTGATGTTGGCCTTC[C/T]GTGCTGAAGATAGAG | 79658 |
| rs540371160 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147960196 | CCCTTTAGACAGTTG[C/T]GTTTTTGTTTCTGGT | 79658 |
| rs540394794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147941337 | TCAAAATTTGTTGGT[C/T]ATCTCATAAAATTCT | 79658 |
| rs540394904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148071571 | CAGTGAGCCGAGATC[A/G]CGCCACCGCACTCCA | 79658 |
| rs540396856 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148064796 | AAGAAGCTAGTGTCA[A/C]TTGGACTTAAGAAAT | 79658 |
| rs540402422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147934547 | GGACTTGTTTTAAGA[C/T]GTACCCTGGTGGGTG | 79658 |
| rs540403785 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147965596 | TTAAGTATAGAGATC[A/C]TTCTAACTGTAGAAT | 79658 |
| rs540405055 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148065125 | CTTATGGCTCAGTGT[A/C]TTTTTTCTCCTGCTC | 79658 |
| rs540407906 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147874167 | GCCCCTTTTATTGTA[C/G]GGAGGAAAGAGGAGA | 79658 |
| rs540408603 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147924847 | AATGCTTAGGACATT[A/G]GCACCTGTTGAATAG | 79658 |
| rs540423480 | snp | A/C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148031205 | AGTGATTATTTAAGT[A/C/T]TGTTTATTATCTTGG | 79658 |
| rs540427639 | snp | A/G | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147940727 | TTCCAACCTGTCTGC[A/G]TCTTAAAACATTACA | 79658 |
| rs540429375 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147973407 | TTTAATTTTCGTGGG[C/T]ACATAGTTGGTGTAT | 79658 |
| rs540431122 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147987977 | TGGTTGCAACCAAAT[A/C]ATCTCTCCAGCAGTG | 79658 |
| rs540449837 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147745749 | GCCCGCCTCGGCCTC[C/T]CAAAGTGCTGGGATT | 79658 |
| rs540453863 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147926597 | GAAAGCAAGAGGAGA[A/G]ATGGCAGGAATTATT | 79658 |
| rs540457128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147834340 | GTGTGGTGGTGGCAC[A/G]CATCTGTAGGCCCAG | 79658 |
| rs540465296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148009366 | CCAACTCCTGACCTC[A/G]AGTGATCTGCCCACC | 79658 |
| rs540475620 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147793442 | TGAACTTGCATCAGA[A/G]TGAGAAACAAAATGC | 79658 |
| rs540510637 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147881721 | TTGAAAGAGGATAGG[A/G]TAAAGAGAAGGACTT | 79658 |
| rs540514896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148040793 | AGGGAAGTTATGTAT[C/T]TTTATTTATTAAAAA | 79658 |
| rs540518228 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147874901 | GGTATTTTGAGAAAT[C/T]TATAAAAAAGTTATT | 79658 |
| rs540518570 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147978961 | TTCTGGAAATTAGTT[C/T]TTTGTCAGATGCATA | 79658 |
| rs540532341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148071024 | GCACCATGCCCAGAT[A/G]TATAAGGCTCAGGCT | 79658 |
| rs540532502 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147857143 | AGGTGTGAGCCACTG[A/G]CCTATTATTCCATTT | 79658 |
| rs540539620 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148067708 | GCCACCCAGTGGCCT[C/T]TGGAGAAAACAAACT | 79658 |
| rs540541200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147814557 | GTAACTTGTCTTGAC[A/G]TTACTCCCACATGTG | 79658 |
| rs540542033 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147751849 | ATCTAGGTAGCTGAG[G/T]CTCCTGCAAGTTATA | 79658 |
| rs540551020 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147932344 | GTTTTATTATAAAGA[C/T]GCATGCATATGTTCA | 79658 |
| rs540560552 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148034439 | TCTCCTGCCTCAGCT[G/T]CCTGAGTAGCTGGGA | 79658 |
| rs540570241 | snp | A/G | 1.64841e-05 | 0.00287085 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147906642 | GTGTCTTTCAGGCCT[A/G]GCGTTTCCTTGACCA | 79658 |
| rs540570932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147855631 | TGAGGCAGTTAAAGA[A/G]AAGTCCCTGATCTTT | 79658 |
| rs540574626 | snp | G/T | 1.69997e-05 | 0.0029154 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148064388 | TCCACATTTTCATTG[G/T]TGTCTTTTGTATTCT | 79658 |
| rs540575496 | in-del | -/A | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147814818 | GGCCCATTCTTAATG[-/A]CCTCATTTTAACTGA | 79658 |
| rs540578369 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147920340 | GAGAATGGTGTGAAC[C/T]CGGGAGGTGGAGCTT | 79658 |
| rs540584090 | in-del | -/C | 0.00795532 | 0.062565 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147751527 | TGCTACCACGCCTGG[-/C]CATTTTTTTTGTATT | 79658 |
| rs540590674 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148052588 | AATAAGATGAGCAGC[G/T]TTACTCTGTTTACTT | 79658 |
| rs540621968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889076 | ACATTTAACAGATTT[A/G]TACTGGATTAAACGA | 79658 |
| rs540634228 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147936174 | TCTGGATGTGCCCTT[C/G]TGGCTTCCAAAAAGA | 79658 |
| rs540634475 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147983218 | TGAAGCAGAGTCTCA[C/T]TCTGTCGCCCAGGCT | 79658 |
| rs540639764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147740720 | CATTCCTTGTCCTAC[C/T]CTTCAGTAGAGTAAC | 79658 |
| rs540643627 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147861149 | CCAGGCACGGAGTGG[C/T]GAGGAGTTCGTGAGT | 79658 |
| rs540670959 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148025590 | TTTATATTTTACATA[G/T]TCTAAAAAAAAAAGA | 79658 |
| rs540675790 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147755006 | AGAATTGCTTGAACC[C/G]AGGAAATGGAGGTTG | 79658 |
| rs540682709 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147881763 | CCTTGCTCCCCTGCT[C/T]TCCAGTATAGAATGG | 79658 |
| rs540697282 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147900638 | AAATGGCAGTGTTCT[C/G]AGCTGAACCAGTAGA | 79658 |
| rs540700331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147801473 | CAGAATACAGGAAAA[A/G]AATCCAGTGTTCAAT | 79658 |
| rs540715883 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147895180 | TTTTTTTTGGTGTTA[A/C]ATTTTCCTAAATATT | 79658 |
| rs540740452 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148010679 | ACATGGTCACAATAC[A/T]GTTATCTATATATCA | 79658 |
| rs540741896 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148025723 | GAAGAAGATGTATTC[C/T]TGTCATTACGACTTA | 79658 |
| rs540743815 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147996987 | AATTTCTGTTGTTAC[C/G]CTGTCTGTGGTATTC | 79658 |
| rs540753315 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148059893 | AATGCAGCTTGGGCC[A/G]GGTCACACCTACATG | 79658 |
| rs540756500 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147989554 | TCCCTTTCTCAGGGA[C/T]GTTCCATGCTGAGAA | 79658 |
| rs540761032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147794269 | TTGTGTTGTCAGCAT[C/T]AGGAGGATTATAAGA | 79658 |
| rs540780286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147901977 | GCCGACTTTGAGAGT[A/G]TAAGTATATGTAAGT | 79658 |
| rs540780766 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147778376 | CTACAACTCTTTAAC[C/T]TGGGACATAACTTAC | 79658 |
| rs540784116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147934188 | GACCCCTTGGCAGAT[A/G]GTTTCAACTGCAGGC | 79658 |
| rs540785545 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147872340 | TCTTACTGTCTGGGA[A/G]AAAATTCACAAATTT | 79658 |
| rs540786202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147980582 | GGATTCCCTCCTCTA[C/T]TTTTTGGAATTGTTC | 79658 |
| rs540798852 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147858117 | GCATCTGTTTTACTT[G/T]TATTAATAGACTCAT | 79658 |
| rs540803043 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148022610 | GGAGCAGCACATTTT[A/T]ATTAATGTTGTTATT | 79658 |
| rs540818341 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147894325 | GAGATGTTGAGCACT[A/T]CTTCCTGTGCTTATT | 79658 |
| rs540818903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147887110 | AATATTTTATATTTT[C/T]CTCTCTCTCTTAAGC | 79658 |
| rs540820753 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148023618 | TTTGTCTTTGTTATG[C/G]ATGGTTCTTTTTTTA | 79658 |
| rs540821418 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148013039 | AAATTGTAATTTGGG[-/A]AAAAAATGTTTATCA | 79658 |
| rs540824256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147800805 | TGTGCCTTGTCATTC[A/G]TTATTTTTTTCCTTT | 79658 |
| rs540837549 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147864090 | AAATTAGCTAAGTTA[A/G]GAAAAATATCACATG | 79658 |
| rs540839828 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147779802 | GTCTGTAATGTTTAA[A/G]CTTTTCATGATTCTA | 79658 |
| rs540850347 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147775192 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGCACC | 79658 |
| rs540856502 | in-del | -/A | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147887862 | GCGAGACTCCATCTC[-/A]AAAAAAAAAAAAATT | 79658 |
| rs540860547 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147840364 | AAGACAGCTTTCATG[G/T]TTCCACTAAATGTTC | 79658 |
| rs540865259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147893525 | TAATAAGAATATATA[C/T]ATTTCAGTAAATATA | 79658 |
| rs540882592 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147955694 | ACAAAATGTACAATA[A/T]TGGCATGAGCAAAAT | 79658 |
| rs540892217 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147806717 | CAGCATATTATCTTT[C/T]TTGAGACAAGATGTC | 79658 |
| rs540894511 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148003167 | CTGCCTTCATTTCGT[C/T]ATGTACCCAGTAGTC | 79658 |
| rs540899232 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147807597 | TACCTAAAAATAGAG[A/C]GTTCAAAAGCATAAT | 79658 |
| rs540907367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147908081 | ACTCCTGACCTCAAA[C/T]GATCCACCCACCTTG | 79658 |
| rs540909612 | snp | A/C | | | intron-variant, utr-variant-5-prime | ARHGAP10 | GRCh38.p7 | 4:147854697 | AAATCATATGAGCAC[A/C]AAGAAACAATAATAC | 79658 |
| rs540909832 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147945291 | AACTCTCCCATCTCC[-/T]TTTTTTTTTCCTGGT | 79658 |
| rs540920287 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147993471 | TGTATACAATTATTA[A/T]TTTATTCAGCAAACA | 79658 |
| rs540922423 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147848320 | ATTGAGGCTCAGACC[C/G]TGTGAACAGTGGGAG | 79658 |
| rs540944488 | in-del | -/GTG/GTGG | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147765337 | GGTGTGTGTGTGTGT[-/GTG/GTGG]GGGGGGGGGGGTGTG | 79658 |
| rs540949714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147987282 | AGCTTCTATAATCAT[A/G]TAGCCATTTACATCA | 79658 |
| rs540960330 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147734315 | AGCAGCCAGTGCATC[G/T]GGGGGGCCAGATGTC | 79658 |
| rs540968960 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147870642 | AAGAAAGCAGCAAGA[G/T]GGCTTTTAGGAAATG | 79658 |
| rs540968961 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147876549 | AGTGAGCCAAGATCG[C/T]GCCACTGCACTCCAG | 79658 |
| rs540970559 | in-del | -/TTTTTT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147830530 | TTTTTTTTTTTTTTT[-/TTTTTT]GATGGGGGGAGCCTT | 79658 |
| rs540973005 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147883615 | ATTTCCCCAAGGTCA[C/T]GTAGCTAGTGGGTAG | 79658 |
| rs540975179 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147973644 | ATTCTATCTAACTGT[A/G]TTTTTGTGCCCATTA | 79658 |
| rs540977615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147774265 | TTTGTTCCACATTCC[C/T]GACCTAATTTGTCTT | 79658 |
| rs540996210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148066923 | TAGTGTGCCATAGAC[A/G]AGGCTACGCTTTGAG | 79658 |
| rs540996583 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147763298 | AATGGTGGTGTTTGT[A/T]GTAGGAGTAGATAAT | 79658 |
| rs540998099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147851421 | TCTCTCTGTGTTGCC[C/T]AGGCTGGTCTTGAAC | 79658 |
| rs541001320 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147781087 | GGCGGGGCCGGGCAA[G/T]GTGATTCACGCCTGT | 79658 |
| rs541010038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148041479 | AGTGAAATGACCAGA[A/G]AATGAATGAAGAGAA | 79658 |
| rs541016954 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147803010 | TCCCTTAGTTTTGTT[C/T]ATTGCTTTTTTTTTT | 79658 |
| rs541023121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147935400 | TCTTTTTAGGGATTC[C/T]GTAATAAATGTGTGT | 79658 |
| rs541028784 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147943102 | TCAATTACAATAGTT[C/G]ATGGTAGATTAGAAC | 79658 |
| rs541037951 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147799588 | TTTTTTTATCCTGTC[A/G]TTTTCATCCTACTAT | 79658 |
| rs541048665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148034155 | TATTGAATAGTTTTC[A/G]CTTATATTTTCTTGA | 79658 |
| rs541050308 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147810607 | CAGGCTCAGCTGGAG[A/G]ATGTGTTGGGCCTGA | 79658 |
| rs541075414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147817797 | TTATCCACCAATATA[C/T]AACAGCCTTGAGGGT | 79658 |
| rs541080683 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148024872 | TGAAATAAGCAAATG[G/T]TGGAAAGTAGGAAAG | 79658 |
| rs541092966 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148026302 | AAGAGTCAGCAAGCC[C/T]GTTAGCATGTGTCAC | 79658 |
| rs541094805 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147758475 | TAGAACATATTCATC[A/G]CCCCAGAAAGAAAGC | 79658 |
| rs541094872 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147902586 | TCTCTACTAAAAATA[C/G]AAAAATTAGCTGGGT | 79658 |
| rs541110416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147850777 | TGCCTGATGCATCAC[A/G]TCAAGAGTTTCTCTA | 79658 |
| rs541112950 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147859205 | CAGAGGTCAGTTTAT[A/T]AAAAGTTTTTCCTGA | 79658 |
| rs541113775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147903412 | CCCCATTATCAACAC[C/T]CCCACCAGAATGCTG | 79658 |
| rs541115095 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B | ARHGAP10 | GRCh38.p7 | 4:148072866 | CTACGATGGGGACTC[A/G]TCTCTCTCTGCTGTT | 79658 |
| rs541124006 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147779632 | CTTCAGTTTGGGAGT[C/G]TGGGGAGTGGTGATC | 79658 |
| rs541144495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147909498 | TAAACTCACATGTGA[C/T]CAAAAGGATCTTGTT | 79658 |
| rs541144735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147915244 | CCCACATTCTCTTAC[A/G]GTGGCAATTCACACT | 79658 |
| rs541152813 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147824552 | AAGAGGTTTAATTGA[C/T]TCACAGTTCCGCATT | 79658 |
| rs541167840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147942460 | AGTTTATAATGATTT[C/T]TAAAAGGGTATATGC | 79658 |
| rs541167888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147949697 | TTGACCAAGAGACGT[A/G]CTGCCACTCTAGGAG | 79658 |
| rs541183519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147922194 | GATACATTTGGGACC[C/T]GAGGGCCATCAGGCA | 79658 |
| rs541191097 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147810527 | ATTAACCATCTGAAC[A/G]TTTACATCTCATCTT | 79658 |
| rs541192106 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147736614 | ATTCCTTTTCCCCTC[A/T]GACAATCCAGATTTC | 79658 |
| rs541201120 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147816991 | TCAGCAGACCTTTGC[A/G]TAGTTGATAATCTAA | 79658 |
| rs541202730 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147949163 | TGTTTTCAGCCACTG[A/T]TCTAAATTTTTTCTG | 79658 |
| rs541208242 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147776363 | TAGCTGGAATTACAG[A/G]AACGCGTCACCACAC | 79658 |
| rs541208801 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147816034 | TTTTATCTGGTTTTC[A/C]TGTTCCTACTGTAAA | 79658 |
| rs541210844 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148038739 | GAATTCAGGCACAAG[A/G]GGATATAGGGGCATG | 79658 |
| rs541215936 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147957182 | TAATCATTGGCATGG[A/T]TTTGCACCTAAGTGC | 79658 |
| rs541220182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147782621 | CTAAATGCAGCATGC[C/T]AGTCCTGAGATGCAG | 79658 |
| rs541226704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147735177 | ACTGGAATTAGATAC[A/G]GATTTATAATGGGGT | 79658 |
| rs541226750 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147863475 | TATACATATGGATTG[G/T]CTACATTTTATTTAC | 79658 |
| rs541234301 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148055404 | CAAAAGATATTTGTT[A/C]TCAGCTGGGCGCGGT | 79658 |
| rs541244816 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148032238 | TGCGTCTGCAAGCCA[C/G]ATCTGTAGCCATTGA | 79658 |
| rs541247601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148039475 | TTTTTTTTCTTTGTA[C/T]TTTTAGTAAAGACGA | 79658 |
| rs541256537 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148008300 | TCTCCCCCAGTTTCA[C/T]GTCCTCTGCTGATGA | 79658 |
| rs541266759 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148056400 | AGAAGGCTTTTAGTG[C/T]TTCAGTGACTGAAAA | 79658 |
| rs541270516 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148048194 | TAGATAATGGTGTCA[A/T]CTGACCCTAGCTGGG | 79658 |
| rs541271810 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147776890 | GGACTTTCGTTAGGA[C/T]GATAGTACTATGGTA | 79658 |
| rs541272071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147815479 | GCCGGAGGCGGGGGG[C/T]GGGGGGAGGAGGTTA | 79658 |
| rs541272152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147823098 | AAAGATGAGGTTTCC[A/G]GAGCCCTGATTTCTA | 79658 |
| rs541284283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147822495 | GGTAGGGGAGGGAAT[A/G]AACATTTTTTCAGCA | 79658 |
| rs541295063 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147831118 | GTGATTCTGAAGCAG[G/T]CTGAAATCAGAGCTA | 79658 |
| rs541298126 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148000348 | ACATTGGGGTTGGTT[C/G]CAAGTCTTTGCTATT | 79658 |
| rs541319161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147921254 | TTGAAGTGTTAGTTT[A/G]GGTAATGAAGGATGT | 79658 |
| rs541355323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147796378 | ATTTTTTTTAAAAGC[A/G]TAGTGGAAGGAGACA | 79658 |
| rs541383613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148046610 | TCCGTATAGTGAGGA[A/G]GTCATTGTGGCTGCC | 79658 |
| rs541391108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147928925 | AACCCAGTTCCCATC[A/G]TTAACCCCATTTTCA | 79658 |
| rs541392268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148057649 | TTCAGCATTAGCTCC[A/G]CACAGATGCTGCCTC | 79658 |
| rs541392667 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147951357 | CCCCTAAAGACTTAC[A/T]TCTGATTGGCCCTTC | 79658 |
| rs541401977 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147770538 | TCAAAGAAATGGTAG[C/G]CTGTATCACATTGTT | 79658 |
| rs541402440 | snp | A/G | 8.34411e-05 | 0.00645861 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147965026 | TTTTTTTTGGAAGAA[A/G]GCGGCAGCCCAGAAT | 79658 |
| rs541404195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147866155 | TCTTTTTACTTCTAG[A/G]TTTATTGACTTACAT | 79658 |
| rs541426878 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147960782 | TCACTCTCCTGACAT[C/T]GTAGGTTGAGGCTGC | 79658 |
| rs541427520 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148022421 | GGTTGATATCTCTAA[C/T]GTATTTTACTTTATG | 79658 |
| rs541429296 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147957810 | GGGTTCATGATACAA[A/C]TATAAATTTCATTTC | 79658 |
| rs541429946 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148049891 | GAGGGTGGGGAAGAC[A/T]GAGTCTCACTCTGTC | 79658 |
| rs541437391 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147738279 | TTGTAGGGCTGGGCG[C/T]GGTGGCTCACGGCTA | 79658 |
| rs541438987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147745374 | CTGCTTAGCATCTGA[A/G]ATCAGACAGGGTTGA | 79658 |
| rs541464667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148042609 | CTGACACTGGTAACT[C/T]TGAAAACTCCTTTTT | 79658 |
| rs541474944 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147958520 | TCGTTTTTGATAAAC[A/G]TATCTGGGAAGCAAG | 79658 |
| rs541475944 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147744826 | CTTTTATGGGTGTGT[A/T]TTTCAGGAATGGGGA | 79658 |
| rs541479128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147785411 | TTGAGAACTTTAGGC[A/G]TAAGTGAAAGCTGTA | 79658 |
| rs541493025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147776978 | TGCAGTGACATTGAC[A/G]CTCTGGAGATAAGTG | 79658 |
| rs541501343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148003338 | CTTTACTTCCAACTA[C/T]GTGGTCAGTTTTGGA | 79658 |
| rs541504928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147737086 | GTTAAATGACATAAG[A/G]CAGTTTTGAGTTGGG | 79658 |
| rs541506840 | snp | C/T | 0.000399281 | 0.0141238 | missense, intron-variant, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148063264 | CCCCTTTCCCCTTTT[C/T]TCCTCCTGCTACTGT | 79658 |
| rs541517579 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148065414 | ATAGATTTCTATATG[C/T]GTGTGATATGTACTC | 79658 |
| rs541520949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147840218 | TTCATTATAGTTCTC[C/T]TGAGTCCCTATGATA | 79658 |
| rs541526951 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148072599 | GGGAAGCAGAGACGC[A/G]CGTCTCAAGCCTGCC | 79658 |
| rs541533261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147831878 | CTGTCTCCTTCTTGG[A/G]CCCCTTTCCCTGCAA | 79658 |
| rs541556574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147832797 | TCTCTTTGTAAGACA[C/T]AATATTTTTCCTTCC | 79658 |
| rs541558923 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147751675 | CCTGGCCTTTTTTTG[A/C]TTTTTTTGGAGCACT | 79658 |
| rs541565519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147743970 | AACCTTATTTATGAC[A/G]GTGGTGGAGTGGTGT | 79658 |
| rs541588600 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147938070 | TTTGCTGGGACATGG[A/C]TGGAAGTGGAGGCCA | 79658 |
| rs541589261 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147923097 | TCAACAATTTCTAAA[A/G]TTATTGGAAGAATTT | 79658 |
| rs541594743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148062781 | GGTCATGTGCTTGAT[A/G]CTAGATTCCTGTGGT | 79658 |
| rs541601784 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147933694 | GAATACTGGCCAAGA[A/C]CTGAGTCCAGAAGAC | 79658 |
| rs541602575 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147779927 | TTTCCCTAGACACTT[A/G]CACCCTTATAGTCTT | 79658 |
| rs541614565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147970125 | TGGCTCTTTGTTCCT[A/G]CTCAGTTGGACTTCA | 79658 |
| rs541622398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147871838 | GGGGATGGTGGCTCA[C/T]GCCTATAATCCCAGC | 79658 |
| rs541624275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147977325 | CTCCAGGGAAGGCAC[C/T]ATCAGGTGCCTTTTC | 79658 |
| rs541627203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147970815 | GATGTAGACTGAGCA[C/T]GGTGGCTCATGCCTG | 79658 |
| rs541633766 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147884256 | ATGATCCTAGCTATG[A/T]TTGGAACCACTCTCC | 79658 |
| rs541642261 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147838482 | GTCTCTTAAAAAAAA[A/C]ACACACACACACACA | 79658 |
| rs541651153 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148022868 | TTGGAAAAAATTGAG[G/T]CCAACGTTTTGGTGT | 79658 |
| rs541657090 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147963549 | AGAACACAATAAAGG[G/T]AATTGGGGTACACTG | 79658 |
| rs541657293 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148021053 | AAGATGTAAACCAAA[A/G]AAAACAAAACAGACT | 79658 |
| rs541660735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147743129 | ACCTCTGCCTCCTGG[A/G]TTCAAGCGATTCTCC | 79658 |
| rs541685812 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148019968 | GACCAGAAGTGTTAT[G/T]AATTTCAATTTTTTT | 79658 |
| rs541704993 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148055595 | TCGGGAGGCGAAGCA[C/T]GAGAATTGCTTGAAC | 79658 |
| rs541712790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148006650 | TTCCTATTGACTTCC[A/G]GAAGAGAGTACTTTT | 79658 |
| rs541720669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147755718 | CTTGCCCTTATATAG[C/T]GTAGGTGATATTTTT | 79658 |
| rs541727509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148061555 | ATAAAATAGATTTTA[C/T]GACTCCCAGATGAAT | 79658 |
| rs541733873 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148015554 | CTGTCAGACCCTGTC[A/G]TCAATTCTAGTTAAA | 79658 |
| rs541743809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147749597 | TTTAATTTTAAATTT[A/G]AAATCAATTGAGAAA | 79658 |
| rs541744499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147756587 | TGAGTAGTGTGATGG[A/G]ATCATGTGCCATCCT | 79658 |
| rs541749363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147976710 | TTTCTTTAGCTGTGG[C/T]ATTGGAAGCTTCTGC | 79658 |
| rs541761313 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147944628 | TTAAAAAGGAAATGC[C/T]AACAAGATGTTGCCT | 79658 |
| rs541773436 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147918187 | GTGGCCTAGGCTGGA[A/G]TGCAGTGGCTTGATC | 79658 |
| rs541780488 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147746318 | CATGTTGGCCAGGAT[A/G]GTCTTGATCTCTTAA | 79658 |
| rs541784529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147969758 | GGCAAGCCTGTTACA[A/G]TAGTTACAGCAGACG | 79658 |
| rs541784756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147748884 | GGATTGCTTGAATCC[A/G]GGAGATTGATGCTGC | 79658 |
| rs541789184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147984680 | CAGGAGACTAACCTC[A/G]TTCCTGAGTGCTGTG | 79658 |
| rs541811871 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147849155 | AGTAGAGAAAGGTGG[A/T]TGTCTGTGTTCTGTA | 79658 |
| rs541813000 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147930352 | ACTGATTAATCATCA[A/G]TATATTAATTGTTCA | 79658 |
| rs541826073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147848684 | TGCTATATGTGTGAC[A/G]GTTATATTATGGAAA | 79658 |
| rs541829238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147879059 | ACAGGCGTGAGCCAC[C/T]GTGCCCGGCCTCCCC | 79658 |
| rs541833567 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147771190 | TCTCTGTTTAAACAG[A/G]AAAAAAGAATCCCGT | 79658 |
| rs541848547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147799999 | AGTCTTAGCACACAG[A/G]TCCTGCCCTACATTT | 79658 |
| rs541853007 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147886399 | TTAGACTTTGTCATT[A/G]CAAGGAACTGCAGTC | 79658 |
| rs541858561 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148035348 | TTTAATTTATAGTTC[A/T]GGAGTTGCCTTTTTA | 79658 |
| rs541885087 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147759923 | CTGGCTAATTTTTGT[A/G]TTTTTTAGTAGAGAC | 79658 |
| rs541894897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148008582 | ACTTAGCAGTCCCCA[A/G]ATGCTAATAGTGCTG | 79658 |
| rs541907993 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148042376 | ATATGCCTTTACATT[A/G]GATACAAAGTTCTTT | 79658 |
| rs541910035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148022552 | ATATGCTTTCTTTGT[A/G]GCACAAATTGCTTTT | 79658 |
| rs541910114 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147992709 | TTGCACCTGGCCGAA[A/G]AAGCCTTTTAATAAA | 79658 |
| rs541920868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147751110 | CTTGAACCCGGAAGG[C/T]AGAGGTTGCAGTGAG | 79658 |
| rs541921502 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148014506 | GTTCACCTGATATAG[A/T]TGGGGAGAAAGTTTA | 79658 |
| rs541922541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147766176 | GTGTCTGTAGTCCCA[A/G]CTACTCAGGAGCCTG | 79658 |
| rs541937579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147931283 | GTTTGCTAACTATCA[A/G]AACGAATCTCAATCT | 79658 |
| rs541940269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147855282 | CTGACACCTAATTCA[A/G]TGTGTACTTCACAGC | 79658 |
| rs541949661 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147903196 | CCAGCAGGCTCATGG[C/T]GCCAGTGAGGAGGCT | 79658 |
| rs541949733 | in-del | -/CTGT | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148069551 | CCTCCTCTGTTCATC[-/CTGT]CTTTTATTAATACCG | 79658 |
| rs541956659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148069867 | TGCATAGAATCCAAA[A/G]CTTTTCCCTGATGGT | 79658 |
| rs541958142 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148008024 | CTGGATGTGCCCTGT[A/G]TTTGTTAATCCTGTC | 79658 |
| rs541959616 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147786494 | TCCGCTTTTTCATTG[A/T]TCTCTTTCCCTTAAC | 79658 |
| rs541971447 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147992428 | TTTAATTTTTTTTGT[G/T]GAGGAGTCTCGCTCT | 79658 |
| rs541974731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147791554 | CGCGTGCGTGCGCGC[A/G]TGTATATATATATAT | 79658 |
| rs541974903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147798172 | GATACATTCTTTCAG[C/T]AGCTTTATTTAAATG | 79658 |
| rs541982219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147757276 | CTGGGCTCACTGCAA[C/T]CTCTGCCTCCCGTGT | 79658 |
| rs541984183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147765671 | TGGGTGTGGTGGCAC[A/G]TGCCTGTTGTCCGAG | 79658 |
| rs541989591 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147979085 | TTGTCTGTTTTTGAT[A/T]TTGTTGCATTTGCTT | 79658 |
| rs542005036 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148028016 | GCCACATACGGTTTT[C/T]CCTTTAAAGGAGCTA | 79658 |
| rs542013519 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147985060 | AGTTCTCTGCATGAG[G/T]CAGTGGAGCTGCCTA | 79658 |
| rs542017032 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147804112 | CCAGGTAATAAGCAT[A/G]GTACCCAATAGGTAG | 79658 |
| rs542024124 | in-del | -/TGTT | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148039779 | TTTTCCTTACTCCTC[-/TGTT]TGGCACTCTCAGTCC | 79658 |
| rs542025017 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147868212 | CCTGCAGGTAGTAGA[A/G]TATTGAGTCTAATGT | 79658 |
| rs542037993 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147797594 | AATTTTGTATTTTTA[A/C/G]TAGAGACGGGGTTTC | 79658 |
| rs542045425 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147853048 | AAAGATTAATGAAAA[C/G]AAGATAATCATTTAC | 79658 |
| rs542046108 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147890719 | ATAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 79658 |
| rs542062505 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147879535 | TTCTGAATTACATGC[A/G]TGGGTTTTAAACCAC | 79658 |
| rs542078346 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147811343 | TAGAACATGTGTGAA[A/C]CCACTGTGTATATTG | 79658 |
| rs542081272 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147890306 | ACTTTGATTATCAAT[G/T]GTTAGATGGATGTGT | 79658 |
| rs542081503 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147890832 | ACTCCATCACAAAAA[A/C]AACAACAAAAAAAAC | 79658 |
| rs542088816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147853196 | CATGCTGGTGAACTG[A/G]CCTAAGAGATGTGGG | 79658 |
| rs542094475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147772274 | ACTTCAGCTCCCTCT[C/T]CCTAGGTTCCGTGTT | 79658 |
| rs542120164 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147827521 | GGAGCTAGAGTTTGT[A/G]GGGTGGAGACACAGC | 79658 |
| rs542137118 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147998457 | ATTGAAACTGGTCTA[C/G]ACCATAGTGAAGGAA | 79658 |
| rs542137478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147778643 | GGGTGTTGCTAATCA[A/G]AATGTCCTATTCCTG | 79658 |
| rs542137889 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147860615 | AATAGTTGTACTGTA[A/G]CAAGTATTGGATATT | 79658 |
| rs542141455 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147904851 | ACAGTCCCACCAACA[A/G]TGTAAAAGTGTTCCT | 79658 |
| rs542142684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147738712 | AAGGCCCTGTTCTTG[C/T]CTCAAAATAGCTGTT | 79658 |
| rs542144017 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148012901 | GAAATGTTCCTTTGT[A/G]GGGGATGGTGGGTAT | 79658 |
| rs542144900 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147953657 | TTTTATTTCCTAATC[A/G]TTCTGGCTGGATTGA | 79658 |
| rs542156424 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147897199 | TTGAGTTCTGTTTTT[A/T]AAAAAATATGCTAGC | 79658 |
| rs542170173 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147964614 | GGGTTATCCTGTTCA[A/T]CCTGTAACATGCAAT | 79658 |
| rs542191706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147940889 | CACAGGAGAAATTGC[C/T]CGTCATCAGTTGGAG | 79658 |
| rs542193419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147764182 | TTGTGAGAAAGCTGG[A/G]TGGGAAAATACAAGG | 79658 |
| rs542196147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148037972 | TTTAACTTTATTTAT[A/G]TAGGTCACCTCTGGA | 79658 |
| rs542196804 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148023176 | TGAATGAACTCCAAA[G/T]CAAATGTTGTGGTGC | 79658 |
| rs542204007 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147815321 | TAAAGTGATTAGTAG[A/C]GTACCTGATGTTATA | 79658 |
| rs542204883 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147873979 | TGCGGGCTTACACTT[C/T]CTTACAGGACATAAG | 79658 |
| rs542209056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147972785 | TTGAGACGGAGTTTC[A/G]TGCTTGTTGCCCAGG | 79658 |
| rs542209394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147799190 | CAGGCATGCATCAGT[A/G]TGCCTGGCTAATTTT | 79658 |
| rs542211829 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147841050 | GACCCATCATTCATA[C/T]GCTGTTTGTGGCTGC | 79658 |
| rs542222448 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147750926 | CTTCAATTTAAAACA[A/G]TGAGCTTTGGAGGGC | 79658 |
| rs542244998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148015975 | ACACTGTGAATGGGG[C/T]TTGGTATGACTGGGT | 79658 |
| rs542257000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147907262 | ATCCAGAGGCACCAA[A/G]ATTCAGTCTGTTGGC | 79658 |
| rs542295536 | snp | A/C | 1.64806e-05 | 0.00287054 | synonymous-codon, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147906710 | GGAAGCTCTGGGTGG[A/C]AAGGAAGCTGTAAGA | 79658 |
| rs542300161 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147851105 | CTATTCAGATGCTAT[C/T]TTGGAAAGAGCCAAT | 79658 |
| rs542332439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911853 | TTTTAAAAGCTTGGA[A/G]CATGGTGTAAAATAT | 79658 |
| rs542347023 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148039238 | ATCAGTATAGTTCTT[C/T]GTGTGGCCATCCTTT | 79658 |
| rs542347931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147733382 | GACCATCCCTTGGAT[C/T]CATAACCCCTTCGGA | 79658 |
| rs542353166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | ARHGAP10 | GRCh38.p7 | 4:147854734 | ATGACATTAAGAACA[A/G]ATGCAGGAAGAAATA | 79658 |
| rs542369181 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147787993 | AACCCAAATAGTTCC[C/T]GGATGTGAGAAAACT | 79658 |
| rs542370434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148000303 | GGTGTATATGTGCCA[C/T]ATTTTCTTAATCCAG | 79658 |
| rs542378754 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147939340 | CCTCACTGGACAGGA[C/G]ATGTAACAACTTTAA | 79658 |
| rs542379844 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147861605 | GAACTTCATTGAGCA[A/G]CAGAACAGTTCTCAG | 79658 |
| rs542383887 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147946120 | AGGCAAGCCTTATGT[G/T]CACAATGACCTGGGT | 79658 |
| rs542399739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147762599 | GCAGTGGCGCAATCT[C/T]GGCTCCTGCAAGCTC | 79658 |
| rs542401107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148045669 | CTTGAACCTGGGAGG[C/T]GGAGCTTGCGGTGAG | 79658 |
| rs542415638 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147791635 | AGTTGCCCAGGCTGG[A/G]GTACAGTGGTGCAAT | 79658 |
| rs542419251 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147906120 | TGCATCTTTTCTTAA[C/T]GCTCCTCTGCCATTT | 79658 |
| rs542419995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148035654 | TACTTGAGCTTGCAG[C/T]GTAACTGAGAATTGG | 79658 |
| rs542427776 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147813123 | TTTTACATGGATTGG[C/T]TTCTGCCTTTAGGAG | 79658 |
| rs542439638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147875418 | ACACTGTGTGCACCC[C/T]AGGAACATGCTTGTA | 79658 |
| rs542452823 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148004948 | TGAGATTATGCTAAT[C/T]TGTTGCACAGCAATA | 79658 |
| rs542455540 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147905640 | GGTTACTGTAGCCTT[A/G]TAGTATAGTTTGAAG | 79658 |
| rs542461203 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147788345 | TCAGCTACTCAGGAG[G/T]CTGGGACAGGAGAAT | 79658 |
| rs542461269 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147758744 | AGCACTTTGGGAGGC[C/T]GAGGCAGGAGGATCA | 79658 |
| rs542484213 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147945961 | GAGGTCTGGCTCCTC[C/T]TTTGCATAAGGCGGG | 79658 |
| rs542487952 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148009400 | GCTTCCCAAAGTGCT[A/G]GGATTATAGCCATGA | 79658 |
| rs542489177 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147735385 | GTTTGTATGTTAGAG[C/T]GGAGGAGGTTTGTGA | 79658 |
| rs542489242 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147812316 | CCTCTTTGAACACAG[C/G]TAGTTTTCAGGAGGT | 79658 |
| rs542520200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911402 | GAGTCTTGCTCTGTC[A/G]CCCAGGCTGCAGTGC | 79658 |
| rs542524769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148009857 | GTTTCCTTTTGGGAC[C/T]TCAAGTGTTGGAAGC | 79658 |
| rs542527550 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148062588 | ACATTAACTTTAAAA[A/G]AAAAGGGAAATATTA | 79658 |
| rs542533345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147826826 | TTCTTAATTTTGTGA[A/G]AAGTTAGGTCATATT | 79658 |
| rs542548646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147926446 | AGAGGAAAGTGAAAA[C/T]GAACTCTAAGCCTCC | 79658 |
| rs542551675 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147778057 | AAGTTGCTTATACTT[C/T]AGGTGGAGGTATCAG | 79658 |
| rs542556274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147910693 | TTTTTTTTTAACTTA[C/T]ATAAAAACGTGATCA | 79658 |
| rs542570929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147753025 | CTATGAGGAGCCTGC[C/T]ACCCAGAAGGTTAAG | 79658 |
| rs542579824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147856469 | ATCCGATATGCTCCA[A/G]AATTTGAAATGACAC | 79658 |
| rs542593719 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147973157 | TGTCAATTTTTTTTT[G/T]TTGTTTTTGTCATAT | 79658 |
| rs542594870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147807515 | GAACGTAAAGAGGTC[A/G]GTGTATTTTAAGTGT | 79658 |
| rs542608215 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147767898 | AACAGGACAGACACA[A/T]TAGAGCCCTTTAGAA | 79658 |
| rs542617116 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148053069 | CTATTTTGTAGATGA[C/T]GTTTCATCTTAATGC | 79658 |
| rs542623207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147742034 | TGTTGACTTGTTTAC[C/T]CACAGGCATCTTCTA | 79658 |
| rs542626932 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147910017 | TGGGCTTTTCTTTTC[-/T]TTTTTTTTGATACAA | 79658 |
| rs542643989 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147844976 | CTTTCCCAGAGCCCA[C/G]AAGGCCCGGCACGCT | 79658 |
| rs542681243 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147876614 | AGGAAAAAAACAAAA[C/G]AAAACAAAAAACCAC | 79658 |
| rs542682904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148000008 | TGTATACATGCGCCA[C/T]GTTGGTGTGCTGCAC | 79658 |
| rs542690041 | in-del | -/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148012295 | ATGGCTGCTATGTCT[-/G]AGAGGCAGTGAGTTC | 79658 |
| rs542702771 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148060747 | CCTAGTAGAGGCTTC[G/T]GAGACACACCCAGGA | 79658 |
| rs542704848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147836948 | CATCTAAAAATAGAA[C/T]TAGTTAGGGCAGAGC | 79658 |
| rs542711322 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147741295 | AAATCCATGAATCTT[A/G]AAGACATTTAACCCA | 79658 |
| rs542715415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147836348 | TTTAATAGGACTAGG[C/T]TTCAAGTTTTTCACA | 79658 |
| rs542728370 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147862506 | CGGGCACCATGGAGT[A/G]CGCAGCCCTGGCTGC | 79658 |
| rs542731795 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148010107 | TCCATTCCCCTCCAC[-/T]TTTTTTTTGTCATGA | 79658 |
| rs542739712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148053683 | ACATTCAGTCTGGGG[A/G]TACAACTTTTGTCCT | 79658 |
| rs542744435 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147773762 | GATTCTTGATTCTCT[A/C/G]CCTTGGTTCTTTAGA | 79658 |
| rs542764344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148060153 | GTGTTCCTTCAAAAT[A/G]TTTTAAATAAAAGAA | 79658 |
| rs542775646 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147927876 | GATACTGGGATCGGG[A/T]GACCTCTGGGAGAGT | 79658 |
| rs542780771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147843421 | TCAGTCATAAATCAA[C/T]TCCAGCCCAGCCCTT | 79658 |
| rs542795899 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147968830 | ATCATATGCCAGACA[C/T]GTAGTAGGTGCCGGA | 79658 |
| rs542822764 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147960308 | TAGCCTTTTTGCATC[C/T]TTTCTGTTTAGCAAC | 79658 |
| rs542827055 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147869065 | ATGAGAACCTTCAGG[A/C]AGGACTGTATATACA | 79658 |
| rs542827904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147874841 | TTTACTGCTATTTTT[C/T]TTTCTTTGCACATGA | 79658 |
| rs542842293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147828577 | TAATCAAGTGATTGA[A/G]AAATTCAGGGAAGGC | 79658 |
| rs542842980 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147794854 | GTGTTCTATCATGTA[A/G]GTATAGGACAGTGTA | 79658 |
| rs542843075 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148024697 | AACTTCCTTTTAGAC[A/G]CTCATTTCAACTTCT | 79658 |
| rs542857396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147974822 | CCTCACAATCATGGC[A/G]GAAGGGGAAAGGCAT | 79658 |
| rs542857912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147960860 | CTGGTTTCTTTTGCT[C/T]ATTTTGTGAGATTCA | 79658 |
| rs542869198 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147880901 | GGTAAGAAATAAATT[G/T]TTACACTAAAAAAAA | 79658 |
| rs542869633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147736933 | GGATGGTTTTCTACT[C/T]TTCTGTATTCTCTCA | 79658 |
| rs542877804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148018325 | ACTAAGAGGAATTTG[C/T]ATCCAGGCAGTAGTT | 79658 |
| rs542878070 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147835689 | TATTTTATTTTCTTG[A/G]TTTAACAGTTTATTG | 79658 |
| rs542890346 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147828511 | AGTAGTGATTCATCC[A/G]TTGGAGGAGATGGCT | 79658 |
| rs542894359 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147746348 | ACCTTGTGATCCGCC[C/T]GCCTTGGCCTCCCAA | 79658 |
| rs542922658 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148011351 | GCTGGGAAATTTTGA[A/G]TAGCTGTGGGCTGGA | 79658 |
| rs542922859 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147894437 | ACTCAATTGTAGGAA[C/T]TATTTAGAAACAAAT | 79658 |
| rs542927288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148064744 | TGACCCATCTCATCT[C/T]GTGGGTCTTCATTCA | 79658 |
| rs542933552 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148058648 | AATGTTTTTAATATG[C/T]GTGGAGCGTAGAGTC | 79658 |
| rs542936497 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147925399 | CTTGCAAAAAGCAAC[A/C/G]GCCCACTTTTGCCTT | 79658 |
| rs542949319 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147841300 | TCTTTTCTTGGCTGG[G/T]TCAAGTATTTTATAG | 79658 |
| rs542951625 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147841941 | ATATTCTTCCTCCCA[C/T]GTCACCCCCAAGATG | 79658 |
| rs542951672 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147811474 | GGCCACATTATCCTG[C/T]AGCCCTGACTGTCCT | 79658 |
| rs542961598 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148072624 | CCTGCCCTTCCTAGA[C/T]GGCCACCTGCAGGAC | 79658 |
| rs542963698 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148027529 | AAAATGAAAATACTA[A/C]TGTTGAGCGGGGCAG | 79658 |
| rs542982632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147966451 | TGCATGGAATTATTA[A/G]GAAAGCCATTGTGGT | 79658 |
| rs542991532 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148008001 | GTTGGGTTAGCATCT[A/T]CCTCCTTCTGGATGT | 79658 |
| rs543001601 | in-del | -/AAAC | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147811600 | TTTTTTAAAAAAAAA[-/AAAC]AAAAAACAAAACACT | 79658 |
| rs543003330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147790160 | TATCTGGTGAGGGCC[C/T]ACTTCCTGACTTGCA | 79658 |
| rs543016712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147976772 | TTTTCCCTTGGGACC[A/G]GAGTGGTTTGATAAG | 79658 |
| rs543022047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147781140 | GAGGCGGGCGGATCA[C/T]GAGGTCAAGAGATCG | 79658 |
| rs543039183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148020171 | ACAACATAGAGCTTA[C/T]TGAGGGTGTGGTGTG | 79658 |
| rs543042213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147756356 | GCTGTTGAATAAACC[A/G]TTTCTGGATCTTCTA | 79658 |
| rs543048327 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889722 | TTTCCTGTGTTGGGA[A/G]GGCAGCTGGGTAGCA | 79658 |
| rs543048428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147883783 | CACTGCAACCTCTGC[C/T]TCCCGGGCTCAAGTG | 79658 |
| rs543051398 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147796441 | GAGACAACAACGGAG[C/G]TTCCTCTTAGAGGAG | 79658 |
| rs543057286 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147970178 | TGAGGAAGAATATTT[C/T]TGCTGACAAGGGTGC | 79658 |
| rs543058179 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147789178 | TCAGTCGTGGAGAAG[A/T]CAATTCAACTGTAAG | 79658 |
| rs543058377 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147752290 | GGGTTGTAATGTCTG[C/T]AAAGCTTACTTTCGG | 79658 |
| rs543067932 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147976424 | GACTGTTCAGTGTAG[A/C]AGTCAAAATCCCATA | 79658 |
| rs543069300 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147876324 | AGGGCTGGGCGCGGT[G/T]GCTCACACTTGTAAT | 79658 |
| rs543078191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148013122 | CTGATACTAATCTGC[C/T]CCCCACCTTCAGGGC | 79658 |
| rs543083049 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147968168 | GGGATGAGATAATCT[A/G]TGGGGGAACATAAGG | 79658 |
| rs543100997 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147882843 | TAGCATTAAGGAAAA[A/T]CCTAGTGTTCATAGA | 79658 |
| rs543105373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147983255 | CAGTGGCACGATCTC[A/G]GCTCACTGCAACCTC | 79658 |
| rs543106287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147748624 | GGCTTGATGGTTTCA[C/T]AGGTGTATGCTTATC | 79658 |
| rs543115665 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147763343 | TTTTTGAGACAGTCT[C/T]GCTCTGTCGCCAGGC | 79658 |
| rs543118357 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147878298 | GACAGGGTTTCACAA[C/T]GTTGGCCAGGATGGT | 79658 |
| rs543120847 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147888809 | TGTGGAGCAAAATCT[A/G]CTGGCAGAAGGTGAA | 79658 |
| rs543122609 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147754484 | AGTGTTCAAAACTAC[C/T]GAGGGCCCCAAACTG | 79658 |
| rs543123737 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148005435 | TTTAAAAAAACATAT[A/G]TAGAAATATATATAC | 79658 |
| rs543125623 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147803088 | ATCTTGGTACACTGC[A/C]ACCTCTGCCTCCTGG | 79658 |
| rs543128917 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147851006 | CTTTTTTGGACATTT[C/G]ACCAAGTAATGAAAA | 79658 |
| rs543145074 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147945057 | ATAGGTTTGCAACTC[A/G]CTTGTGGTGGTATGG | 79658 |
| rs543155654 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148006174 | TGTTAAAAGTTCAGC[C/T]ACCCTGGGCCTGCCA | 79658 |
| rs543164960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147927303 | GCCATTCTAAAGTTA[A/G]ACCTGCCTTTTTTCC | 79658 |
| rs543165763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148067458 | CAGGTCATCTGACCA[C/T]GGCTTCTGTGGAGCC | 79658 |
| rs543166210 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147989737 | TTCATATTGCTCAAA[A/C]ACACATGCTGTACAA | 79658 |
| rs543167785 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148054789 | TAACTTATTCTGAGC[C/T]GTATACCCAGGTAGC | 79658 |
| rs543169320 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147788650 | ATTTGCGGTATTTGG[C/T]GTGTAGAATTTGCAC | 79658 |
| rs543174596 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147974380 | CTCCTCATCTCCCCC[C/G]ACTTCCTAAGGGCCC | 79658 |
| rs543177829 | in-del | -/T | 0.00517822 | 0.0506191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148027896 | TTAGCCATTTGGAAG[-/T]TTTTTTTTGCCTCTA | 79658 |
| rs543201553 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147995411 | AAAATACTGTAATAA[A/C]AATATGTGATCTACT | 79658 |
| rs543221961 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147864687 | AAGTAGCTGCAGACA[A/G]TACATAAATGAATTG | 79658 |
| rs543237050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147888226 | TATGACCTTGTCCAG[C/T]CTTACGACTTTATGT | 79658 |
| rs543238821 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147882267 | GGAGTTCAAGACCAT[A/C]CAGGCCAAAATGGTG | 79658 |
| rs543246594 | in-del | -/A | 0.00524105 | 0.0509221 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147906547 | ACCACAGATAAAAGT[-/A]AAAAAAAAATGGTTA | 79658 |
| rs543260548 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147733343 | ATGGGGCGGAATTAG[C/T]CCCAGTGAGGAGCTG | 79658 |
| rs543262167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147949769 | AGTGCAGGTAAAGGG[A/G]TTGACTGAGATGACT | 79658 |
| rs543268797 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147800884 | TGGCACAATCTTGTC[A/T]CACTGCAACCCACGC | 79658 |
| rs543276662 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147971313 | TGGTGCATTTTTTCC[C/T]CCAGTGCCTGCTGTG | 79658 |
| rs543295552 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147753972 | TCATCTGCTACTACT[C/T]GTTCTAAGAAAGACC | 79658 |
| rs543296170 | in-del | -/A | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147999987 | ACGTGCGGGTTTGTT[-/A]ACATATGTATACATG | 79658 |
| rs543296606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147902696 | CAGTAAGCCGAGACT[A/G]CACCACTGCACTCCA | 79658 |
| rs543303604 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148071646 | AAACAAACAAAAAAA[A/C]ACACAAAAAGCTTGA | 79658 |
| rs543316119 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148065882 | CAGGTGCAGTGGTGC[A/G]CACCTGTTGTGCCAG | 79658 |
| rs543327513 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148001236 | TTGTAGATGTGTGGT[A/G]TTATTTCTGAGGGCT | 79658 |
| rs543330965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147761661 | ACTCTCCATAAAATA[C/T]AATTGCCTGGAATTC | 79658 |
| rs543332767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147988028 | GGCACTTGCAGTTCA[A/G]TAAAGTTACAGATAC | 79658 |
| rs543338041 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147967859 | GCTGCATAGCCATGC[A/G]TATTCTGTTAAATTT | 79658 |
| rs543344986 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147768423 | AATTCTAAAGATTCC[C/G/T]CTGTTAACATCAGCT | 79658 |
| rs543345432 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147760946 | TGTGAAATTAATAGC[C/T]CTCAACTGAGAACTG | 79658 |
| rs543357479 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147859119 | GTATTTGTTTTCCTT[C/T]TGCCTGGTATGTTTT | 79658 |
| rs543358758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147956456 | AAAACTGGTTCTATT[C/T]GTTTTTGTTTTCACA | 79658 |
| rs543366181 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147995922 | TGGGGTTTCACCATG[G/T]CAGCCAGGATGGTCT | 79658 |
| rs543371969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147845313 | TGCGCTTATATATCT[C/T]CTTAGGTGTTCATGT | 79658 |
| rs543373174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147981261 | GGTATATTATGTCTA[C/T]TTTTGTTTGTTTCAA | 79658 |
| rs543382811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147937683 | TCAGTGATAGACTGG[A/G]TAAAGAAAATGTGGG | 79658 |
| rs543387368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147812139 | AATTGACTAACTCTC[A/G]AGGACTTGGATGAAC | 79658 |
| rs543389007 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147804184 | AGTAGCCCCCCAGGT[C/G]TGTTGTTCCCTTCTT | 79658 |
| rs543393020 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148027578 | ACGTGATCATTTCCT[G/T]GTATCCTAAGTAGGA | 79658 |
| rs543410231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147837946 | CAGACAACTTGAACA[C/T]GTATACTTTTAGGTA | 79658 |
| rs543416962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147803540 | TAGAAGTTATTCCTT[C/T]TGTCTAACTCTGTTT | 79658 |
| rs543430101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148028061 | TTCTGTTTGTCACTG[C/T]AGTGAAATAAGAAAC | 79658 |
| rs543442270 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147904693 | GCCACAATAAACATA[C/T]GTGTGCATGTGTCTT | 79658 |
| rs543448444 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147824557 | GTTTAATTGACTCAC[A/G]GTTCCGCATTGCTGG | 79658 |
| rs543450310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147811371 | TTGGGGTTCACTGCT[C/T]CCTAGGGAGTTTGGT | 79658 |
| rs543457562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148019509 | GTAATCCCAGCACTT[C/T]AGGTGGCAGAGGCGG | 79658 |
| rs543459961 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147944757 | AAATAGTCTTTTCCA[A/T]GAACCTCTTACTTTC | 79658 |
| rs543473106 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147753519 | GGCTAATTTTTTGGT[-/T]TTTTTTTTTTTTTTA | 79658 |
| rs543474115 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147896843 | GATTAGGCTATAGAT[C/T]GAAAACGTGATATTT | 79658 |
| rs543479069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147904278 | GGGTACATGTGCACA[A/G]TGTGCAGGTTAGTTA | 79658 |
| rs543482295 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147897915 | TGTTGCCCAGGCAGC[A/G]TGTTCTCAGCTCACT | 79658 |
| rs543483797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147852401 | CAAGTGCTCCATTCT[A/G]TGAGGATGAAGTTGA | 79658 |
| rs543488514 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147855844 | GACATACTGTCCTGG[A/G]TTTCCAGAAGAACAG | 79658 |
| rs543511899 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147796141 | GGAATTATTTAGTAA[A/T]GTGATAGAAAATAAG | 79658 |
| rs543517415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147910170 | GTACCACCATACCTG[A/G]CCAATTGTTTTTATT | 79658 |
| rs543532960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147975883 | CTGTGTTGTTTCACT[C/T]TTGTTAACCCTGCAA | 79658 |
| rs543538171 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147929162 | GTATTATGTTGAATC[G/T]CATCTTTGTACAGCT | 79658 |
| rs543539343 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147997229 | ATACCCAGTGTGGAA[A/T]CTACAAACGTATTGC | 79658 |
| rs543540937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147943794 | AAATTCTGCCTAGTC[C/T]CAGTGCATTCACTGA | 79658 |
| rs543560799 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147785294 | TGTTTTATTTCTTCT[G/T]TTGTGTCTCCAATCC | 79658 |
| rs543565779 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147817877 | GAGAATAGGGGGCAT[A/G]GAGTTACAAATAAAT | 79658 |
| rs543567412 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147769573 | AAGTTCTTTCTACAG[A/G]GATGATTAATACTTA | 79658 |
| rs543577920 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147836978 | CCAAAATGAAAACAC[A/G]TTGGCCTCCTATTTT | 79658 |
| rs543587412 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147774220 | TTCCTATATTTGACC[A/G]TGTTCAGACCAAGTT | 79658 |
| rs543593844 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148022206 | GATAGATGTGCAGAA[C/T]GTGCAGATTTGTTAC | 79658 |
| rs543617170 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148032969 | TGATTAGGTGTTAAT[C/T]TCCTTTGGCAACACC | 79658 |
| rs543629251 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147809804 | AACGTAGATCCCTCA[C/T]GTATGCATAGTTCAC | 79658 |
| rs543646338 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147798835 | CTTTTTACCCCCCCA[C/T]GCTTGAAAAATGTGC | 79658 |
| rs543654382 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147909612 | TTTCTTATTCTATCA[C/T]ATTAACCAGAATCAA | 79658 |
| rs543655849 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148025749 | ACTTAATTTTTTTTA[A/G]AGTAGCTTGAATCAT | 79658 |
| rs543658333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148002521 | ACCTCTGGTAGAATT[C/T]GGCTGTGAATCCATC | 79658 |
| rs543671106 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147902058 | TTACTAGTTACTGAT[A/G]GTATATTGTAGTTGA | 79658 |
| rs543673648 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147950968 | GATTTATATCCCCCA[A/G]CAGATCCCAACGAGT | 79658 |
| rs543677656 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147872204 | TGGAGGCGTCTGCGG[A/C]AGGGATGGTGGAGTG | 79658 |
| rs543680531 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147809355 | TGAAATAGCTAACAT[A/G]CATTTTTTTTCTTGA | 79658 |
| rs543681922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147825384 | CCCGGGAGGCGGAGG[C/T]TGCAGTGAGCTGAGA | 79658 |
| rs543687521 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147995497 | TGTTACCGTATATTA[A/T]GTTTTCCTTATGTAT | 79658 |
| rs543690545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147816805 | ATATGAAGCTAGTCT[A/G]CAATCCTAGAGGAAT | 79658 |
| rs543691018 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147774546 | CTCAGGTTTCTTTAT[C/T]CTATAACATATTTAC | 79658 |
| rs543694564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147816116 | AGTGGGCTAGGTGGT[C/T]GCCAGCATTCTCGTC | 79658 |
| rs543708512 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148007501 | GCTTGATGAGGATAT[C/T]TTCTGGGGATGGGTA | 79658 |
| rs543716658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148001862 | TGTCATCTGCAAACA[A/G]GGACAATTTGACTTC | 79658 |
| rs543722176 | snp | C/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147908848 | GCCCCCTTTATCTTA[C/T]TTTTGCTCATTTGGT | 79658 |
| rs543732850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147790666 | AACCTGAGCTAGAGT[A/G]GCCCACATTTGGTGG | 79658 |
| rs543742256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147915342 | TCGAAAGAATTTCAG[A/G]AAAAATCCCTGCAAT | 79658 |
| rs543745702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147949198 | TGTTATGTGCACTAT[C/T]GTTATTCCTGATTGA | 79658 |
| rs543747104 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147914410 | TCACCCAGGCTGGAG[C/T]GTGGTGGTGGAGCCA | 79658 |
| rs543748080 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147871607 | TAGACAGTGTCCTAC[C/T]GTATAGATTATTGTG | 79658 |
| rs543751194 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147807187 | TGAGGTCTGTTCCCA[A/C]CCCCCAATTCATGAA | 79658 |
| rs543769109 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148050813 | CTTCTTGTCTTTTCC[C/T]CCTTTATCTCTGCAT | 79658 |
| rs543773945 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147742842 | GCTGAATATAGGCCT[C/T]TCATTTATACATAGG | 79658 |
| rs543776292 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148034880 | TTATATTTTTTGTTT[A/T]TATGGGCAAAAATTT | 79658 |
| rs543778158 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147922282 | ATTACTCTGCTGAAG[G/T]GTTGCCTTGCCTTTG | 79658 |
| rs543779649 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARHGAP10 | GRCh38.p7 | 4:147731914 | TGCGCGTGGGGAAGA[G/T]AAGGAAGAGGCGTCC | 79658 |
| rs543784346 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147985778 | TGTGTCCGTCTCAGC[A/G]TCTGTAAGCTTTTCC | 79658 |
| rs543785954 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147959364 | GACTCTATTTTTCTT[C/T]TTTTAAATTTTTTAA | 79658 |
| rs543787672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147953050 | GATCATACAGTTTTC[C/T]TTTCATTTGGTGAAG | 79658 |
| rs543788668 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147982224 | CTGATGGGTTTCTTT[G/T]TATAGGTAACATGAT | 79658 |
| rs543807334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147764779 | GCCTCAAGTGATCCA[C/T]GTGCCTCGGCCTCCC | 79658 |
| rs543811276 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147861114 | CTACTGGCCTGGATC[A/T]CATGCCTGCCAAGGG | 79658 |
| rs543822208 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147960054 | TTGCAGAGTCTCTGC[G/T]TTAAGTCTATTTTTA | 79658 |
| rs543830946 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148012062 | CAAACAATTATTAGC[A/G]TGTCGACAGTAATAC | 79658 |
| rs543847560 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147952102 | GTTCATTCCATCTCA[C/G]TGCTAACTAATGGAC | 79658 |
| rs543848848 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147860741 | AGATTTCCTAAATAA[C/G]TTTATGTGAGACTTG | 79658 |
| rs543850834 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147818625 | CTCCCTGCCCTGCAT[C/T]TAACCCAGGCAGAGA | 79658 |
| rs543870283 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148068050 | ACGTTCCTGTGATGG[C/T]CAGAGGGACCTTTCC | 79658 |
| rs543892443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148057873 | GCCTGACAGGAAGTC[C/T]TCAGACTGTAAATGA | 79658 |
| rs543899951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147738777 | TTTATTACCCCTAAC[A/G]GTATATTTCTCCAAA | 79658 |
| rs543907486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147840879 | GCAAATATTGTAAAT[A/G]TATATTTTTTAAAAA | 79658 |
| rs543919937 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | ARHGAP10 | GRCh38.p7 | 4:147730259 | CGTGGACTTGCTGGG[C/T]CACACGGTAACCTCC | 79658 |
| rs543921005 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147998035 | TGAGAGAAGTTTATA[G/T]CCTTAAGTAACTGTA | 79658 |
| rs543923075 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147734651 | GGTTAGGGCGTGGCT[A/G]TAGGAAAATTGAGCA | 79658 |
| rs543934867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147777359 | CACCTCCCGGGTTCA[C/T]GCCATTCTCCTGACT | 79658 |
| rs543934871 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148042430 | CTGCATTTGACCCTG[A/T]TCTCCAACAAAATCC | 79658 |
| rs543949777 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147930195 | AATTTGAGAATGTAT[C/T]TCTGTAGAATCATAC | 79658 |
| rs543963171 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147990667 | TCTATTAAGTGAACT[A/C]ACATAGGAACAGAAA | 79658 |
| rs543966630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147840287 | AAACCTGGCTTTGCT[C/T]CCTTTAAGCAAATCA | 79658 |
| rs543970029 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147745703 | TCACCGTGTTAGCCA[C/G]GATGGTCTCCATCTC | 79658 |
| rs543973726 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147739710 | AATTCTGTGACTTCA[A/G]TAGCTGTTTGTCACC | 79658 |
| rs543976995 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148057036 | CTCAGCCAAGTTTCA[C/G]TTGTGGATGACACTA | 79658 |
| rs543983788 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147872670 | CTATGTATGATATAC[G/T]GTGTTCTTACAATGA | 79658 |
| rs543995712 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147933933 | GAGCTGAGCCTGGGT[C/T]CCCTTAGGATCTGTT | 79658 |
| rs544001707 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147792793 | TTCACTCTGTGAACT[C/T]CTTTTCAGCTGAGCT | 79658 |
| rs544014614 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147957908 | TTAAAGGTTGACTGC[A/G]TTGGAAAAGTTAAAA | 79658 |
| rs544018112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147865780 | TATGGTTTAGTTGGA[A/G]CGATAGTCATTAACC | 79658 |
| rs544030683 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147968788 | ACTCATTTGTTTATT[A/G]AAAAGATTTTTTTAA | 79658 |
| rs544037773 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147915792 | AGTTTAAAAGAATCA[A/G]CAGAACTTATTATTG | 79658 |
| rs544047027 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147971465 | GAATGAGCGAGAAAG[C/T]GGCGGAGACTTCAGA | 79658 |
| rs544057468 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148021884 | TTTGTCTACAGTAAC[A/T]TAAATCATTTTTTAA | 79658 |
| rs544058764 | snp | A/C | 0.302686 | 0.244385 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147832646 | AGCAAGACTCTGTCT[A/C]AAAAAAAAAAAAAAA | 79658 |
| rs544080059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147875576 | ACGTATACGTCCTCT[C/T]CCTCCCATAACCCTG | 79658 |
| rs544090360 | in-del | -/C | 0.123105 | 0.215401 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148029994 | CGTGAGGCTCAGCAT[-/C]CCCCCCCCCCACCAA | 79658 |
| rs544100137 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147931355 | AAACACATTGACCAG[C/G]TTACAAATTTTTGTT | 79658 |
| rs544103138 | in-del | -/A | 0.309599 | 0.242792 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147910350 | GTGAGTCTTTCTCAA[-/A]AAAAAAAAAAATTGT | 79658 |
| rs544103808 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148008279 | TGCTCAGGAAATTAA[C/T]CAGTATCTCCCCCAG | 79658 |
| rs544110147 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147750336 | TCTTTCTGACTGTGG[C/T]GTCAGTTTAATGAAT | 79658 |
| rs544116816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148055462 | GGGAGACTGAGGCAG[A/G]CAGATCACTTGAGGT | 79658 |
| rs544120539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148048270 | GTGGCTTTTTATAGT[C/T]ACTGCTGGATTCACA | 79658 |
| rs544136609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147970609 | AGGAAAGTCACTAAA[A/G]CAAAGAGGAAACTTC | 79658 |
| rs544152939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147797677 | CAGCCTCCCAGAGTG[C/T]TGGGATTACAAGCAT | 79658 |
| rs544155465 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148055915 | GGGGATTCTCCATCC[A/G]AATTGTCTTCATCTC | 79658 |
| rs544160217 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147898743 | GTAGGAAGTTTCAAA[C/T]CTTCCCACATCTTCC | 79658 |
| rs544170085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147963724 | TCTGAAATCAAGACG[C/T]TGGGAGGGCCGTGCT | 79658 |
| rs544170838 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147766958 | GATTCAAGCGATTCT[A/C]CTGCCTCAGCCTCCA | 79658 |
| rs544172502 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147973301 | CCTGTTAGCTTATGT[C/G]TGAGGTAGGGAGTTC | 79658 |
| rs544180221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147778707 | TGATTCCTGGATGTC[A/G]CTCCTTTTTGCTCCA | 79658 |
| rs544180555 | snp | C/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147881632 | GAAAGAGCGAGGCTC[C/T]CTTCTCAAAAGAATC | 79658 |
| rs544200932 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147787383 | TGAACACAACATCAG[C/T]AGGGGGAGAAGATGA | 79658 |
| rs544216965 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147881016 | CACTGGCTCACGCCT[A/G]TAATCCCAGCACTTT | 79658 |
| rs544218115 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147874071 | GTTTTCCCTTTTACA[A/G]TCTACATTTATCAGA | 79658 |
| rs544220108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147827619 | TTAAGCAGCTAAAAT[A/G]GTTGCCAGTACATTC | 79658 |
| rs544222977 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147923512 | TAAAAAATCTTCCAT[A/C]TGTGGATAATTTGAA | 79658 |
| rs544240542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147786491 | TTTTCCGCTTTTTCA[C/T]TGATCTCTTTCCCTT | 79658 |
| rs544242123 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147870312 | GTGATCTGCCTGCCT[C/T]GGCCTCCCAAAGTGT | 79658 |
| rs544259757 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147860104 | ATACTGAACAAAGGC[-/T]TAGAAACGTACATAA | 79658 |
| rs544261364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148008658 | TCTGTTGGGTTGGAT[A/G]TTTTTAATCTTGTTA | 79658 |
| rs544272392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148004227 | CTTTGAAGGGCATCT[C/T]TCTGCTATCAAATAC | 79658 |
| rs544272415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147999054 | ATGGAAGAACTGTTA[C/T]GCTAACATTGAGAGA | 79658 |
| rs544291771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148059823 | TATTAATCACAGCAA[C/T]GACAGTATCAGTGTT | 79658 |
| rs544293075 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147753220 | TGGAAGGAATGTCCA[A/G]CCTTCTTACACCATA | 79658 |
| rs544295079 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147979700 | TTATTTGTATTGTCT[A/G]TGATATCTTTCAGCA | 79658 |
| rs544295846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147887059 | ACCCTGCCCGGCCCA[C/T]GCTATGTTTCCTTAG | 79658 |
| rs544302657 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147901364 | CTGATCCCTTTAATG[A/T]TAAAGTAATGCGTTG | 79658 |
| rs544328438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147745430 | GACCCAGATTACGTG[A/G]TCAGTGGGAGAGGAG | 79658 |
| rs544331799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147972897 | GTAGCTGGGATTACA[A/G]GCATGTGCCACCATG | 79658 |
| rs544335173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148016098 | ATGTCAGGCATGTGG[C/T]AAGTACCCAAAAGTT | 79658 |
| rs544336644 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147965576 | TGGAGAAATTAGCCC[G/T]TTCTTTAAGTATAGA | 79658 |
| rs544350469 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147855431 | TATGTAATATCAATA[C/T]ATTGGACTTAGTTGT | 79658 |
| rs544357030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147849540 | GGGATTTAAGAAAAA[A/G]GTCTCTAAAAGTTGA | 79658 |
| rs544370176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148063881 | GGTGAGAAGCTGGGC[C/T]TGGTGTGCCTTTCTT | 79658 |
| rs544375023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147807725 | ATACCAGAGACATAA[C/T]TGTAATCAAATAAGA | 79658 |
| rs544392209 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148003738 | GGATTGTAACCCTTG[A/C]CTTTTTTTGTTTTCC | 79658 |
| rs544393171 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148071731 | CTGTGCATGTTCGTG[C/T]ACAGTGGATTGGAAG | 79658 |
| rs544401216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147972049 | GGAAGGAACAAAGGG[A/G]TTTGGGGGAGGAGTA | 79658 |
| rs544410325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147940618 | CTGTGTATCAAACCA[A/G]TCTGTCATTATGATC | 79658 |
| rs544413226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147862137 | TCCCTCCTGTGCTTG[C/T]TGGCATCCAAAGTCC | 79658 |
| rs544415239 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147854879 | TTGTTTCTTGGCTAA[A/T]TTCTTTCTTCATAAA | 79658 |
| rs544423629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147751705 | TTGTGTTTCAGAGAC[C/T]GTGCCCAGTGTTTTC | 79658 |
| rs544434382 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147885716 | ACCATTCTGGTTCTC[C/G]CTCAGATCTCTTGGT | 79658 |
| rs544509505 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148043498 | AAATCTTTATTCCCA[C/G]CCAGGGGTGGTGGCT | 79658 |
| rs544509889 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147757866 | GATCTGGTGCCCATC[C/T]CTGTCCAGTCACCTG | 79658 |
| rs544521988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147757371 | GCTAATTTCTTTTGT[A/G]TTTTAGTGGAGATGG | 79658 |
| rs544523900 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147765542 | TGGTGGCTCATGCCT[C/G]TAATCACAGCACTTT | 79658 |
| rs544532889 | in-del | -/T | 0.0162398 | 0.0886349 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147751666 | CCACTGCACCTGGCC[-/T]TTTTTTTGCTTTTTT | 79658 |
| rs544535683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147853953 | ACCAATGGTTGAATC[A/G]TCTCTTCCTTTTTTT | 79658 |
| rs544545589 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147899248 | AAAATTCCACTGTTT[C/T]CTTTGTCTGTGATGG | 79658 |
| rs544549229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147953740 | TTATTTTTCTGTTTT[C/T]GATTTAATTGATTTC | 79658 |
| rs544556645 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147797580 | ACCACACCCAGCTAA[A/C]TTTTGTATTTTTAGT | 79658 |
| rs544557857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147773644 | TTAAAAACAGTTATC[C/T]GTTTTTCGTGGGCAG | 79658 |
| rs544579306 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147926522 | AGCAGTAGGTTTGGG[A/C]GGGATAGAGACTGGT | 79658 |
| rs544580108 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147876359 | GCACTCTGGGAGGCC[A/G]AGGTGGGCAGATCAC | 79658 |
| rs544581563 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147835159 | TCACACCTGAGGATA[C/T]AATGAGGAAACCCTT | 79658 |
| rs544581866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147809206 | ATAGCAAGACCTCGT[C/T]TCTATAAAAAACAAA | 79658 |
| rs544584974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148016731 | ATTGAGGGCTTAGTC[C/T]CCAAGACTGCCCCCT | 79658 |
| rs544588201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147801700 | TAATGAAGGTTGGTG[A/G]CACCACCCAAGCGAA | 79658 |
| rs544594189 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148000335 | CTATCATTGATGGAC[A/T]TTGGGGTTGGTTCCA | 79658 |
| rs544609046 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147981047 | CTTTAGTATGGTATT[C/T]TTGGGTCTTGGTTTC | 79658 |
| rs544620838 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148024767 | TCATTCTTTCTCAGC[A/G]GAGTTGTTAATAAGG | 79658 |
| rs544623265 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147946205 | TATCAATACACAGTA[G/T]GAGGGCAACAATGCC | 79658 |
| rs544623605 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148009918 | GCTGCTTTTGTGAAA[C/T]CTCAGTTTCTGGTAT | 79658 |
| rs544627524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147868877 | CGCTCACCTCCTGCC[A/G]TGTGACCCGGTTCCT | 79658 |
| rs544630260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148051830 | TCCCATATACAGCCT[C/T]GTGCATGTCATCATA | 79658 |
| rs544632722 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147838190 | TTCCAGAGCATTGAT[A/G]GCCACATCTGCCTGA | 79658 |
| rs544645338 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147808419 | AGTGAGCAGAGGTCA[C/G]ATCATGCAGGGTCTT | 79658 |
| rs544666564 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147800087 | TTGGTGGTTAGATGC[C/T]GCTAGGGCTGCCGTC | 79658 |
| rs544670376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147895193 | TAAATTTTCCTAAAT[A/G]TTTTATGTTTCTGCA | 79658 |
| rs544670850 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147841969 | ATGGAGTCTTGCTCT[G/T]TCACCCATGCTAGAG | 79658 |
| rs544716200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147925509 | AAATTTATTTAGCTG[C/T]CCCATCCTTTCCAGC | 79658 |
| rs544730019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147848741 | TTACTTTTACTTGCC[A/G]TCTATTCTACTGGAA | 79658 |
| rs544750192 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147775171 | ACTCGCCTCGGCCCC[C/G]CAAAGTGCTGGGATT | 79658 |
| rs544750964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147933301 | AGGTGCAGTCATAGC[A/G]CACTATGGCCTTGAA | 79658 |
| rs544757101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147931513 | TATCTATAGTTCTAT[A/G]TCAAATTCAAGTCAG | 79658 |
| rs544764776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147780978 | GCTCCAGAGAATGAG[A/G]GAAGACGCAAGGGCT | 79658 |
| rs544780460 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147816904 | CTTAGAGTCTGTACC[C/T]TGTTCCTCTTTAGAT | 79658 |
| rs544799482 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147995369 | TTAGAAACCCTGGCT[C/G]TAGGTGAAAACAGCA | 79658 |
| rs544816470 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148038676 | GATTATTGGTTTTGA[G/T]TGGGTGGCCCTATTT | 79658 |
| rs544824043 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148048825 | GCTTGATATTTTTGG[G/T]CATAAATCAAATGAG | 79658 |
| rs544836250 | snp | C/G | 0.000117717 | 0.00767104 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148023202 | GGTGCTGGTTTACTG[C/G]AGTAACACACAGGTT | 79658 |
| rs544840916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147870535 | TCCCCATCTGATAAT[A/G]CCTATTGTATTGTAA | 79658 |
| rs544848714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147899550 | CCAGGTGGAAGCAAC[A/G]GTTCTCTAATGATTA | 79658 |
| rs544849503 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148000324 | CTTAATCCAGTCTAT[C/G]ATTGATGGACATTGG | 79658 |
| rs544857522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147961655 | CAGGTGTTCTGAAAT[C/T]CCACTCTTCTCCCCT | 79658 |
| rs544860655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147813748 | AAAGCAAGTTGCTCA[C/T]ATGTTTTCCTGGTCT | 79658 |
| rs544860753 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147805892 | ACGCCTATGAAACTT[C/T]ATGCTAACACAAAGG | 79658 |
| rs544861041 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147942039 | TTAGGGGCATTTTTT[C/T]CTCCAACTTTTCCCA | 79658 |
| rs544868768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147766353 | CATATGCTTTAAATC[A/G]TCTCTACATTACTTA | 79658 |
| rs544885159 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148045628 | CTGTAATCCCAACTA[C/T]TCGGGAGGCTGAGGC | 79658 |
| rs544910593 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148005659 | TGCTGGAGGGACCAG[G/T]TTTTAATTTGAAGAA | 79658 |
| rs544913632 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147782479 | CAGCAGAAAGAGTCG[C/T]CTTAACATCAGCAAG | 79658 |
| rs544923201 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147820062 | AGGGCCACGGTGCCT[A/G]GGACTAGCCCTATCC | 79658 |
| rs544925032 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147789383 | CTACCTCTGCCTCCC[C/T]GGTTCAAGCGATTCT | 79658 |
| rs544925163 | snp | A/G | 0.140919 | 0.224948 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147905676 | TAGCGTGATGCCTCC[A/G]GCTTTGTTCTTTTGG | 79658 |
| rs544928352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148036300 | GCTTCATGAAGAAAA[C/T]TATCTCACTCAGTTC | 79658 |
| rs544929245 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147908348 | GAAAAAAAATAATGG[C/T]ACTTTGGAAAGTCAG | 79658 |
| rs544936918 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147788031 | AATTTACTTTAGGAT[G/T]TATCATCGGTTCCTC | 79658 |
| rs544940319 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148010521 | AATGTTTACAATAAA[C/G]ATTGTATACCCTTTA | 79658 |
| rs544954974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147934792 | AGAGCTGTTATCACA[C/T]CACTGCATTCCACCT | 79658 |
| rs544956763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147769009 | TCCCAAAGTGCTGGG[A/G]TTACAGGTGTGAGCC | 79658 |
| rs544980161 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147949929 | CTTTTTATTTAGTAC[A/C]TAGGATTTCTTTTTG | 79658 |
| rs544984313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147981431 | AGAAGATGCTTGGTA[C/T]GATTTCAGTTTTTAA | 79658 |
| rs544986324 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148072754 | TCAAGGTCTCTGTAA[A/G]TGAAATAAACTGTAA | 79658 |
| rs544993550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147941704 | TTGTTTTGAGTAATC[C/T]ATAAATAATTCCTAG | 79658 |
| rs544994918 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147850416 | TTGGGTCCACACTAC[C/G]TTTATGAGCTGTAAC | 79658 |
| rs544999971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147863901 | TGACATCCTCACCAA[C/T]ACCACTACTTTTCTT | 79658 |
| rs545013206 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148026800 | TATGAAAAAGCAAAA[C/T]ATGACGTAGGCTGCT | 79658 |
| rs545018707 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147956641 | GGACAATTGTTTCAT[G/T]TTGTTTGCCTTAGAG | 79658 |
| rs545019262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147967828 | ATCAGAATCACCTGA[A/G]GGCCTCTTGTAAGTG | 79658 |
| rs545023698 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147866480 | TGCAGAACATGCCAT[A/G]TAAGCTGTCTAATGG | 79658 |
| rs545027810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147815990 | TTTGTTACTACAGCA[A/G]TAAGAAATGAATACG | 79658 |
| rs545030328 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147824385 | ACTATCTAGAATTAC[A/G]TTATAGTGTAAGTGT | 79658 |
| rs545039207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147864733 | AATACTTTATTTACA[A/G]AATCAGGCAGCACAC | 79658 |
| rs545044638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147861525 | TTCCTTGGGTCCCAA[A/G]TTCTTGTCCCACATC | 79658 |
| rs545050977 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147800809 | CCTTGTCATTCATTA[-/T]TTTTTTCCTTTTTCT | 79658 |
| rs545055352 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147777158 | TTTGCGTTTCAGCTA[C/T]GTATCTCTGGCCTTT | 79658 |
| rs545095304 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147735526 | TTTCAGGGAGTAGTA[G/T]ACTGGGATGGATGGA | 79658 |
| rs545101574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147830548 | TTTGATGGGGGGAGC[C/T]TTGCTTTGTCTCCCA | 79658 |
| rs545104224 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147807436 | GAACTTATATTCCAG[A/G]ATTATTTTTTTTTTA | 79658 |
| rs545107375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147988230 | GCCATTCAAACCTGA[A/G]CCTATTGGTTGACTC | 79658 |
| rs545112385 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147857163 | TTATTCCATTTTAAA[C/T]GAATTCCACGTCTGT | 79658 |
| rs545119995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147921184 | TGAAGTTGTACCAGT[C/T]ACATTTAGCAGTTGG | 79658 |
| rs545121097 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147908933 | TTTGCATCTGAGCAT[A/G]TGATAGTGTGTTATT | 79658 |
| rs545128861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148071850 | GAGCCTGTCAATGAC[C/T]CTGGTGCAGACTTTG | 79658 |
| rs545135635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147767938 | AGATATGAGATTATC[A/G]AATTATGAAATGTGT | 79658 |
| rs545141508 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148006621 | TTGTGAATTTGATTT[C/G]CCTGTTGACTTACTT | 79658 |
| rs545142165 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147899704 | GTAAAATTAGGCAAC[A/G]TGCTTTTATCATCTC | 79658 |
| rs545153340 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147999598 | CTAAGTGCCCATGTT[C/T]GTCGTAATGGAGCTG | 79658 |
| rs545158603 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147928769 | TAAAGGCCTTGGTTA[A/G]GACATTTATATGTAT | 79658 |
| rs545159720 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147914426 | GTGGTGGTGGAGCCA[G/T]AGCTCACTGCAGCCT | 79658 |
| rs545167227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147948391 | CAATTTTTACCAACT[A/G]TCTTCAAAAAGTCTT | 79658 |
| rs545170919 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148053777 | GCCCCTTACATGCTT[C/T]GATACACATCCATTG | 79658 |
| rs545187316 | in-del | -/T | 0.320096 | 0.239972 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147761018 | TAAGTTAGAGTTAAC[-/T]TTTTTTTTTTTTTTT | 79658 |
| rs545187664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147862833 | ATCACCCTTCTTATG[C/T]CTTTATTAAATAGTC | 79658 |
| rs545188470 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147747688 | AAAAATTAATCTGAA[C/T]TTTTTCTTCCCCTTT | 79658 |
| rs545191016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147870105 | AGGCTGGAGTGCAGC[A/G]GCCCAATCAATCTCG | 79658 |
| rs545193949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147734258 | TTTCTGTGACAGCAT[A/G]TTAGCTTTCCTGCCA | 79658 |
| rs545197043 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147741124 | TGACATTTAAAAGGA[C/G]TTTGTTAATTGATGT | 79658 |
| rs545197224 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147976978 | AGAAAGAAGAACTTC[A/G]TAATATTTATAATAA | 79658 |
| rs545204482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147955067 | ACTTTCCGTGATTAG[A/G]TATGAAATACTGTAT | 79658 |
| rs545207773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148054388 | TCTGGGCCGGGGTGA[A/G]GTTTCCAGATACCAC | 79658 |
| rs545211200 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148038103 | TCAGTGTAGCATTAG[A/G]TACTACTTTTTGACA | 79658 |
| rs545212470 | in-del | -/AAAAC | 0.0349483 | 0.127486 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147860440 | CTCCGTCTCAAAAAC[-/AAAAC]AAAACAAAACAAAAC | 79658 |
| rs545212922 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147901825 | TGTATTTGCTGCTCT[A/G]TGTGTAACTGGTGAA | 79658 |
| rs545217137 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147963007 | CCACATAACTTTTTC[C/G]TCCTAATTAGTTCTT | 79658 |
| rs545219538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147821419 | TTGGTGCTTTTCTTC[C/T]ATACTTTAGGTGTAA | 79658 |
| rs545223302 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148061387 | ACTGTGGCCTTAATT[G/T]CCTGCCAGGGCTTCA | 79658 |
| rs545229690 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147785145 | AGCTCTGAATATTGA[A/C]TTGTTTAGCTTTCAT | 79658 |
| rs545235570 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147837027 | CGTAGCGAAATCGAT[G/T]GTGAAACTTTTTCAC | 79658 |
| rs545249266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147829767 | TGCTGTAGTGTTTAT[A/G]TTGTTCTTTTAAAAG | 79658 |
| rs545261203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147802304 | CATAGGTGATCCATA[A/G]GCTAAAATGAGATGT | 79658 |
| rs545265783 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148058816 | CCACTGCTGCACGTG[A/C]AAGCTACAAGGTCTT | 79658 |
| rs545270169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147789244 | ATATTTCATCAAGGT[A/G]CATTTCTATTTAAGT | 79658 |
| rs545302843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148012242 | GCCTAAGTGAAGTGA[C/T]ACCCATTGAGAGAAC | 79658 |
| rs545307317 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147757465 | CCTTCCAAAGTGCTC[A/G]GATTACAGGTGTGAG | 79658 |
| rs545314999 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147829327 | CATCGTGCTGGGATT[A/C]CAGGTGTGAGCCACC | 79658 |
| rs545318268 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147739897 | CCTGCCACCACACCC[C/G]GCTAATTTTTGTATT | 79658 |
| rs545323299 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147835779 | GAAACTAAAATTTTC[A/T]CTTATGTAAAACAAA | 79658 |
| rs545327475 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148028831 | ATGTTAAAGCAAATC[A/G]GGGACTTCTCAACTG | 79658 |
| rs545330639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147961140 | TGCCAAACAGTTCTT[C/T]AGAGTGGTTGAACCC | 79658 |
| rs545332179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147888412 | TTTGAAAGTTTTCCA[A/G]TAAGTCTTGGGAGTG | 79658 |
| rs545334398 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147948106 | CCACCATGTCCGGCT[A/T]ATTTTTTGGTATTTT | 79658 |
| rs545351065 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147872023 | GGGAGGATCATTTGA[G/T]CCTGGGAGGTCGAGG | 79658 |
| rs545352626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147843935 | CATTTCCATTTTTCT[A/G]CCGTCCTACCTCTCT | 79658 |
| rs545367581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147970708 | CTTTGGAGATGACAA[C/T]TTTTCCTAGCCTCCT | 79658 |
| rs545370094 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148045119 | TTCCTTGGAGTTTCA[A/G]TGGTACAGTTGGTTA | 79658 |
| rs545375571 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147863490 | GCTACATTTTATTTA[C/T]TCATCCATCCATCCA | 79658 |
| rs545375715 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147878391 | TGAGCCACTGCGCCT[A/G]GCCCATACTTCATTT | 79658 |
| rs545376792 | in-del | -/GAAAGTA | 0.00874735 | 0.0655527 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147907524 | AAAAGAGAATGGTTT[-/GAAAGTA]GAGGAGGGATCATGT | 79658 |
| rs545395789 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148058564 | TGGTGCAACTGGTGT[C/T]GAGTTTTAACAGTTA | 79658 |
| rs545405123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148033103 | TTATTCTCTTCTTCA[C/T]TGAAGAGTCAGTTTG | 79658 |
| rs545410436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147935349 | GAAAATAAAAAGATA[A/G]AAGACAGTGTTCAGA | 79658 |
| rs545413903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147935215 | GATGAGGTGAGGCCC[A/G]TCATGGATGTGTGCG | 79658 |
| rs545426239 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147751049 | CCGGGTGTGATGGTG[C/T]GTGCCTATAGTCCCA | 79658 |
| rs545431737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147915152 | AGTGTGTAGGATATC[A/G]GCGGAGTAGGAGCTG | 79658 |
| rs545432531 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147967174 | CAAATTCTGTGTGGC[A/T]CAGCAACCCTGTACT | 79658 |
| rs545448652 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148050681 | CCCGGTTGATTCATC[G/T]TCTTTCTTATAAAGA | 79658 |
| rs545453509 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148055943 | CTCCCCCAAACCCCA[C/T]GTCCCTTCCAGGCTT | 79658 |
| rs545457792 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148062661 | TCGAAGTCTTTGGCC[C/G]TCTCTAGAGGAAGCC | 79658 |
| rs545464522 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148001632 | AGAGGTCCTTCACAT[A/C]CCTTGTAAGTTGGAT | 79658 |
| rs545464564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147995953 | CCATCTCCTGACCTC[A/G]TGATCCGCCTGCCTC | 79658 |
| rs545487232 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147837748 | TACCTTACTGCAAGC[A/C]AGTGTCTGTCATTTT | 79658 |
| rs545488478 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147750424 | AATTCAGCTTTGTGT[G/T]TGTGCATTGTGTTTG | 79658 |
| rs545494309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147976910 | TGTTGTCTGAGAAAG[C/T]ATACTGAGTACAAGT | 79658 |
| rs545498329 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147744276 | TATTCTCCAAGTGCA[A/G]GGAAAATGCATCTGA | 79658 |
| rs545499661 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147778820 | GTGAGTGGTACAGGG[A/C]ATGAATTCTGTTGGA | 79658 |
| rs545505082 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147941075 | TGGAAGAATTTAATG[A/G]GAGTACAGCATCTGC | 79658 |
| rs545507801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147913971 | CATCCTGGCGAACAT[A/G]GTGAAACCCCATCTC | 79658 |
| rs545519836 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147789978 | ATGAACAGAAAGGTG[G/T]GTTGGTGTGTGGATT | 79658 |
| rs545524703 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148007561 | CAGCTATTCAAGCCC[G/T]TCATGCGGTGTGTGA | 79658 |
| rs545529160 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147970228 | ATGGATGCGTGGATC[A/T]ATGTTAGCCACGGGT | 79658 |
| rs545550377 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147749433 | TTTTGAAGAAACAAA[A/G]CATTGTTAAGAAAAA | 79658 |
| rs545554421 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147781686 | CTTTTCTTTTCTTTT[C/T]TTTTTTTTTTTGAGA | 79658 |
| rs545554808 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147968886 | GTGGGAAAGCAGGTC[A/G]TCATCTGGGGGCGGA | 79658 |
| rs545558191 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147877115 | GGAAAGACCTTGATA[C/T]TTGGGGCCAGAGATT | 79658 |
| rs545559901 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148067609 | TGTTCACTTATCCAT[C/T]TGGAGTCTTCCAGCC | 79658 |
| rs545566679 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147937863 | ATATGCCTGTAATCC[C/T]AGCTACTTGGGAGGC | 79658 |
| rs545567881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147852540 | GTTAAGGGAGGGTGT[A/G]CCTTCTCCCTGCTGG | 79658 |
| rs545575925 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147881614 | CTGCACTCCAGCCTG[A/G]GTGAAAGAGCGAGGC | 79658 |
| rs545581458 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147796277 | TATAATTAATCCTTG[A/C]CCTTGGGGAATATAT | 79658 |
| rs545588560 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148015705 | CGAAGTTCAGGTTGC[C/T]TGGGAGTGAACCTAG | 79658 |
| rs545592206 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147845421 | TCCCCATCACCTGGC[A/T]TTGCATGCTTAACAG | 79658 |
| rs545599060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147883548 | GCTCTCTCAGGTAGT[C/T]GTTACTGTTTCCATT | 79658 |
| rs545601934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147888892 | GTGTGAATGAGATAG[A/G]CTCTTCTCTTGTCTA | 79658 |
| rs545615863 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148006225 | TCACCGTGTAGAGAG[G/T]CTACAGAGACGGGGA | 79658 |
| rs545620772 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148062647 | GCTGTTCATTGGTTT[C/T]GAAGTCTTTGGCCCT | 79658 |
| rs545635962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147882940 | TTTTAGGTAAGGCTG[C/T]TCTATGTTTGTATAA | 79658 |
| rs545636215 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147748782 | TTGAGACCAGCCTGG[G/T]CAACATAGACCCTAT | 79658 |
| rs545641208 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147983879 | AGTCTGGCTTTTTCT[A/C]CTGCTGGAGTTCTTA | 79658 |
| rs545647180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147936839 | GACTTAAATCAGGGG[C/T]CCCCAATCCCCAGAC | 79658 |
| rs545653885 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147786805 | GGTGGGTTACAGAAA[C/T]GAGTCTGTATTCAGC | 79658 |
| rs545661161 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148066512 | CAGGTCTAAAGTCCC[G/T]AGATGATTTGGAGTC | 79658 |
| rs545678402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147851637 | AGAGCAGAAACAATA[C/T]TGATTTAGTTTAATT | 79658 |
| rs545683932 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147943968 | TTTCCATAGACAGAA[C/T]ATGATTCTCAAAATA | 79658 |
| rs545710931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147825161 | GGATTTAAAAAGTGA[C/T]AGAGGGCTGGGCGCA | 79658 |
| rs545714538 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147858461 | TGTGTAAACCTGGAT[C/T]ATATTTAAATGTTAG | 79658 |
| rs545718497 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148060907 | ATGTGGAGAACTTGA[A/C]CCTGGACAAGGACTG | 79658 |
| rs545722041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147754538 | AGTGGGGGTTGTTAG[A/G]AATTTAGTTCCTTTG | 79658 |
| rs545723449 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148018969 | TTATGAGAAAGCTTG[C/T]TACCTAGTAGGTGTT | 79658 |
| rs545735596 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147950495 | TAGCTTTTCTCACCC[A/T]AAAAAGCTCTTGCCC | 79658 |
| rs545744752 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147880105 | AGAGTTGGCTGTGTA[C/G]GAAAGGTGATCTTTA | 79658 |
| rs545748571 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147974898 | CTTTATAAAACCATC[A/G]GATCTCATGAGACTT | 79658 |
| rs545762269 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147853311 | TCGGTTTTTATTTTT[A/C]CCTTATTAATGTTAT | 79658 |
| rs545772565 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147805656 | CAAAATAATAATTTA[A/T]AATTTAAATTAGGCC | 79658 |
| rs545782795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147891674 | AATGAATACCTACCA[C/T]AGCTAAAAGAAGGGT | 79658 |
| rs545787007 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148021934 | GGGGGCAGTATGGGA[C/G]TATAAAGCAAATGCT | 79658 |
| rs545796207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147885061 | GGGGATAAACTGGAT[A/G]TTGCAGTAGAGGGTG | 79658 |
| rs545818190 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147899135 | CGCTTGAGGTCCCAC[A/G]GACAAGAGTTGGAGG | 79658 |
| rs545824257 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148022434 | AATGTATTTTACTTT[A/T]TGACTTTATTGAAGA | 79658 |
| rs545826189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147851388 | TGGCTAATTTTAAAA[C/T]TATTTTTGTAGAGAC | 79658 |
| rs545834767 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147890208 | TTCAGAGGTCCATGA[A/G]TTGTTTTAGTACTTT | 79658 |
| rs545856776 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147898723 | TCCATCTTCAAAACC[A/T]TTCAGTAGGAAGTTT | 79658 |
| rs545875055 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147998862 | AGTATTCTGTTTAAT[G/T]GTTGAAATGTTTATA | 79658 |
| rs545881877 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147845816 | CATGCACTGTGAAAA[A/C/T]GTATGCTAGCACTTC | 79658 |
| rs545884305 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147938360 | CATGTACCCCTGAAC[C/T]TAAAAGTTAAAAAAA | 79658 |
| rs545884976 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147796937 | GAGCCCTTCCACGGA[C/G]GCTTGTTGATTTTAG | 79658 |
| rs545885079 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148020962 | CCAAGATAAGTGTAA[A/T]ATAGCTGTAGAATAC | 79658 |
| rs545893519 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147904765 | AATGGGATTGCTGGG[C/T]CAAATAGTATTTCTA | 79658 |
| rs545897779 | in-del | -/A | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147823756 | GCAAGACCCTGTCTC[-/A]AAAAAAAAAGAAAAA | 79658 |
| rs545904891 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147890846 | AAAACAACAAAAAAA[A/C]CCACAAGTGGCCAAT | 79658 |
| rs545905225 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147922411 | AAAAAAAAAGTTGGC[C/T]GGGCGCGGTGGCTCA | 79658 |
| rs545921029 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147813031 | TAATAATGAGTGTTC[A/C]AATTTCTTTATGTTG | 79658 |
| rs545921749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148013761 | CCAAAAGAAAAATAG[C/T]ATTCACGTTGGAAAT | 79658 |
| rs545936645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147772172 | TGCGCACTGGGACGT[A/G]CCATCTCCACCTTTA | 79658 |
| rs545941509 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147905554 | TTGTAGATATGCGGC[A/G]TTATTTCTGAGGGCT | 79658 |
| rs545942076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147929947 | CATTTGTGCATACAC[A/G]TGTGTGTATATATAT | 79658 |
| rs545950865 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147777952 | AGGCACGTTGCAGGT[A/C]CAGCCAGTGTGTAGT | 79658 |
| rs545950945 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147771483 | AAATATACTCTTTTA[A/T]TTTAAAATGTATGAT | 79658 |
| rs545951181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147764104 | ATCAAAATCAGCTGA[A/G]TAGAGTTGGATAGGT | 79658 |
| rs545988196 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147873459 | GGGGGGAAATGAGGG[G/T]TGATGAGGGTTGGAA | 79658 |
| rs546002817 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147985196 | GCTCTGGCTGCAGAT[C/G]CAGGCAAGTGGGTGC | 79658 |
| rs546006444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147777462 | GAGATGGGGTTTCAC[C/T]GTGTTAGCCAGGATG | 79658 |
| rs546010906 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147959085 | TAGCATAAGCAACTT[C/T]AGATGATTTATCTTC | 79658 |
| rs546015899 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148026543 | TTTCTTTGCAATATA[A/T]GATTAAATGATATTA | 79658 |
| rs546021721 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148027387 | TCTTACTTGGGTATC[A/G]TCGGGTTGGCACTTT | 79658 |
| rs546026625 | in-del | -/CC | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147914567 | GCGCTCCCCCCCCCC[-/CC]TTTTTTTTTTTAACA | 79658 |
| rs546032996 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147998161 | GAGAAAAAAAGTAGC[A/G]TTTATGAATCCTAAA | 79658 |
| rs546034663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147817590 | CATCTCAAATATAAC[C/T]CCTCATCTCTCAAAC | 79658 |
| rs546037389 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147904320 | ACGTGCCATGCTGGT[A/G]TGCTGCATCCATTAA | 79658 |
| rs546054503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148020352 | TTGCAGGTTTGTTAC[A/G]TGAACGTGTGGCATG | 79658 |
| rs546060275 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147795352 | ACGTTTGTCTTTTTA[C/T]ACCTCCTCTCCCTTT | 79658 |
| rs546062995 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147989837 | GACATTAAAGCAAAG[A/C]CAGGCATAGGAAATC | 79658 |
| rs546063798 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147999612 | TCGTCGTAATGGAGC[C/T]GAACACTAGTCACTG | 79658 |
| rs546075978 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147933830 | GTATCTGCTGTGGGG[C/G]AGAGGCTGGAGAGCC | 79658 |
| rs546079730 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147862779 | CTGATGCTGGTATAA[A/G]TTTCTTCAAGAGCCT | 79658 |
| rs546089077 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147990076 | TGATATTCAGCCTTC[C/T]GCCTGAATGAGGAGG | 79658 |
| rs546089113 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147738573 | CCCAAAAAAAATTAT[A/T]ATACGACCTACTATA | 79658 |
| rs546104182 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147865571 | AGGATATTTCATGTG[A/G]ATTTCAGCAAAAAAA | 79658 |
| rs546105445 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147785830 | TAAATAATTATAAAG[C/G]CATAGCTCATAGTTG | 79658 |
| rs546106501 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147997267 | GGGAAAAATGTAAAC[G/T]GTACATCAATAATCT | 79658 |
| rs546121399 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147902775 | GGAAGGGAGGTTTAA[A/T]TGACTTAGTTTTGTA | 79658 |
| rs546125318 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147878961 | TTTTTTAGTAGAGAT[A/G]GAGTTTCACCGTGTT | 79658 |
| rs546126111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147818695 | TGAGTTTTATGTGCA[A/G]TGATATTGGAAAGAA | 79658 |
| rs546131671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147872868 | GTATAAGTAGATCCA[C/T]AAAGTTCAAGCCTGT | 79658 |
| rs546131806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147894204 | GCAATTAAGGTTACA[A/G]AGTAATTTTACCCTC | 79658 |
| rs546178450 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147978293 | CATTCCCACCAACAG[A/T]GTATAAGCATTCCCT | 79658 |
| rs546188325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148069820 | CCTTGCCACTCAGGC[C/T]CCCACATTGTTACAA | 79658 |
| rs546195551 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147751161 | TCCAGCCTGGGCAAC[C/T]GAGTGAGACGCCACC | 79658 |
| rs546207575 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147854282 | CATTGGATTTTTCAG[C/T]AGTTCCAGAGAAATC | 79658 |
| rs546222940 | in-del | -/TATTA | 0.0696718 | 0.173152 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147783957 | ACACATTAAATTGTG[-/TATTA]TATTTATATAACACA | 79658 |
| rs546223167 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147946092 | GACCGAAATTTTTAC[C/T]GTGGGCATGTATAGG | 79658 |
| rs546245393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147820194 | AAACTGGAGTGAGTT[C/T]GGCATGTGTGAACCA | 79658 |
| rs546248627 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147987590 | CTCTGGGTCTGCTGC[C/T]GACACAGAGCTAAGC | 79658 |
| rs546293371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147938866 | AGTAAATATAAGTCA[C/T]ATTTTTTGGAAGTCA | 79658 |
| rs546306150 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147861150 | CAGGCACGGAGTGGC[A/G]AGGAGTTCGTGAGTG | 79658 |
| rs546308504 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147819569 | TTATTTTTTCTTGAG[A/G]TGGAGTCTCGCTCTG | 79658 |
| rs546322060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147813252 | TATACCCGAGTTGTC[A/G]CTCATGGCCTCTGCT | 79658 |
| rs546334896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148035749 | CCGTGCTGAGAAACA[C/T]AGTTAGCTTCTTTCC | 79658 |
| rs546342850 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147867275 | CTTGAATATTTTCCT[C/T]TGGAAAATGTGTGCT | 79658 |
| rs546344274 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147781839 | CAAAGTACATCTTTA[C/T]GCGTCAGTATTTCCA | 79658 |
| rs546354636 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147905740 | TGGTTCCATATGAGC[C/T]TTAAAGTAGTTTTTT | 79658 |
| rs546356985 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147769648 | AGATGACATTCTACT[A/C]ATTGTAACTTTAATG | 79658 |
| rs546363009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147958407 | CAAGTTAGTTGGGAA[A/G]CAAAATGATTACCAC | 79658 |
| rs546365388 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148071397 | AAGGCGAGTGGATCA[C/T]CTGAGGTCAGGAGTT | 79658 |
| rs546390629 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARHGAP10 | GRCh38.p7 | 4:147731109 | CCTGACCTCAGGTGA[C/T]CTACCCGCCTCCGTC | 79658 |
| rs546393264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911467 | TCCCGGGTTCACTCC[A/G]TTTTCCTGTCTCAAC | 79658 |
| rs546395477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147985460 | TGGCTCTGTCTGCAC[A/G]CCTCATTGCCCAGAT | 79658 |
| rs546396389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148043245 | TTTTCTCTTCTAATC[A/G]GCGGTAGTTCATTTT | 79658 |
| rs546405228 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148042540 | GCTTTTTCCTTGAAA[C/T]TGGCAATAATTTCTT | 79658 |
| rs546421180 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147827103 | CAATAATGAAATTAG[A/T]AAAAGTTGAAAAGTT | 79658 |
| rs546423535 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARHGAP10 | GRCh38.p7 | 4:147730300 | TTGAAGAAGTCTCAG[C/G]AGCCCCTCTATGAGA | 79658 |
| rs546436273 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147873411 | GTATGGCATGCACAT[A/G]TATGCATATGTGTAT | 79658 |
| rs546453274 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147737772 | CTTGAGCCAGGGTGG[A/G]GACCCAGACAGGCTT | 79658 |
| rs546478645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147826167 | GCTCTACAGAAATAG[C/T]GTGTGACCATTGTTA | 79658 |
| rs546480141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147916644 | GGAGCAATTTCTGTG[A/G]CTCTGTAGCAGAAAC | 79658 |
| rs546483576 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148003164 | TTTCTGCCTTCATTT[C/T]GTTATGTACCCAGTA | 79658 |
| rs546484186 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147826538 | GCCACAGCCAACCAC[A/G]GAATTAACAGGACAC | 79658 |
| rs546486294 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147849577 | CAGAATTTTTAGATA[C/T]GGGGGTCAACATTTT | 79658 |
| rs546487152 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148035452 | TCTTGAGAAGTCACA[G/T]TTTTCTTTTTCTAGA | 79658 |
| rs546487273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147786097 | ATGGTTGCTTTTTTG[A/G]TTAAAAGTAAGACAG | 79658 |
| rs546489312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147959406 | AAGTTCTAGAGTACA[C/T]GTGTACAACGTGCAG | 79658 |
| rs546505478 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147916339 | ATAAACATAAACTCA[A/G]AAGACTACTGTGACA | 79658 |
| rs546506471 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147744768 | TGGATGTGGAGGGCA[A/C]GGTATTTCGTAGTAG | 79658 |
| rs546508321 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147785316 | CTCCAATCCAGTGCT[A/C]CATTTTTGCTTCTTT | 79658 |
| rs546509415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147833378 | TGCCACCATGTAAGA[C/T]GTGCCCTTCTTTCCC | 79658 |
| rs546520815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147964757 | TAGCAGCTGTCCGTT[C/T]TGTAATATAAACCAA | 79658 |
| rs546521267 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148050048 | CTTTTCATATTTTTG[G/T]TAGAGATGGGGTTTC | 79658 |
| rs546541742 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147774017 | TGCCACTCCAGCTTT[A/G]TGATCTCAGGCAAGT | 79658 |
| rs546548594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147792197 | TTTTCCAGTATTTTG[C/T]ATTGTGAAACTTTTG | 79658 |
| rs546551325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147939540 | TACAAATTGGATTGG[C/T]ATTCATTTCAATGTA | 79658 |
| rs546561643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148029434 | TTTCATAAGTGAATT[A/G]TAACTACTCTGTCTT | 79658 |
| rs546564506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148041830 | ATTTGCAAAAGAACA[C/T]TGTGTTGTATTTAAA | 79658 |
| rs546568402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148049712 | TAATATTTGCCTTTT[A/G]GTATTATTTGATATT | 79658 |
| rs546589589 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147840405 | CACTCACATGAAACA[G/T]CTAGTTTTTTTTATT | 79658 |
| rs546598181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147765888 | TCCCATTTTGGAGAT[A/G]CACAATGCTGTGATT | 79658 |
| rs546605129 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147875599 | TAACCCTGCCTCTCT[A/G]TCATCTTAAGGTCAA | 79658 |
| rs546627488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147993301 | ATTTTAAGGGTGGGA[A/G]TATAGATGAACTAAG | 79658 |
| rs546630155 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147948952 | GCCTAGGAGACAGAG[C/T]GAGACTCTGTCTCAA | 79658 |
| rs546631125 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148063901 | GTGCCTTTCTTGGGG[C/T]GGAGGCAGGGTGTAA | 79658 |
| rs546644080 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148022928 | ATACTTGTTTTTACT[C/G]TTTTATCCTGGCTGC | 79658 |
| rs546648027 | snp | C/T | 8.3999e-05 | 0.00648016 | stop-gained, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147875030 | TTTCAGACACGGAAT[C/T]GATTTGAAGGAACAA | 79658 |
| rs546661482 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147896755 | TGGGCATTTGAATCT[A/G]TAAGTTTTCTCCTAA | 79658 |
| rs546665398 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147954748 | GATAAAATAAACTAC[C/T]TTATGTAACTTGTTT | 79658 |
| rs546668542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147899299 | TCCACCATGGATGAA[A/G]GCAGCTGGGGTGTGT | 79658 |
| rs546668581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147891269 | AATAAAAGGTGGTAT[A/G]GCCATATGATGAAAA | 79658 |
| rs546690945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147999769 | CCACCATTTTGGAAG[C/T]GGCTGGTCACCATCT | 79658 |
| rs546693758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147779937 | CACTTACACCCTTAT[A/G]GTCTTGCCCGAGTAT | 79658 |
| rs546694604 | in-del | -/TTATTTCTAAATACAGTCACAT | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147937400 | TTTTTTTTCAAGACC[-/TTATTTCTAAATACAGTCACAT]TTGGAAGTACTGAGG | 79658 |
| rs546698368 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147905094 | GTTTGTTTTTTTCTT[C/G]TAAATTTATTTGAGT | 79658 |
| rs546699417 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147999174 | ACTTAGCTCACACCT[A/G]ACCAATCAGGTAGTA | 79658 |
| rs546709085 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148024727 | TGATCCTAGCTAACT[G/T]TTTTATTCTGTCTCT | 79658 |
| rs546725568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147967415 | GGAGAAATTGGGGAA[A/G]GGTAAACTCTTCAAA | 79658 |
| rs546733711 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147992477 | CAATGGCGCTATCTC[C/T]GCTTACTGCAACCTC | 79658 |
| rs546737296 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147998494 | AAATTCTTTTTGTGA[C/T]GTCAGCAGGGCACTA | 79658 |
| rs546754573 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147867699 | TGAAACCCTGTCTCC[A/G]CTAAAAATACAAACA | 79658 |
| rs546755585 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147972975 | GGCCAGGCTGGTTTC[A/C/G]AACTCCTGATCTCAA | 79658 |
| rs546763599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147753373 | TTTTTTTTTTGAGAC[A/G]CAGTCTGTTGTCCAG | 79658 |
| rs546766400 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147922083 | TCTGCAGGGCAAGAG[A/G]AATTGTCCAGGTTTG | 79658 |
| rs546767914 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147746049 | CGCCTCTGCCTCCCA[A/G]AGTGCTGGGATTACA | 79658 |
| rs546774254 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147962966 | GTGCCTGGCCACCAC[G/T]CCTTTCATTTCTTTT | 79658 |
| rs546797208 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148033640 | ATTTATATGTGTTTA[C/G]TTTACAAATGTTTCA | 79658 |
| rs546808220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147787590 | GCAGTTTGTTGAGTC[A/G]GATGGGATTAGAATG | 79658 |
| rs546811112 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148066307 | AGTATGCAGAACTGA[A/G]TCACATGCTTACCCT | 79658 |
| rs546813282 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147778190 | ATGCCTGCTCAGACA[G/T]GATTTTTGCATGTGT | 79658 |
| rs546828114 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147738360 | ATCGAGACCATCCTG[C/G]CTAACACGGTGAAAC | 79658 |
| rs546844500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147785543 | CATGGGTGTATGTAT[A/G]TGATATCTAGGACAT | 79658 |
| rs546868905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148057199 | TGGCACTCAGCCAAC[A/G]ATGATAGTGCCAGCT | 79658 |
| rs546870424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147745522 | TTTGAGACGGAGTCT[C/T]GCTGTGTCACCCAGG | 79658 |
| rs546870590 | snp | A/G | 1.6591e-05 | 0.00288015 | synonymous-codon, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147879242 | TGAAGGGCCTGCTCC[A/G]TTTGGTTCCAGTTGG | 79658 |
| rs546879714 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147933454 | TAGCTGTTTATTTTC[A/G]TCTACCCAGTCTGGC | 79658 |
| rs546884377 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148064161 | ACCAGGTAGGGAGGA[G/T]AATTAGGTGAAGTGG | 79658 |
| rs546884405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148070615 | ATCTATGGGGAAAAA[A/G]AGAGTAGAATACAGA | 79658 |
| rs546885359 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147833087 | ATCCTGGATACAAGA[A/T]TGGAGCTCCTTAAGA | 79658 |
| rs546896558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148064585 | GGAGTGAGCAGTCAG[C/T]GATGGTGCTGTTGTC | 79658 |
| rs546910200 | snp | G/T | 0.000448467 | 0.0149677 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147965157 | TTCTTCGTTTTAACT[G/T]TCTTCACTTTGCTCT | 79658 |
| rs546913708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147971704 | ATTGGAAAGAGATTC[A/G]GGCCAGGTGTGGGAG | 79658 |
| rs546917148 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147972363 | CATTGCATAAATATA[C/T]GTAATAGTATCCCTG | 79658 |
| rs546926450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147906455 | GATGGTTATGTAACA[C/T]TGTGAACATATTTAA | 79658 |
| rs546927265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147940043 | TGCTGAGCAGAGACA[A/G]TTGACCCACAGAAGT | 79658 |
| rs546935566 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147848303 | TTAATGAAGGGCTAC[A/G]AATTGAGGCTCAGAC | 79658 |
| rs546935837 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148035597 | AGAGGGAAAATGAAA[C/T]GGGAGGAGTGAGGTC | 79658 |
| rs546939146 | snp | A/G | 1.64857e-05 | 0.00287099 | synonymous-codon, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148023277 | GATTTTTCGGACGCC[A/G]CCCGATACTACATTC | 79658 |
| rs546945118 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147844983 | AGAGCCCACAAGGCC[C/T]GGCACGCTCTGATCC | 79658 |
| rs546945950 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147849897 | GCTTGCTAGGTTCTA[C/G]CTTTTGTTCAAAAAG | 79658 |
| rs546947419 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147977583 | CATAGACAGTTTAGT[A/G]TAATATGGCATAGTA | 79658 |
| rs546954861 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147862357 | GGGGCAGTGGGCCTT[C/T]GCCGGCCCCCAAGAG | 79658 |
| rs546955792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147919659 | CTCAGTGCAGCCTCC[A/G]TCTCCGCCTCCCGGG | 79658 |
| rs546956597 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147744995 | ATCTTTTAAGGGGTA[A/G]GTGAAAGAAGAACTT | 79658 |
| rs546968617 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147912182 | ATTTTAAAATTATTT[G/T]ACATTACAAATATGT | 79658 |
| rs546969198 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147780388 | ATTACTGGGAGTGAC[A/G]GTAGCCCCGCTAAGG | 79658 |
| rs546986569 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148018557 | AGAGACCATCAGAGC[A/T]TGGCTTTGTATCCAC | 79658 |
| rs546988480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148010914 | TTGCCCCAATCCAGG[A/G]TCATACATTATATTT | 79658 |
| rs546993339 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889211 | CTAGTGTCTTCATTC[G/T]GCTTCAAGAAAAATA | 79658 |
| rs546997187 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147954169 | GGGAATGTGTGTTCT[C/G]CTTTTGAGTGGAGTG | 79658 |
| rs547002187 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147947287 | TCAGGGTTAGATGAA[G/T]AACAAGTATATAGAC | 79658 |
| rs547006416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147979752 | GGACATCATTCACTT[C/T]CTTGGTTAAATATAT | 79658 |
| rs547023658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148011706 | AGAGAATTTGTGGCC[A/G]TGTTTTAAAATTGCC | 79658 |
| rs547024688 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148037600 | AACCCTTTGGGAGGC[A/C]AAGGCAGGGGCGGAT | 79658 |
| rs547037515 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148004612 | TGGCAGGAAACCGCA[A/G]GCATCCTCTAGGAGC | 79658 |
| rs547049536 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147836558 | CCATTTCCTATTAAT[C/T]GGCTCCTGATTTTCA | 79658 |
| rs547056526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147801762 | TTTCATCAGGTCATC[A/G]CTGTTTACTCCACAG | 79658 |
| rs547065297 | snp | A/T | 0.0295035 | 0.117819 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147887875 | TCAAAAAAAAAAAAA[A/T]TTTTTTTTTTCCTAT | 79658 |
| rs547071768 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147788914 | TAAAACCAGGTTTTG[G/T]TTGAAACATCAGTTA | 79658 |
| rs547082214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147927715 | GGTGAGAGGAAGAGT[C/T]GGTGGACAGTGCAAC | 79658 |
| rs547100068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147894701 | ATTTTTGGGGTATAT[A/G]TGGTGTGAGACATGA | 79658 |
| rs547105430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147918631 | CTGGACTTAGGGGCC[C/T]TTCATCTCCCTAGCT | 79658 |
| rs547107129 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147891651 | TTAAACAATGGAACA[C/T]AGCTGCAAATGAATA | 79658 |
| rs547109389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147960384 | AAATACTATTATTAG[A/G]GGTGTAAACTGGAAC | 79658 |
| rs547110005 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147867818 | GCAGTGATCCGAGAC[C/T]GTGCCACTGCACTCC | 79658 |
| rs547111509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147739592 | AAGAAGACGACCAGA[A/G]ACATCCCTAAGAGGG | 79658 |
| rs547115792 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147828724 | CCCCTTCCTTTCCCC[C/G]CTACAATGTCCAGCT | 79658 |
| rs547122451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147966152 | TCCTTGGAAGCAAAA[A/G]TATAATATTCTGGGG | 79658 |
| rs547127627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148058766 | AGTAACCACATATAC[A/G]GCACTGTCATAATTT | 79658 |
| rs547141801 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147834589 | TCAACTTGTTTGAAT[G/T]TCCCAAGCCTTCTAA | 79658 |
| rs547145025 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147988295 | TTTTTCAGTTTTCTC[A/C]GCCCACAGTTTAAAC | 79658 |
| rs547146434 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147918282 | CTGGGACTACAGGTG[A/C]CCGCCACGAAGCCTG | 79658 |
| rs547162470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147786746 | ATTACTATCTTGAAC[C/T]TGTAAGACCTGTTAA | 79658 |
| rs547183559 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147917631 | TTAACTTAAGAGTTT[A/C]AGAAAGTAGTATGGA | 79658 |
| rs547196247 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147938528 | CCTCCCAGCATAACA[G/T]AGGGTATAGGATGCA | 79658 |
| rs547204822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147880418 | GGTGAGGAGAAGGAA[A/G]TGAGGAGATGGCTCT | 79658 |
| rs547207986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147793665 | TGAGGCTTCATGTGT[A/G]TACTGCTCAACTGTC | 79658 |
| rs547212503 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147768064 | GGATGACTTTTAAAT[A/G]TTTACACTGAATAAA | 79658 |
| rs547213889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148016225 | AAGAATTACTGGAGC[C/T]GGATGCAGTGACTCA | 79658 |
| rs547215575 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147934829 | CAGAATGAGACCCTG[A/C]CTTAAAAATAAAAAA | 79658 |
| rs547225617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147754078 | GCAGTGTCTGTCTTT[C/T]GTCCTCCAGCAGTGT | 79658 |
| rs547245569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147886510 | CTACAGTCTGTTGTT[C/T]GTCGTGCACTCACTT | 79658 |
| rs547250684 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148009476 | AGTCTTGAGGTAAAA[A/C]ATGTTAAGATCCTCT | 79658 |
| rs547260533 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148031697 | CATTTAAAAAACAAA[A/T]GTTTAGTGTTGTAAG | 79658 |
| rs547270542 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147993845 | CATTCTAGTCTGCTT[C/G]GGGGAGAGGGTAGGC | 79658 |
| rs547273844 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147868215 | GCAGGTAGTAGAATA[C/T]TGAGTCTAATGTTGT | 79658 |
| rs547275287 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148015628 | AGAGAGTCGGAAAAG[G/T]TTTTCATTGCTTTCT | 79658 |
| rs547275810 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147783499 | GCACACATTAAATTA[C/T]GTATTGTATAATTTA | 79658 |
| rs547306631 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147987495 | GTATTTCCTTCAGGC[A/G]ACAGCCCAGCAGCAC | 79658 |
| rs547309760 | snp | A/G | 4.96627e-05 | 0.00498286 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148072067 | ATTCCACAGAACTAC[A/G]TCAAGCTGCTGTAGC | 79658 |
| rs547310146 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147932622 | ACATGGACACATGGG[A/G]GGAACAACACACACT | 79658 |
| rs547315057 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147745645 | TACAGGCGCCCACAA[C/T]CACGCCCTGCTAATT | 79658 |
| rs547320274 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148008912 | TTAAGTCGGACGTTA[A/C]AGAGATTTGCAAAAT | 79658 |
| rs547322914 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148053186 | ACAAGCAGTAAAGGA[A/C]AGGTGAGTTTGACCC | 79658 |
| rs547327319 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147891969 | TGACCCCCCCACACA[C/T]TTGCTTGATAAATAA | 79658 |
| rs547356513 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147771941 | GGACAACAGGCGTGC[A/G]CCACCACGCCCAGCT | 79658 |
| rs547358668 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147936362 | AGTCTTGCTCTGTCG[C/T]CCAGGCTGGACTGCG | 79658 |
| rs547367304 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148020380 | ATGCTGGTTTGCTGC[A/C]CGTATCAACCCATCA | 79658 |
| rs547367361 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147883037 | TGCTGCTTCCTCTCT[G/T]AGATGATATAGTTGA | 79658 |
| rs547372372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148060933 | GACTGCTGATTCTGT[A/G]TTCCTGTTTTGGGAT | 79658 |
| rs547377866 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147970583 | CTAAGAATGTGAAAA[A/T]TGTTGACTCCAGGAA | 79658 |
| rs547382504 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147968398 | GCAGTACTTTTCAAT[C/G]TTCTTGGGATCACAG | 79658 |
| rs547390854 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147906827 | GTTCCCTTCTATAAC[A/C]GGTATTCCAAAAATC | 79658 |
| rs547403832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147851130 | GCCAATTATAATTTT[A/G]TCCAAATAGAAGAAG | 79658 |
| rs547416826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147968927 | TGGGACTCGGATCCT[A/G]TAAACGTACCCCAGT | 79658 |
| rs547418833 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147962054 | AACATTTCTAGCCTT[G/T]ATCTCTAAAGCCTCC | 79658 |
| rs547419525 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911653 | AGGCGTGAGCCACCG[C/T]GCCTGGCCTCTTAAC | 79658 |
| rs547421869 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147770554 | CTGTATCACATTGTT[C/T]TATGGCTATATCTCT | 79658 |
| rs547423827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148067159 | TGTCTTGTAGGTGCC[A/G]CCCTGATTCTTTTGC | 79658 |
| rs547437937 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147755454 | CTTGAACTCAGGAGG[C/T]GGAGGTTGCGGTGAG | 79658 |
| rs547451312 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148025975 | CTTCTCTCTTCCCTG[C/T]CCCCGCCCCGTGACT | 79658 |
| rs547454848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147754649 | CTTTCACCAGCTAGA[A/G]AATTTGGGTGAAATT | 79658 |
| rs547464862 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147805731 | GAGGTAGGAGGATCA[C/G]TTGAGATCAGAGTTT | 79658 |
| rs547470021 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147910985 | TTTTCTTCTTCTGAC[A/T]CCTTTTCTTCCTTCC | 79658 |
| rs547477911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147747390 | TCTCTTGCTCTTTTC[C/T]AGCTAACTACTTAGG | 79658 |
| rs547481124 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147887285 | GCTGCCTGTGTTCCT[A/G]ATGGAGGCCAACTCC | 79658 |
| rs547488377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148019759 | GACAGAGTGAGACTC[C/T]ACCTAAAAAAAAAAA | 79658 |
| rs547521732 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147802674 | CTCCCTGTAACTTCT[A/C]CTTACACTGGTTTTT | 79658 |
| rs547522078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148066557 | GTGTGCGTGTACACA[C/T]GTACACATACATAGT | 79658 |
| rs547527039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148033221 | GCTGTATAGTACTCT[C/T]TGCATTCTATTGTAT | 79658 |
| rs547534372 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147809480 | TCATTATTTTCCTTC[A/C]CTGCAATTCAACATG | 79658 |
| rs547536612 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148040523 | TTTTTTGTATTTTTC[A/G]TAGAGACTGGGTTTT | 79658 |
| rs547543503 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147882538 | GAAGAGAACAATGGC[A/G]AGAGGAACTGGGTGA | 79658 |
| rs547551910 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148039061 | CACCCCCACCATGTT[A/G]GTATTTTCCAGAATT | 79658 |
| rs547555041 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148023980 | TCTCACGTCCCTTCC[A/C/G]AGCCATGCTGTTCAG | 79658 |
| rs547571280 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147850013 | GATTGTAAACGCACC[A/C]ATCAGCGCTCTGTAT | 79658 |
| rs547577034 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147786668 | ATGCAGGTCGTGCAT[A/G]TGGGATGGCATACAT | 79658 |
| rs547587323 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147748886 | ATTGCTTGAATCCGG[A/G]AGATTGATGCTGCAG | 79658 |
| rs547593454 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147941806 | TGCTACCAATACAAA[C/T]CTTAGCCCTTGACAA | 79658 |
| rs547595883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147902369 | AAATTAAATCCTTAG[C/T]ATGGTGTATTAATTC | 79658 |
| rs547603753 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147880996 | AATTAACATTTGGCC[A/G]GGGACACTGGCTCAC | 79658 |
| rs547620408 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147823562 | CAGGAGTTCGAGACC[A/C]GCCTGGCCCACATGG | 79658 |
| rs547620582 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147858737 | CTGCAGCTTTTACAG[A/G]CCCCCTTTATGCTAG | 79658 |
| rs547629607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147908540 | TGTATTTATATGGGG[A/G]CACTGAAGGGACTGC | 79658 |
| rs547635913 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147955544 | GAGGTGAATAAAAGG[A/G]ACAGTATATTCTTTC | 79658 |
| rs547646335 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148065060 | GAGGATTTAATATTC[A/G]TACACAAGCATTTAG | 79658 |
| rs547678837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147859376 | CTGCCGGATTCAAGC[A/G]ATTTTCCTGCCTCTG | 79658 |
| rs547692455 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147814224 | TCTTGTGGTTCATTT[A/C]GTTCTTATCATCGTG | 79658 |
| rs547715562 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147920742 | GCACCGATTAAGAGA[A/C]TATGAGTGCATGTTG | 79658 |
| rs547715671 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147789420 | TCAGCCTCCTGGGTA[A/G/T]CTCGTATTACAGGCA | 79658 |
| rs547716343 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148030883 | AAAGAAAAAAAAAAA[A/C]CATTTAAGCCTATTA | 79658 |
| rs547726318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147851911 | GAGTTAATTCTTCCT[A/G]GTTTGAATCCTCTTT | 79658 |
| rs547733753 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147821479 | TTTACAGTTTTGCCT[C/T]TTCATATTTAGGTCT | 79658 |
| rs547734199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147770851 | TTAAATAGCAGTCTT[A/G]TTTTCTAGTAATTCT | 79658 |
| rs547755136 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147803256 | TCAAGTGATTCACCC[A/G]CCTTGGCCTCCCAAA | 79658 |
| rs547770560 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147814784 | TCTTTTTATAAGAAC[A/G]CAAGTCATATTGGAG | 79658 |
| rs547772693 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148068689 | GCTACTGGTTGCCTC[A/G]GGGTGGGAGATAGGA | 79658 |
| rs547777026 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147859512 | CTCCTGACCTCAGGC[A/G]ATCCACCCACCTTGG | 79658 |
| rs547777074 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147932147 | TCAGAATGGCTATTA[C/T]TAAAAAGTCAAAAAA | 79658 |
| rs547777566 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147763597 | TTACAGGTGTGAGCC[A/C]CTGCGCCTGGCCTGG | 79658 |
| rs547791700 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148026665 | CTAGTTTTCTTAAAT[A/T]AGAGCAGCTGTTAAA | 79658 |
| rs547800842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147872963 | GCACACTGTGCCCAG[A/G]TCTTGTCGCAGGAGT | 79658 |
| rs547803195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148046823 | AATCAAGTAACACCA[C/T]ATAATTATTAGTGGA | 79658 |
| rs547804522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147865985 | TAGAAGTAGAGAAAG[A/G]CTGAGTAATTTGCCT | 79658 |
| rs547806803 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147852550 | GGTGTGCCTTCTCCC[C/T]GCTGGAGTGGGGAGT | 79658 |
| rs547807406 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147885387 | ACTGCCCTTTATAAA[A/G]ACTATCAGATCTTGT | 79658 |
| rs547809088 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147815712 | AAATAAAAAAATAGG[C/G]GATAGGCGTGGTGGT | 79658 |
| rs547823916 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147962563 | ACGGTCCTGACATAC[A/G]ATCTTTTGACTTTAT | 79658 |
| rs547831517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147903782 | TCTTCTCATGGCTCA[A/G]TAGCTCATTTCTTTT | 79658 |
| rs547831883 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | ARHGAP10 | GRCh38.p7 | 4:148073111 | GCCCTGGGACCAGCC[A/G]TCCTACCAGCACCAT | 79658 |
| rs547832888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147737419 | CTCGGCCTCCCAAAG[C/T]GCTGGGATTACAGGT | 79658 |
| rs547856560 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147896317 | AATTCACCTATGAAG[A/T]CATCTTTGCCTAGAG | 79658 |
| rs547881768 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147901396 | AAGTGTGAAGTGTTC[C/T]GAAGAATGTAGACTG | 79658 |
| rs547886293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147909032 | CCACAAGACTGCCTG[A/G]GTTCAGGTGCCCATC | 79658 |
| rs547887197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147996069 | GGGGGCCTGTATGTG[C/T]GAAATACTCAAAAAG | 79658 |
| rs547887645 | in-del | -/T | 0.406641 | 0.194842 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147912645 | TACATAGCCTTAAGC[-/T]TTTTTTTTTTTTTTT | 79658 |
| rs547888865 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147989313 | AAACGAAATTAAAAT[A/T]GCTAATGAAGTTTTG | 79658 |
| rs547900314 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147951008 | AGGTGGCTCAAAAAC[A/G/T]TGTCGGGTGGGAGGC | 79658 |
| rs547914429 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147912837 | ATCTTCAGTAGAGGT[A/G]GGGCCTCACCATGTT | 79658 |
| rs547919214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147950067 | AACAAACATTGCCTA[C/T]AGAACGACATTATGA | 79658 |
| rs547920058 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147744419 | GCCCTTGGAAAGCAG[A/G]TTGAGGGCTTTACTC | 79658 |
| rs547920393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147964376 | TTTGCCCGCATTCCC[C/T]GTTCTTCCTCTGCCT | 79658 |
| rs547924020 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147989889 | GTGATAAGTGTCCAT[A/G]AAATCTTTACAATTT | 79658 |
| rs547926837 | snp | C/T | | | upstream-variant-2KB | ARHGAP10 | GRCh38.p7 | 4:147730871 | GAACTATTAGTGTTT[C/T]TTTTTAAGAAATACT | 79658 |
| rs547938064 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147957459 | TCTCCCCTTTTGAAT[G/T]CTGTTGGAAAATCGG | 79658 |
| rs547938296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148044830 | ATACATTAAAAGGAA[A/G]TCATAGCAGTGGTCT | 79658 |
| rs547938997 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148047235 | TTCCTTGAATACTGT[C/G]TGTGTTTCTAGTATG | 79658 |
| rs547946593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147970272 | GACCTAAGTATACCC[C/T]TCAGAGGATCCTAAC | 79658 |
| rs547951661 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147769294 | GTAATTAGGGAAATT[A/C]CTCAGTAAATGTTGT | 79658 |
| rs547952878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147838909 | CTGTTTGTAATCTCT[A/G]AGTATCTGAAACTAA | 79658 |
| rs547956087 | snp | A/T | 0.000148538 | 0.00861667 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147864853 | TAACATAGGCAGATA[A/T]CCAAGTAGAGCAGAA | 79658 |
| rs547957159 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147956763 | TCCTTTTTTTTTTTC[C/T]TTTATTATTATACTT | 79658 |
| rs547966091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147775961 | GCATAGAAAAGTTCC[A/G]TAAGCTGGCTATGAT | 79658 |
| rs547971243 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147949017 | ATCCATTGTAGTGGT[A/G]GTATATTCTTTCTGT | 79658 |
| rs547981884 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147996722 | TGTTGAAGCCCTAAC[A/T]TTAACCATTGTAACT | 79658 |
| rs547982578 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147735598 | AGGAATGTGGACTTT[A/T]TCTTGTGGAGAGTTA | 79658 |
| rs547985867 | in-del | -/A | 0.0221141 | 0.102801 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147854608 | ATGCAGTATTGGGGG[-/A]AAAAAAAAGCTCCAT | 79658 |
| rs547986534 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147781746 | GCAGTGGCGCAATCT[C/T]GGCTTAGTTTTCTTT | 79658 |
| rs547991912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147864309 | GTCCAGCCCTGGCCC[A/G]CCTTTGAGAGCCGGG | 79658 |
| rs547995070 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148015873 | ACTTAGGAGAGCCTG[C/T]GTTGATTTCTAGCTG | 79658 |
| rs548007269 | in-del | -/A | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147922390 | ACCCTTAGTTCCTTT[-/A]AAAAAAAAAAAAAAG | 79658 |
| rs548009086 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148001383 | TTTGGCTTAGGATTG[A/T]CTTGGCAATGCGGGC | 79658 |
| rs548016629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147736856 | TTCTGACCAAGGAGA[C/T]GTGACAGGAAGTCTG | 79658 |
| rs548024360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147775556 | GCCTGGTAGGAGAAA[A/G]GTGATTATTGTCAGT | 79658 |
| rs548027664 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147876808 | CACTGTGCTAAATTC[A/G]TATACAACTTGTCTC | 79658 |
| rs548032569 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147871380 | TTTGCCCCCCAAGTA[G/T]GACTATTCGTGTCCG | 79658 |
| rs548033179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148055576 | CACCTGTAATCCCAG[C/T]TACTCGGGAGGCGAA | 79658 |
| rs548037215 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147825154 | CTGATTTGGATTTAA[A/T]AAGTGACAGAGGGCT | 79658 |
| rs548048366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147995739 | CTTTTTTTTTCATGA[C/T]GGAGTCTTGCTCTGT | 79658 |
| rs548055224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147750599 | AAGTACATATAAAAT[A/G]TCTTTTTTTTTTTTT | 79658 |
| rs548062523 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147845498 | GCAACTTTGGAGAAG[C/G]ACCTCTTTGGTACTT | 79658 |
| rs548063207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148046283 | TTAAAAAAAAATTTA[A/G]CTTTGGTTTAAATTC | 79658 |
| rs548065199 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147830660 | GAGCAGCTGGGACTA[C/T]AGGCACTTGCTACCA | 79658 |
| rs548068438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147749925 | GCCATGTATCCAGAA[A/G]CAGAATGTATCACTT | 79658 |
| rs548069899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147783154 | CACACATTAAATTAT[A/G]TATTGTATAATTTAT | 79658 |
| rs548075106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148067764 | CCTCGTCAGTAGTTA[C/T]GCGTTTGGGATGTGT | 79658 |
| rs548077384 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147837172 | GGGGAAGGTATAGGC[C/T]GGGGGAGGCTGGATA | 79658 |
| rs548079390 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147817439 | ATAGGTGGCTCTGCT[A/G]TAAGAAATAATTTTC | 79658 |
| rs548091799 | in-del | -/TTC | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148014312 | ATTTGGGGAAGTGTA[-/TTC]TTCTGACTTCAGAAA | 79658 |
| rs548118122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147936946 | GTCAGATCAGTGGCG[A/G]CATTAGATTGTTATA | 79658 |
| rs548121912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147845011 | TCCCCTGCCATCACT[C/T]AGCATTACAGGCTCA | 79658 |
| rs548147040 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147741758 | CAGGCATCTTGATAT[C/T]GTTCTCTTTACACAC | 79658 |
| rs548147179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147962530 | ATCAGTTAGAAGCAA[C/T]GACTCCCAGGTGTAG | 79658 |
| rs548165963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148008440 | AAGGGGACATTTGGT[A/G]GTGTCTAGAGACAGT | 79658 |
| rs548180776 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147976246 | TCTCTTTAAAAAACA[G/T]CTAGCCAAAAATGCT | 79658 |
| rs548186055 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147777109 | GACATAAATTTACAT[G/T]AATGTTAAACTGTTT | 79658 |
| rs548191847 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147958010 | ATAAAAGGAACCCAG[G/T]AGACGATCCATCTTG | 79658 |
| rs548206347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147997352 | AATCTCTATAGAACT[A/G]TTCAGTAAAATGGGA | 79658 |
| rs548213486 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148034420 | CCTCCCAGGTTCAAG[C/T]GATTCTCCTGCCTCA | 79658 |
| rs548239185 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147791768 | TTTTGTATTTTTAGT[A/G]GAGATGGGGTTTCAC | 79658 |
| rs548241885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147818147 | CTCTGAACCTATTTT[C/T]TTTTCTTCTTCTTTT | 79658 |
| rs548242038 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148050155 | TACAGGCGTGAGCTA[A/C]CGTGCCCTGCCATAA | 79658 |
| rs548249451 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147949507 | TGGTTTGCAGTGCTC[C/T]TGGCATCTGGTGGCA | 79658 |
| rs548256539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147972210 | ACATGAGATTGGCGT[A/G]AGAAAATATTTATTG | 79658 |
| rs548259093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148055995 | AGGGGTGAGCAAACC[A/G]TGGCCCACTGCCACC | 79658 |
| rs548276790 | in-del | -/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147816005 | ATAAGAAATGAATAC[-/G]TAAGTGTCAGCTGTT | 79658 |
| rs548281846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148007632 | TGCTGACACAGAACT[C/T]GCTGTCTCCCAAGTT | 79658 |
| rs548285484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147885341 | AAAGGCACATCTTAC[A/G]TGGCAGCAGGCAAGA | 79658 |
| rs548288045 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147851958 | CATGTGATTTGGGAC[A/G]AGTGACTTAAGGCCT | 79658 |
| rs548288482 | in-del | -/G | 0.238519 | 0.259481 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148040814 | TATTAAAAAAGATTT[-/G]GGGGGGGGTTATTTG | 79658 |
| rs548294416 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148049163 | ATAGATGAGTGCCTC[G/T]TGGACTTGAGTATGC | 79658 |
| rs548299744 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147915952 | GTATAAAAATTTTTT[A/T]AAAAAAATTAGCTGA | 79658 |
| rs548299896 | snp | A/G | 6.68874e-05 | 0.00578267 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147909756 | AGTTTTAATACAGCC[A/G]TCATCCCAAGACCAG | 79658 |
| rs548319948 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148071641 | AAACAAACAAACAAA[-/C]AAAAAACACAAAAAG | 79658 |
| rs548322865 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147792541 | CTGAGACATTACCAA[A/C]AACTTCCTGTGCTTC | 79658 |
| rs548325660 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147985308 | GCTCAGGCTACTGAT[A/C]CAGGTGAGCAGGTGC | 79658 |
| rs548328755 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148003636 | GATAGTTAGCTCTTC[C/T]TGTTGAATTGATCCC | 79658 |
| rs548334326 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148041055 | TAGGTTTCAGCGTCC[C/G]CCAGCTAGCCAAATG | 79658 |
| rs548357252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147798364 | CCTCCTTAGATTATA[A/G]ACTCTGAAGTTAGAG | 79658 |
| rs548360129 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147878051 | AAGCCATTCTTCTGC[C/T]GCACCCTCCCCAGTA | 79658 |
| rs548373232 | in-del | -/TA | 0.00716266 | 0.059414 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147766634 | ACACATATATATACG[-/TA]TATATACACACCCAC | 79658 |
| rs548382216 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147751931 | TTGCTCTGCCATCAG[C/G]TTGGAGTGCAGTGGC | 79658 |
| rs548403605 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147985850 | CTCGGCCTGGGTTGC[A/G]CGGATCCCTAGCAGT | 79658 |
| rs548405884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147790311 | TAAACTTAATCAACT[C/T]CCAGAGGTGCCACCT | 79658 |
| rs548413395 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148063970 | GAGCGGTGGCCACCC[A/G]GAGTGGATCTGGGCC | 79658 |
| rs548422143 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147854151 | TAAAAAAGGTTTTGC[A/G]TGTGCAATTTTATAA | 79658 |
| rs548442337 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148007322 | AGGGCAACCCCATTG[C/G]CATGTTCACATGGTT | 79658 |
| rs548448228 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147854105 | TCTTTTTTTTGACCC[A/C]AAATGCTGTTCTAAG | 79658 |
| rs548451526 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147991158 | CCTAAAAAAAAAAAA[A/T]AATAAATAAAAGAAA | 79658 |
| rs548470845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147796562 | GGAGTCTCACTCTGT[C/T]GCCCATGGCTGGAAT | 79658 |
| rs548476913 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147959159 | ACATAGAAATGATTG[C/T]GAATAGAAAGCTCTG | 79658 |
| rs548490772 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147976958 | AGGTGAGTTTTTGAT[A/T]CACTAGAAAGAAGAA | 79658 |
| rs548509911 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147764553 | TTTTTTTATTTTTTG[A/T]GATAGAGTCTCACTC | 79658 |
| rs548509976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147771612 | AATAGTATATGCATG[C/T]GAGCTTAGTGCATGC | 79658 |
| rs548523122 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147815383 | TGATGTCCTGTCCTA[A/C]TCATCCCTGGAACCT | 79658 |
| rs548544275 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147933533 | TCTTGGGTTTCCTGA[A/G]CCTGTGACCACTGTA | 79658 |
| rs548555130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148058037 | GGGGAGCCAAACAAT[A/G]TGCTTGCGTGTGGAG | 79658 |
| rs548563381 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148002605 | AGCCTGTTATTGGTC[G/T]ATTCGGGGATTCAGC | 79658 |
| rs548563414 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147873828 | TGTGATGAGGTATTA[C/T]CATGCCACTGTACTC | 79658 |
| rs548567029 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147927767 | GATCCTAAGGGAAGG[C/T]GCAGAGGCTGTGAGA | 79658 |
| rs548579761 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147930175 | GTTAGTTTACAGAAC[C/G]ATGGAATTTGAGAAT | 79658 |
| rs548584565 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147845930 | ACTCTTTGGTTTGCC[A/G]TTGCTGTAGGTCACA | 79658 |
| rs548604612 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147780475 | AAGAGGGCAGTGTTT[A/G]TAGAGGTGATGAAAT | 79658 |
| rs548625066 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148068793 | CGTGTGATGATGACA[A/G]TTCAGTGATTTCAGT | 79658 |
| rs548626007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147745584 | GCAAGCCCCGCCTCC[C/T]GGGTTCACGCCATTC | 79658 |
| rs548628964 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | ARHGAP10 | GRCh38.p7 | 4:147730399 | TTTGTTTACACCCCC[C/T]CTCTTCTTGTCTTTC | 79658 |
| rs548639376 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148027806 | GAGGCATGAGCAAGA[G/T]AACAGAAAACTAGAA | 79658 |
| rs548641008 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147859165 | TGTCTCAAACCTTCA[A/T]TTACTCTTCCAAATA | 79658 |
| rs548656074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147849035 | TTGCTCAGTACAGTA[C/T]GTGTGTTGACTGTTG | 79658 |
| rs548663944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147751449 | GCTCACTGCAACCTC[C/T]GCCTCCTGGGTTCAA | 79658 |
| rs548676734 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147800345 | TGTGTGCAATGGAAG[G/T]GCGTCTTAGGCCCAT | 79658 |
| rs548679274 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147840434 | TTTCTTCCTCCTAAA[A/C]CTTTTTAGCATTCTG | 79658 |
| rs548692933 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147944156 | ATATTCAGTTACTGA[A/C]GTAATTGGTTGGCAA | 79658 |
| rs548699424 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148063488 | TTCAGTAGCAAGGAC[A/G]TTCTTTGGAGAATTT | 79658 |
| rs548711041 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148063994 | CTGGGCCAGTGGTTT[C/G]TCACCTGTGGAGTGT | 79658 |
| rs548712481 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147939576 | GATACTTAACTAACT[C/T]ACTAACATTGAGGCA | 79658 |
| rs548715732 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148023643 | TTTTTATTTTTAAAA[G/T]ACAGCTTAAATTTCT | 79658 |
| rs548739730 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147797789 | CAGTCTTAACCCTGC[A/G]AAACCTTCTCTGCCT | 79658 |
| rs548740829 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148071190 | ACTTGCAAAGGCCTG[G/T]AGTTGCAGTTGGGAT | 79658 |
| rs548741656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148028298 | GACAGTTGTGAATGA[C/T]GGGCGGAACTGATGT | 79658 |
| rs548743527 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147839741 | ATTCTCTGCAGGTTG[A/G]TTGTTATTCTCAACA | 79658 |
| rs548753130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147806879 | GCTAAAGGGGCCAAC[A/G]TTTTGAATAGCATTG | 79658 |
| rs548772428 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148029570 | TCCTTGTAAACATGT[G/T]ATCAGCTTGATGCAG | 79658 |
| rs548785910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147899737 | GAAAAAATGCATGAT[C/T]CATAGATTTATACTT | 79658 |
| rs548811507 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147937838 | TACAAAATTAGCTGG[A/G]TGTGGTGGCATATGC | 79658 |
| rs548812060 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147804626 | TATAAGTGTTCCCTT[G/T]TCTCCACAGCCTTGC | 79658 |
| rs548832007 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147789717 | ACTGGCCTGCCCAGT[A/G]CACACAGCTAGGTGG | 79658 |
| rs548845444 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147870530 | ATTTTTCCCCATCTG[A/T]TAATACCTATTGTAT | 79658 |
| rs548846437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147898145 | CAAAACTGGGTTTTT[A/G]TCTTGTTCCATTTCT | 79658 |
| rs548862584 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147811602 | TTTTAAAAAAAAAAA[A/C]CAAAAAACAAAACAC | 79658 |
| rs548871918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148044175 | GATTTAATATGTTGA[A/G]TGACAATTTGTGCTG | 79658 |
| rs548884701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911140 | CACGGTTTTGCTAAG[C/T]AGAAATAAATACTTC | 79658 |
| rs548890146 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147953978 | TCGTTCTTTTCAGAA[A/T]ACTTTCTAACTTCTC | 79658 |
| rs548891302 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147786599 | AGGAAAAAAGTTTTA[A/G]TGTTTCAAAGGATAA | 79658 |
| rs548902002 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889369 | CAATGGCACGATCTC[A/G]GTTCACTGCAACCTC | 79658 |
| rs548907339 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147896389 | TTAGAGGATATAATG[A/G]TATTCAGATTTTCTA | 79658 |
| rs548945235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147999601 | AGTGCCCATGTTCGT[C/T]GTAATGGAGCTGAAC | 79658 |
| rs548964174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147760297 | TGAAGGAGGTAAGTG[C/T]GTCGGGTTACAATAT | 79658 |
| rs548987075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147955187 | TTTTTGATATGTAAA[A/G]GTATTCCCTAGGGAA | 79658 |
| rs548989418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147863169 | TTCACATTGTTTTGC[A/G]ACTGTCACCACCATG | 79658 |
| rs548989999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147843205 | CATCCCATCTCCTCC[C/T]GTGTCAGAGATTTTG | 79658 |
| rs548996503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147827838 | TTGAGATGGGGTCTC[A/G]CTCTGTCACCAGGCC | 79658 |
| rs549000070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148064609 | TGTTGTCGGGAGGGC[A/G]AGTCTCCCCCTTGAT | 79658 |
| rs549010647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147834423 | GCAGAGAGCTATTAT[C/T]GTGCCACTGCACTCT | 79658 |
| rs549028636 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147918384 | TCGTGATCCACCTGC[C/G]TCGGCCTCCCAAAGT | 79658 |
| rs549044009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147892904 | AGAGGGTAGAGGGCA[A/G]CTGTGCTGCTGAACA | 79658 |
| rs549045399 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147900004 | ACTCTGTTTACAATA[A/G]TGTCTCCTTAGACTT | 79658 |
| rs549056492 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148052677 | AGTGCCTTCTTGTGG[A/T]AGGATGTGGTCTCTG | 79658 |
| rs549070492 | in-del | -/T/TTTTT/TTTTTTTTTTTTTTTT/TTTTTTTTTTTTTTTTT | 0.375399 | 0.216275 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147837643 | AATCTCTGGTCACTG[lengthTooLong]TTTTTTTTTTTTTTT | 79658 |
| rs549071599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148038293 | GGAGATTTTATTGTC[A/G]TAGTATTTGCCATGT | 79658 |
| rs549078771 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147759426 | AAAAATTAAAAAACA[A/G]GTGAAGGTGTAATGG | 79658 |
| rs549091984 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147948790 | TGAAACCCCGTCTCT[A/G]CTAAAAAATACAAGA | 79658 |
| rs549101822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147733179 | TAGGCTTGGTGCCTT[C/T]CTCCCCTGAACTTCT | 79658 |
| rs549126489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147774750 | CTTGCTTAAAGAGGT[A/G]AGCAAGATTACCTCT | 79658 |
| rs549134191 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147835963 | CAGCATCTGCTGCAT[A/G]TCCTTATTAGGCAGA | 79658 |
| rs549145340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147946386 | TCCTTACTCCCAACC[C/T]ATCTCTTATTTTTTG | 79658 |
| rs549146098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147862227 | GTGTGCATGCATACC[C/T]GGCTGGGTGGCAACA | 79658 |
| rs549157101 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147994740 | TGTCTTTCTCTGCCC[C/G]AGCAATACGTAAAAG | 79658 |
| rs549165212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147819681 | CTCCTGCCTCAGCCT[C/T]CTGAGTAGCTGGGAC | 79658 |
| rs549169755 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148021289 | CCTTTCCCCAACACC[C/G]TCACTTCAAACTGGA | 79658 |
| rs549182273 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147953237 | CTTCTCATAATGCCT[G/T]TCTCATAATGTCTTT | 79658 |
| rs549184778 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147861863 | CTGATTGGCCCATGC[A/G]CAGCCATGAGTGGGC | 79658 |
| rs549199824 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147841106 | GTAGTTGGAACTGCA[A/G]CTGCATGGCTGCAAA | 79658 |
| rs549204747 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147905828 | TTACCTTGGGCAGTA[C/T]GGCCATTTTCACGAT | 79658 |
| rs549223545 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147842650 | TTGCCTGGAGAACAC[C/T]GTCCCTCTGTTTCAG | 79658 |
| rs549234925 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148056520 | ATACTACAGAGCTTC[C/T]GTAGACCCTTCACTT | 79658 |
| rs549235342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148003958 | AATTATGCTAAGAGA[C/T]GTGAGAGAAATCTCC | 79658 |
| rs549244650 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147842870 | GGAGAAAATCCCACA[A/G]TAAGGCAGATGATAA | 79658 |
| rs549249675 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148050573 | AGAGACGGGGTTTCA[C/G]TGCGTTAGCCAGGAT | 79658 |
| rs549262122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147827256 | GCTTACTAAAACATA[A/G]CTGATGCATTGCAGA | 79658 |
| rs549263262 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147808846 | TTCTGTTCTGCTCTC[C/T]ATTTGTGTCTCCTTC | 79658 |
| rs549267612 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147918727 | ATTTAATTCACTATC[A/C]CTGGGAGTAGCCCAA | 79658 |
| rs549268994 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147785489 | GCAAAGATAATGTTT[A/G]TGATACCATAAGTCC | 79658 |
| rs549270430 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147999264 | TCTATCACCTGAGAG[C/T]ACAGCAGGAGGGACA | 79658 |
| rs549295974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147966843 | AACCATGAAAAGGTA[A/G]AATTTTTTTTTTCTT | 79658 |
| rs549309912 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147842199 | CTCGGCCTCCAAAAG[C/T]GCTAGGGTTATGGGG | 79658 |
| rs549345257 | snp | A/G | 1.64849e-05 | 0.00287092 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147881839 | ATGATTATTTGCAGG[A/G]GGACGGAGAGGTGTT | 79658 |
| rs549345674 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147856799 | GAAGATCTTTCCCAA[C/G]ATGTTTTTTTTCCAA | 79658 |
| rs549355620 | in-del | -/T | 0.0788843 | 0.182262 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147877820 | TCTTATTCTTCATAC[-/T]TTTTTTTTTTTTTTG | 79658 |
| rs549363488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147782022 | GCTGAATAGTTTTAC[C/T]GCTTAGTATGTCTCT | 79658 |
| rs549363908 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148016984 | AACCTCATCTCTATT[A/T]AAAAAAAAAAAAAAA | 79658 |
| rs549415270 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147954804 | ATTTTTAAAGTTGTC[A/C]TCAATTTTATTTCAT | 79658 |
| rs549415957 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147993481 | TATTAATTTATTCAG[C/T]AAACATTAAGCTGCT | 79658 |
| rs549419782 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147883179 | GCACTACTGTGAAAA[C/G]GACAAGTGGTTAAAT | 79658 |
| rs549429742 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148000180 | AACATGTGGTGGTTG[G/T]TTTTTTTTGTCCTTG | 79658 |
| rs549471787 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147829414 | GGCTGGTCTCAAACT[C/G]CTGACCTCGGGTGAT | 79658 |
| rs549472220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148005783 | CTTCGATGACAAAAA[C/T]GTGAAGCAGTGAGAG | 79658 |
| rs549473384 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147743073 | CAGTCTCACTCTGTC[A/G]CCCAGGCTGCAGTGC | 79658 |
| rs549473782 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147830720 | AGACGGGGTTTCACC[A/T]TGTTGGCCAGGCTGG | 79658 |
| rs549482940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148037745 | GATGCTGAGGTACGA[A/G]AATCGCTTGAACCCA | 79658 |
| rs549517789 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147828860 | AATACACATGCCTCA[A/C]CCTTTAAAAAGTCAA | 79658 |
| rs549519374 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147912249 | AGTGCTCTAAATATA[A/T]GAAATTCCTTCCAGG | 79658 |
| rs549524271 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147982854 | TGTTTTACATAATCT[C/T]GTATTTCTCAAATAC | 79658 |
| rs549525004 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147856706 | AAAATTCAAAAATAT[C/T]CAAAAATCTCTACCA | 79658 |
| rs549549486 | in-del | -/TA | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148049128 | GTCCAGATTTGTCAT[-/TA]TATGTTAGGAAGTTT | 79658 |
| rs549556890 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147888513 | TAATATGTAAATCTT[A/T]ATTTTTTCTTAAAAG | 79658 |
| rs549561033 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147926423 | GCTGGATATTGGAAG[C/T]CAGGGAGAGAGGAAA | 79658 |
| rs549565501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148011777 | CATTTTCTCTTTGGA[A/G]TTAACTGTAATCTAT | 79658 |
| rs549588640 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148010107 | TCCATTCCCCTCCAC[G/T]TTTTTTTTGTCATGA | 79658 |
| rs549588780 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147788147 | TTGATTTTTTTTTTT[A/T]AAAAAGCGTTTCTGA | 79658 |
| rs549588917 | snp | G/T | 1.65408e-05 | 0.00287578 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147875083 | GAACAAAATCAGACA[G/T]AATCCCAAGGACCAC | 79658 |
| rs549591205 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148058989 | GAAATGCCTCCGTGG[C/T]GTCAGGAACAGTCAG | 79658 |
| rs549593692 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147887995 | GTTGCTGTGCCTGGT[C/G]GTCGATTCCCAGTGC | 79658 |
| rs549596909 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147995826 | GGTTCACGCCATTCT[C/T]CTGCCTCAGCCTCCC | 79658 |
| rs549597596 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147953419 | TTCTTACTGGCAAGA[C/T]TTTTAACCACAAATT | 79658 |
| rs549598916 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147794359 | TTTGCAACATAATGT[G/T]AATTCTCACAACATT | 79658 |
| rs549603927 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148050586 | CACTGCGTTAGCCAG[C/G]ATGGTCTCGATCTCC | 79658 |
| rs549606629 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147975223 | TTGGTGTGACAGTGG[A/T]GGCCATTGTGGTGGT | 79658 |
| rs549623932 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147881288 | AAAAAAAAAAGTAAC[A/G]TTGGTATTGTCTGGC | 79658 |
| rs549633743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148005312 | ATATAAGCTAGGTGT[A/G]CTGGCTCATGGCTGA | 79658 |
| rs549642525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147973000 | TCTCAAGTGATCCAC[C/T]GGCCTTGGTTTCCTA | 79658 |
| rs549642905 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147762157 | GGACCATAGGCATGC[A/G]CCACCATGCCCAGCT | 79658 |
| rs549643309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147969080 | GAAATAATGAATTCA[A/G]TACATTTTGAGGGGG | 79658 |
| rs549650908 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147988346 | ACTTCCACTAATTTC[A/G]TTTACTAGATCATGT | 79658 |
| rs549651808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148009586 | GTACAGAATTTTGAT[A/G]TTTCCCAGTCTGGAA | 79658 |
| rs549670300 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147887206 | CAAGAGCTGTTTCCC[A/G]CTCTAGACACCCACC | 79658 |
| rs549673870 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148066601 | ATATGTACACACATG[G/T]GCACACAAATACCAG | 79658 |
| rs549677873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147754751 | TAAATGATTTTGCTA[C/T]ATAAGTTGTACATTC | 79658 |
| rs549698261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147795067 | TAAGGTAGCAGCTGC[C/T]GGTCAAGGGTGGCCT | 79658 |
| rs549708172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147761315 | AGCCACTGCACCCGG[C/T]GTAATCTCTATATAG | 79658 |
| rs549723212 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147850546 | AACAGTCACTGCAAA[G/T]GTCTGCGGCTTCACT | 79658 |
| rs549725788 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147937074 | TGAAACCATCCCCCC[C/T]ACCCCAATCGGTGGA | 79658 |
| rs549728643 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147793538 | TCTCCCCGCATAGCT[A/G]TTTAGCCAAAAATAC | 79658 |
| rs549738633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147930064 | CTGTTGTCAACACAC[A/G]TGAGTGCAAATAAAT | 79658 |
| rs549740430 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148012471 | TGGCACCAGTATGTG[G/T]GACCTCCACATAGAC | 79658 |
| rs549746689 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147877301 | CACAGTACAAATGCT[C/G]GTTCTTTAAAACACA | 79658 |
| rs549747692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148054773 | GACCCAACCACATTT[A/G]TAACTTATTCTGAGC | 79658 |
| rs549748087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147801923 | ACAGAAAATGGAGCC[A/G]GAGTTGAACTCATCC | 79658 |
| rs549771963 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147937084 | CCCCCCACCCCAATC[A/G]GTGGAAAAATTGTCT | 79658 |
| rs549796161 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147956160 | TTCTACTAGCTAAAA[A/C]CTGCAGTATTGGTTT | 79658 |
| rs549799678 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147963369 | CCCTTCCTGAGCTTC[C/T]CTGGCCAGCCCTAAG | 79658 |
| rs549802656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147803811 | ATATCTATCTATAGA[C/T]CATGTTTTCTTTATC | 79658 |
| rs549807696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147748987 | GCTGATGTCCTATAC[A/G]TAAGATAACTTTTAC | 79658 |
| rs549811601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147901588 | GGCTCAAGTTTGAGT[C/T]GTTGTGCTTGGAGGC | 79658 |
| rs549815241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147810723 | CTTAGGGTATGGTGA[A/G]GGCAGTAGTCCAGAT | 79658 |
| rs549822274 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147795641 | ATGTGAGGTGACTGG[A/T]TGAGGAGCTGCTGGA | 79658 |
| rs549822785 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147742606 | CTCCTGCCCCAGCAT[A/C]CCGAGTAGCTGGGAT | 79658 |
| rs549836202 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147936580 | ATGATCCACCCGCCT[C/T]GGCCTCCCAAAGTGC | 79658 |
| rs549846762 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147831594 | CATTTCTCAGTTTGG[C/T]TTAAAAGTTGTCAGT | 79658 |
| rs549856144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147857492 | AATTTGAGCTTCCCA[A/G]TGGATTAACCATGTG | 79658 |
| rs549861505 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147741804 | CACGCACACACACAC[A/G]CACACACACACACAC | 79658 |
| rs549874872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147749998 | TGCTTTTTGGCAGTG[C/T]TTACCTGAGTGTGGC | 79658 |
| rs549876569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147810044 | TATGTCACATATAGT[A/G]TCTCTTTATAGAGAT | 79658 |
| rs549877956 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147837319 | AAGCATTTTGTCAAG[A/T]TTGTTTATACGGTTC | 79658 |
| rs549887534 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147844111 | ACATGAGCCCTTAGT[G/T]TGTGCTCCCAGCTGC | 79658 |
| rs549900218 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147797719 | CCTGGCCAGCCAACA[C/T]GCCCGGCCCCCTCCC | 79658 |
| rs549907249 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148014452 | ATATGTTCACACCGT[C/G]AACATAACAGTGATG | 79658 |
| rs549909021 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147936392 | GGACTGCAGTGGCGC[A/C]ATCTCGGCTCACTGC | 79658 |
| rs549919903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147845093 | ATGCTCAAACTCCTC[A/G]CCTTCATCCTTTGCC | 79658 |
| rs549922544 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147802465 | CCAGCAATGTACTGA[C/G]TGTTTACTGGCTCAG | 79658 |
| rs549925769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148013556 | AGCCGGGCATGGTGG[C/T]GGGCGCCTGTAGTCC | 79658 |
| rs549927387 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148033299 | AGTCAGATGATGCAG[A/G]TGTCTTACTCATCAC | 79658 |
| rs549955290 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147843604 | CGATCTCAGCTCACC[A/G]CAACCTCTGCCTCCT | 79658 |
| rs549956306 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147796611 | CTTAACTGCAAGCTC[C/T]GCCTCCCAGGTTCAA | 79658 |
| rs549964173 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147904004 | GATTGCTGTGTCCTA[C/T]AGTAAAAATGTTTTT | 79658 |
| rs549964260 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148033836 | CTCTCACTGCTTAGT[G/T]TTTTCCTGTTAGACT | 79658 |
| rs549970683 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147931205 | GATTTTACCTTATCC[A/G]TTTTGCCCAGAGACA | 79658 |
| rs549971780 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147935550 | TAATACTTGTTGATC[A/T]GAAATAGTGATCCCT | 79658 |
| rs549974893 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889396 | CCTCTGCCTCCCAGG[C/T]TTGAGTGATTCTTCT | 79658 |
| rs549982087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148025110 | TAAGTGATTATTAAT[A/G]GTAAGAAGTTTCTGT | 79658 |
| rs550002569 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147903030 | CCTATGATCAAGTCA[C/T]CTCCCACCAGGCCCC | 79658 |
| rs550009603 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148067899 | GGACTTAAGTTATGA[A/G]TTCCAGTTCTAGGCG | 79658 |
| rs550011620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147896410 | AGATTTTCTATTTTT[C/T]TTGGGTTTTGATAAA | 79658 |
| rs550017489 | snp | A/C/G | 0.00557861 | 0.0525638 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147938107 | TTAGCAAAGTAATGC[A/C/G]GGAATAGAAAACCAA | 79658 |
| rs550037031 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147800998 | TTTAGTAGAGACAGC[A/G]TTTCGCCATGTTGGC | 79658 |
| rs550037759 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148072209 | GGGAGTTACCATCAT[C/T]ACAGTCAGCCCTGGG | 79658 |
| rs550038170 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147958543 | GAAGCAAGACAAAAA[C/T]CATGTGATTCTTGCT | 79658 |
| rs550039383 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147880809 | TAATCTAGGGTTATC[A/G]GTGTACTTTTAGGCT | 79658 |
| rs550045571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147909061 | TCACAAGTCTGGACC[C/T]TCCCATACTTCTGGC | 79658 |
| rs550050261 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148066256 | TGAGAAAACTTTTCC[A/G]GGAATTTCTTCCTAG | 79658 |
| rs550050962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147808625 | GAAGTGAGCAGATCC[A/G]TGGGATGTTTGCATG | 79658 |
| rs550063397 | in-del | -/AAAA | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147755083 | GTGAAACTCCGTCTC[-/AAAA]AAAAAAAAAAATTCT | 79658 |
| rs550084187 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147908622 | TTCTTAAAGGTTGCC[G/T]AGAATTATCACCGTG | 79658 |
| rs550088277 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147782696 | GTACTGACTGTGGTA[C/G]AACTTGTTCTGAGGG | 79658 |
| rs550089593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147943403 | AAAAAAGTGAACTAA[C/T]GTAGCTGAAAAGTAT | 79658 |
| rs550099108 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147845603 | CTGTGAACTTGAGCA[G/T]TTGTTAGCTTCTGTG | 79658 |
| rs550133989 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147797205 | CCTCAAAGTTATTCA[A/T]TTTTTTTTTTCTTTT | 79658 |
| rs550142555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148032366 | TGTAGGCCAAACGTT[A/G]TAATCATTGAGAATT | 79658 |
| rs550142664 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148024536 | GACTCGGAATGCCTC[A/C]TGTAATGACACAGGG | 79658 |
| rs550162002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147860940 | ACAACTTGGACGTCC[A/G]TGGCATTCTTGTAAG | 79658 |
| rs550167200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147756606 | ATGTGCCATCCTGCT[C/T]CATCCCACCTGGGAT | 79658 |
| rs550180998 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148033539 | TTGGTGATTTTCTTT[A/G]TACATATTTGTATTT | 79658 |
| rs550191643 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147988202 | AGTTTTAGGTAGAAA[A/C]TGGCTCTTTGAAGCC | 79658 |
| rs550196133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148047355 | ACCCAAGATGTTTCC[C/T]CACTAGTTATGCAAA | 79658 |
| rs550212626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147823634 | TGGTGGCATGTGCCC[A/G]TGGTCCCAGCTACTC | 79658 |
| rs550234596 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147764806 | TCCCAAAGCGCTGGG[A/T]TTAGAGGCATGAGCC | 79658 |
| rs550234794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148040111 | TCCACTGGGGTCACC[C/T]AGGTGCTGGTTCAGA | 79658 |
| rs550235850 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147990384 | CTAACAGTCTTAGCT[C/T]AGGCACACTGGGGCA | 79658 |
| rs550279217 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147929548 | AGACATTTAAACATT[A/G]GTGCTTACTGAGGAC | 79658 |
| rs550294769 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147738323 | TTGGGAGGCCGAGGC[A/G]GGCGGATCACGAGGT | 79658 |
| rs550296276 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147944215 | AGTTATAAAGGATTG[C/T]ACCTTTAATCAGGGG | 79658 |
| rs550302533 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147770007 | ACAGCATAAGGACCT[A/C]TGAAAAGCAAGAAAA | 79658 |
| rs550304331 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147852804 | GCTCACTACAATCTC[C/T]GCCACCCAAGTTCAA | 79658 |
| rs550307896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147867588 | AGTTGAGAGTGGGCC[A/G]GGCACAGTGGTTCAT | 79658 |
| rs550325382 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147833002 | AACCTTCCGTTGAGA[A/C]CTGGTTAGGTCAAGG | 79658 |
| rs550331059 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147950824 | CAGCAGTTTTCTGTT[G/T]TGAGGGGACAAATGA | 79658 |
| rs550335723 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148049253 | GGATTCTGTAGGTCC[G/T]AGAAGGGTCCTGAGA | 79658 |
| rs550344785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147898192 | TGCCTTAGGCTGCAT[C/T]TCTTGTAATGCAGGT | 79658 |
| rs550344923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147763903 | GGGATTACAGGCGTA[C/T]GCCGCCATGCCTGGC | 79658 |
| rs550364024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147776477 | CACCCACCTTGGCCT[C/T]CCAAAGTGCCAGGAT | 79658 |
| rs550375921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147817264 | GTGACAACTTCATGA[C/T]GAGGGCTCAGGCTTG | 79658 |
| rs550385093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147859687 | CTTATTCAGTGTTCT[A/G]TCTTCAGTTCCTAGA | 79658 |
| rs550412242 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147991274 | TTACTGGAAGGACCC[A/G]TGAGACTCTGCATTT | 79658 |
| rs550420225 | snp | A/G | 0.000126884 | 0.00796404 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147864995 | TGGTGGATTTTTGCA[A/G]TGTAAGATAAGTATT | 79658 |
| rs550435994 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147839332 | TCATGGGAGAAAATA[G/T]GGGAGATATTCCTTT | 79658 |
| rs550437317 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147824653 | AAGGTGGCAGGATGG[A/T]GTTGAGTGCAGGCAG | 79658 |
| rs550437903 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147832414 | AGCACTTTGGGAGGC[C/T]GAGGTGGGTGGATCT | 79658 |
| rs550449819 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148046355 | CCCTCCCTGATATCC[A/G]AAGGGAAATGGAAGT | 79658 |
| rs550451044 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148034558 | GGTCTTGAGCTCCTG[A/G]CCTCAGGTGGTCCAC | 79658 |
| rs550458972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148055682 | GACAGAGCAAGACTC[C/T]GTCTCAGGGAAGCAA | 79658 |
| rs550469757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147825775 | ATGTTAATAGTGTCA[A/G]TTTTTTTTCTTAACC | 79658 |
| rs550470801 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147914826 | AAAACTAATTCCTCC[A/G]CTGACCAATAACCCA | 79658 |
| rs550479913 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148040499 | GGCGTGCACCACCAC[A/C]CCTGGCTATTTTTTG | 79658 |
| rs550480770 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147946426 | CTACTACAGATTTTA[C/T]GAAGTGCCAGAAGTG | 79658 |
| rs550497670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148056150 | ATTTACTCTCTGGCC[C/T]TTTACAGAATAAGTT | 79658 |
| rs550514390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147791610 | TGTTTTTCCTCCCTG[C/T]GGGGCATGGAGTTGC | 79658 |
| rs550527429 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147735825 | TTTAGTTTTCTTTTT[A/G]AAGTACTTTCTTTTC | 79658 |
| rs550533553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147864365 | TCCTTCTCACTTGCC[A/G]CCATCACTCCCTGAG | 79658 |
| rs550535871 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148035232 | GCTTTTTGGGCAAGC[A/G]TTATGCTTAATTTCT | 79658 |
| rs550537146 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148068073 | ACCTTTCCCTTTTCT[C/G]TGGGCCTGGGGAATC | 79658 |
| rs550546736 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147795935 | CCTGACCTCGTGATC[C/T]GCCCACCTCGGCCTC | 79658 |
| rs550556278 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147992839 | TATGAGCTTGTACCA[C/T]GGGACTTTCTACTTA | 79658 |
| rs550556784 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148004100 | CAGGTCCAGTGGTGC[A/G]CGCCTGTAATTCCAG | 79658 |
| rs550559268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147778967 | TGAACTAAGGTACTG[A/G]AAAGGAAAGTAGAAA | 79658 |
| rs550593699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148004596 | TGTGGAGAGGGCCAC[A/G]TGGCAGGAAACCGCA | 79658 |
| rs550595353 | snp | A/G | 4.94539e-05 | 0.00497238 | missense, utr-variant-5-prime, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147822908 | CAGATGCTTCCTTAC[A/G]TGAATTTTCAAATTT | 79658 |
| rs550595361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147991776 | CCTTTCTAAGGATAG[C/T]AGGCTCAGGCCTGCT | 79658 |
| rs550598219 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147970406 | GTCTGAGAAAGGAAA[A/G]CATTACAGTAATGGA | 79658 |
| rs550612045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147880389 | TAATGAAACAGACAT[A/G]GAAAATTAGTCATGG | 79658 |
| rs550617604 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148028470 | GGTAATAATAGTATC[G/T]ACCACTGAGGATGGT | 79658 |
| rs550624140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147811784 | GCAGAGTGCAATTAA[C/T]AAGAGTGAGCTCCGA | 79658 |
| rs550627808 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147868917 | TGGACCGGTACCTGT[C/T]GGCAGCCTGGGGGTT | 79658 |
| rs550633102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147964013 | CCCAAATAAGATCGT[A/G]TATTAAGCACGCCTT | 79658 |
| rs550634657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147786307 | CTCTAAATGTGTTTG[C/T]TTTGTGAATCTGGAA | 79658 |
| rs550635382 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147922547 | ACAAAAAATAGCCGG[C/G]CGTAGTGGCGGGCGC | 79658 |
| rs550636187 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147905014 | TTCATGTGTTTTTTG[G/T]CTGCATAAATGTCTT | 79658 |
| rs550643934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147818867 | AATTATTAAAAGAAA[C/T]AGAATATGGTGTGGT | 79658 |
| rs550658373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147998461 | AAACTGGTCTACACC[A/G]TAGTGAAGGAAAACT | 79658 |
| rs550658852 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147790940 | CCTCCTCATCCTGTG[C/T]CCTTACCATTCTATA | 79658 |
| rs550659897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147918205 | CAGTGGCTTGATCTC[A/G]GCTCACTGCAAGCTC | 79658 |
| rs550667128 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147752653 | GTGCCTCAGCCTCCC[A/G]AGTAGCTGGAATTAC | 79658 |
| rs550671880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147966654 | TCCTTTGGTTAAACA[A/G]ATTCCTCCCCCCTTA | 79658 |
| rs550674546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148066623 | AAATACCAGTGTCTC[C/T]GTGTGTTTTGGAGGA | 79658 |
| rs550681077 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147910927 | CCCCTGAGGCACCTT[C/G]TTACCCCTCTTCCTT | 79658 |
| rs550707572 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147960346 | TTAGTGTCCTCAGTT[G/T]TAAAATATCATTTCT | 79658 |
| rs550718141 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147739565 | GTATTTGCTATGGTA[A/G]ATTCACAATAAAAGA | 79658 |
| rs550721117 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147964482 | CTAAACTTTTCCCTT[C/T]CTGACAGTCATTTTC | 79658 |
| rs550731506 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147777667 | CACTGACTGACCTTT[A/G]AGGGTGACTCATGTC | 79658 |
| rs550744063 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147788048 | ATCATCGGTTCCTCT[C/T]CACATCTCTTTTCCT | 79658 |
| rs550754623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147745987 | TAGAGATGGGGTTTC[A/G]CCATGTTGGTCAGGC | 79658 |
| rs550755369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147886465 | CCACCTTCTTTCCTA[A/G]TAAGTACCCTTAGAT | 79658 |
| rs550770961 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147793048 | GAGGCTGAGGCAGGA[A/G]AATCACTTGAACCTG | 79658 |
| rs550772776 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148004713 | CTGCCAACAACCTGA[A/G]TGAGTTTGGAAGCAG | 79658 |
| rs550785364 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147845454 | GTTTATCTCGTAAAA[G/T]AGATAAATATTTAAA | 79658 |
| rs550786910 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148007681 | GTAACTTCAGCAATT[C/T]GGAAGGCTTTTCCCC | 79658 |
| rs550792188 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147885939 | CTTCCAAATGCAAAA[A/G]TTTTTTAGCACTGGC | 79658 |
| rs550792867 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147785444 | GTGCCCGTCAGATCA[A/C]TAGTGTGTAACTTTT | 79658 |
| rs550804955 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148013944 | GACTGCCAATTTTAC[A/G]TTTACTACTTTTTGA | 79658 |
| rs550807298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147784380 | AATACATATTAAATT[A/G]TATATAATTTATAAA | 79658 |
| rs550808902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147744474 | AAGTTTTGTGTAGGG[A/G]AGTGGTGTGAGTTGA | 79658 |
| rs550809513 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147878502 | TTTAGACTAGATGCT[G/T]CTTAGCACTATGATT | 79658 |
| rs550824654 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147761621 | GTTTTTGTTGAGTTA[A/G]CAATTATATCAGGCA | 79658 |
| rs550834648 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147841287 | GCATTTTGCGACTTC[G/T]TTTCTTGGCTGGTTC | 79658 |
| rs550844934 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147985413 | TGGGCACCCAGCAGG[G/T]ACACATGCAAACCAG | 79658 |
| rs550845175 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147758240 | TGCACTGCAGCCTGG[C/G]CAACAAGAGCGAAAC | 79658 |
| rs550845666 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147878207 | TTCAGCCTATTCACC[A/T]GCCTCAGCCTCCCGA | 79658 |
| rs550849580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148007373 | GAAGGAAGGGAGCTC[A/G]GATTCCAGCATGGTA | 79658 |
| rs550852218 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147923214 | GTGGGTAATATATTA[C/G]ACGTAGAAAAGTACA | 79658 |
| rs550865412 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148069992 | CAGTGAAGGCATGAA[G/T]GAAGTAACTTGCTGC | 79658 |
| rs550886252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147978654 | TTTCCTGAGGCCTCC[C/T]AGCCATGCTTCATGT | 79658 |
| rs550890468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147977405 | GAGCTAGTGCTCACT[A/G]TGTATTTTTTCTTTG | 79658 |
| rs550906751 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147757654 | CCTCTGAACATTGGC[A/T]TACTCACGGGCCTCT | 79658 |
| rs550908948 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148006376 | CTGACAACGAAAATG[G/T]TGGGAACGTCAAATA | 79658 |
| rs550927080 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147808651 | GCATGTAGAGTGAAT[A/G]TGTAGGGGGTTAAGG | 79658 |
| rs550957466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148017070 | TGAGGCAGGAGAATC[A/G]CCTTTTATGGAGACT | 79658 |
| rs550966350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148051040 | AACAAAAATGCTAAA[A/G]TCTTGTCCACTGGGA | 79658 |
| rs550972263 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148040969 | CTTTCTTTTGATCCT[A/T]TTAACTACTTGTTAA | 79658 |
| rs550977087 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147868015 | TGTCAACTTGTATTT[C/G]AGGATTGTTTGGACA | 79658 |
| rs550994016 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148063557 | TGGTGCTGGTTGTGC[A/G]TTTATGAAGAAGTTC | 79658 |
| rs551008581 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147801085 | TGCTGAGATAACAGG[C/T]GTGAGCCACCGTGCC | 79658 |
| rs551009560 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148008904 | GTCTACTGTTAAGTC[A/G/T]GACGTTAAAGAGATT | 79658 |
| rs551019160 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147800469 | GGTGGGGCTTTAGGT[A/T]GGTCCTTCTTTTGGA | 79658 |
| rs551036596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147765764 | ATGATTGCACAACTG[C/T]ACTCCAGCCTGGGCG | 79658 |
| rs551048505 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147972313 | TCTTTGTGTATCCAT[A/G]CACTTAAAAATATAT | 79658 |
| rs551050694 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148058132 | TACAGATCTACAATA[C/T]TTCCTTCTGTCTTTA | 79658 |
| rs551053097 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147777407 | GGGACTACAGGCACC[C/T]GCCACCATGCCTGGC | 79658 |
| rs551057017 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148066017 | GAGGGGATTAGTTTA[C/T]ACAATAGTAAGTGTG | 79658 |
| rs551063701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147900869 | GACAGGTTCTTGTTA[C/T]TTTGCCCAGGCTGGT | 79658 |
| rs551072658 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147834543 | CTTTTAAGGCCCCAC[C/G]TCTCAATAATGCCAG | 79658 |
| rs551073755 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147794424 | ATTTTTTTTATTGAA[A/G]TGTACCACATATATA | 79658 |
| rs551078174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147806968 | TTTCCAAGTCTCTAG[C/T]AAGCGTGAAACCCGG | 79658 |
| rs551087293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147965994 | GATGGTATCTTTGAA[C/T]TGAGACCTGAATTAA | 79658 |
| rs551097783 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147745633 | AGTAGCTGGGACTAC[A/C]GGCGCCCACAACCAC | 79658 |
| rs551102876 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147933665 | GACCCAAAAAAGATA[A/C/T]TGGGACTGTGTGGGA | 79658 |
| rs551129818 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148050598 | CAGGATGGTCTCGAT[A/C]TCCTGACCTCGTGAT | 79658 |
| rs551148557 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147977768 | CATATGGTGAACATA[C/G]TACTCAACAGGAAGT | 79658 |
| rs551166661 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147932588 | TGTTTTCACTTACAA[G/T]TGGGAGCTAAATAAT | 79658 |
| rs551168574 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147924122 | ATAAATCCAGGCACA[C/T]CAGGACTGAATATTC | 79658 |
| rs551171402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147987455 | CCCTCCTCAGTCTGT[A/G]GTGCCCTGTAGTCAT | 79658 |
| rs551174849 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147849958 | CAGCTGGGCTTCTGG[A/G]TCGGGTGGGGACTTG | 79658 |
| rs551202729 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147798608 | AACATGATGAAACCC[C/T]GTCTCTACTAAAAAT | 79658 |
| rs551219059 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147999327 | ATCAATGGCTACCCT[C/T]TTTGGGTACCCTCCC | 79658 |
| rs551219383 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147891233 | AAACAACCTAAATGT[C/G]TGTTAAGAGATGAAT | 79658 |
| rs551228852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147941045 | GACTCAGGTTGCCAG[C/T]GGTTCAGTAGCAGCT | 79658 |
| rs551238195 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147891720 | ACTATCACTACATGA[C/T]GTCAGCCACATTTCA | 79658 |
| rs551249045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147805283 | AGAGATCAGATGGTT[A/G]TAGGTGTGAGGCTTT | 79658 |
| rs551258081 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147759996 | CTCAGGTGATCCACC[C/T]GCCTCAGCCTCCCAA | 79658 |
| rs551258941 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147922539 | CTAAAACTACAAAAA[A/T]TAGCCGGGCGTAGTG | 79658 |
| rs551265249 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147885947 | TGCAAAAATTTTTTA[C/G]CACTGGCATAATGCC | 79658 |
| rs551273667 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148037479 | GATACTTTGACCTGT[A/G]TGTACCACATTTGAG | 79658 |
| rs551298862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147938666 | TTCATCACTCCGAGC[A/G]GGGAGGTGAAAAGAA | 79658 |
| rs551308421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148030673 | AGCTGTTGAGGAAAA[A/G]GAAATGATGCAAGAC | 79658 |
| rs551312432 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147812538 | TCTCCGTTTCCTTCC[A/T]GTCTTCCTGGGAACT | 79658 |
| rs551315387 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148059462 | CAACAAGAAAAAAAG[G/T]CAATAAATAGATTTT | 79658 |
| rs551318659 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147814149 | CACCCTCTTTGTATT[A/C]GTACAGCACCATGGG | 79658 |
| rs551327866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147858586 | TGGATGGCACTTGAC[A/G]GTTCATAAAAGAGAA | 79658 |
| rs551337596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147746642 | TGATCCGCCCACCTC[A/G]GCTTCCCAAAGTGCT | 79658 |
| rs551347082 | in-del | -/G | 0.0130921 | 0.0798413 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147988170 | AAACAGATGGAGCGT[-/G]TGTGTCTGGTCAACA | 79658 |
| rs551361725 | in-del | -/ATT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147865477 | TGATTTTTGTTTGTG[-/ATT]ATATAGATGTTTTCT | 79658 |
| rs551378076 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147820883 | GGCGTGAACCACCAC[A/G]CTGGCCATATTTTAC | 79658 |
| rs551379000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147949358 | GCATCTTTTAAGTCT[C/T]GTTCACTGCAGTATC | 79658 |
| rs551383996 | snp | C/G | 1.64904e-05 | 0.00287139 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147881953 | TTATTGGAATTATTG[C/G]ACATGGTGAAAGAGT | 79658 |
| rs551387866 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147997238 | GTGGAATCTACAAAC[A/G]TATTGCAGCAGGAGG | 79658 |
| rs551388539 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148059287 | AGCTTTTTAGGAACA[A/G]TTGACTTCTTCCTCC | 79658 |
| rs551388719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148010192 | TGATTAAATGGTATA[C/T]CTGTGTTAATAACAT | 79658 |
| rs551389635 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | ARHGAP10 | GRCh38.p7 | 4:148072951 | GCGTGTTCCTGGGGG[C/T]AGCAGCAGCCTCTGA | 79658 |
| rs551392446 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147760298 | GAAGGAGGTAAGTGC[A/G]TCGGGTTACAATATC | 79658 |
| rs551403261 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147814291 | TTGCTAGGATGCATC[-/T]TTTTTTTTTTTTTCC | 79658 |
| rs551405635 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147740627 | TAGACATTCCAAGGT[C/T]GGGTTGATTTAGTAT | 79658 |
| rs551410905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911597 | TTGATCTCCTGACTT[C/T]GTGATCCGCCCACCT | 79658 |
| rs551421486 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147943417 | ACGTAGCTGAAAAGT[A/G]TAAAACATATTTTCA | 79658 |
| rs551425168 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889621 | TTGGATACCTTCTTA[C/T]AGCAATTTCTCAGTT | 79658 |
| rs551430038 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147817989 | AGGACCTGGGAATAA[C/T]GTGAAATCTCTTGAA | 79658 |
| rs551453169 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147756424 | TGTTTCTCCATTAAC[G/T]TCAGTTAATCAGCAG | 79658 |
| rs551460512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148065004 | GTGAGTCTCCAGATT[C/T]GGGTATTGACTTTGC | 79658 |
| rs551465963 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147837849 | CAAGTGCTGGGCAGC[C/G]CAAAAGGACTGATGT | 79658 |
| rs551483133 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147972184 | AAGTATAACGTAAGG[C/T]ATAGTTAAAGACATG | 79658 |
| rs551483559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147753497 | TATAGGTGTGCACCA[C/T]CGTACCTGGCTAATT | 79658 |
| rs551489937 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147734701 | CAACTTCCCCTGTCT[A/G]CCTCTTAGGGGAACT | 79658 |
| rs551493406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148071342 | AGTTTGAGGCTGGGA[A/G]TGGTGGCTCACGCCT | 79658 |
| rs551503342 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147849120 | CCTTTTTCCTGGTAG[G/T]TTTGTGTACCATAAT | 79658 |
| rs551526563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147856567 | ATGTACAAAATTATT[A/G]AAAATATTGTATAAA | 79658 |
| rs551529586 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147989210 | AGTATACGAATAGGT[A/G]TGGGTGACAGACATC | 79658 |
| rs551536220 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148030121 | TGTGGAGGAGGAAAA[A/C]AAAAAAGCTTATTTA | 79658 |
| rs551544854 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147760350 | CAGATGACTATGTCA[A/G]TATCTAGAGAGCTTA | 79658 |
| rs551555940 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148045848 | TTCTAGGACCTGGGA[A/G]TGAGGAAACGTGAAG | 79658 |
| rs551565192 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147845720 | ACTAGTTGGGTAGAT[C/T]CAGATGTGGGAGCTT | 79658 |
| rs551572315 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147766631 | GTATACACATATATA[G/T]ACGTATATACACACC | 79658 |
| rs551575874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147734025 | GGCGCCTATACATAT[A/G]GAGGAGTGAGCATAG | 79658 |
| rs551577210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147815750 | TCATGCCTGTAGTCC[C/T]AGCTACTCAAGAGGT | 79658 |
| rs551587744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147822576 | GCCAGGTTGAAGATG[A/G]CGGGCCATTTGGCAA | 79658 |
| rs551590264 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147752271 | TATCTTGTGTAAAGT[C/T]GTGGGGTTGTAATGT | 79658 |
| rs551592707 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148070393 | TTACTGAATGTAAGG[A/G]AAGTGCAGGCGGTTA | 79658 |
| rs551598149 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147986984 | TTCATTGTGACTGTT[A/T]AATAGGCTACACTGA | 79658 |
| rs551621857 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147747563 | TTCAGGGATGTGGAG[C/T]GTGGAGACCTTCAGA | 79658 |
| rs551633812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147913352 | TATATGAAAACATGA[A/G]GTCAGTGTTGAAATG | 79658 |
| rs551646492 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147813489 | TTAGGAAATCAGAAG[G/T]AAAAAGCCGTGGGAG | 79658 |
| rs551647361 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147835177 | TGAGGAAACCCTTGT[C/T]CAGAGTGCTCAGCTA | 79658 |
| rs551660065 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147870829 | GGATTTGTAAAGAGT[A/C]CCTAGAAGATAACAA | 79658 |
| rs551663719 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147993099 | AGCAGGGTTTGGCTT[G/T]TGCTTTTGTTTATAT | 79658 |
| rs551667038 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148012625 | TCCTAATGTGTTTAG[A/T]AATTGAATCTTGCCT | 79658 |
| rs551669194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147836051 | TACTTAAAAACAAAT[C/T]TTTACAGGTAGATTG | 79658 |
| rs551685622 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147927509 | TGGAGTATATCACAC[A/T]CTCTCACACAGTCTC | 79658 |
| rs551702138 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147765893 | TTTTGGAGATACACA[A/G]TGCTGTGATTACAGT | 79658 |
| rs551705821 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147828660 | CTGGTTTCCTCCTTG[A/G]GGGGAAACTGTTGAA | 79658 |
| rs551709930 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147769221 | AATTACTCAGTAAAT[A/G]TTGAAGAAGAAGGAA | 79658 |
| rs551734666 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147732111 | GCAGCTAGCGCTGGT[C/T]TCGGTGGCAGCTCCT | 79658 |
| rs551742554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147740906 | AAGGGGTAGGACCTA[C/T]CTCAGATCTGGTGTT | 79658 |
| rs551751512 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147776646 | TCTAGAACTTTTGAT[A/C]AATGTGCACAAGAGA | 79658 |
| rs551756784 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148010836 | AATGTTTGAGATGTA[C/G]TGCTCTAATGGTAGT | 79658 |
| rs551756901 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147788252 | GAGTTTGAGACCAGC[A/C]TGACCAACATGGTGA | 79658 |
| rs551760962 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147951405 | TGTGGTATAGTTGAT[-/T]TTTTTTTTTTTTTCA | 79658 |
| rs551762090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147782998 | ATAAATTATATATAT[C/T]ATATAAATTATATAC | 79658 |
| rs551781060 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147816278 | TCCAGTCCCCACATC[A/C]CTCCTGAAGGATTCT | 79658 |
| rs551798500 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148002063 | GTTTATCAGAAATAG[A/C]TCTTATTATTTTGAG | 79658 |
| rs551810354 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147906898 | AAGCAGCAGTACATA[A/T]AAGACTAGTGTATCA | 79658 |
| rs551810820 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148013016 | ATTATCACCTTTGTA[A/C]CATGAATAAATTGTA | 79658 |
| rs551810876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147877351 | CAGGTCTTTGGACTG[A/G]TGATGGTCTGAGATA | 79658 |
| rs551813436 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148041615 | AATTATCAAGCTCTT[A/G]TTTCCTCCTCTTGGT | 79658 |
| rs551818469 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148025166 | GGAACACTCAAGCTA[G/T]TGTACAATCACAGCC | 79658 |
| rs551821373 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147919389 | CTCATGATGTTTTGG[C/T]ATGTGTGGGAGTCAC | 79658 |
| rs551830393 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147747244 | GATGTCTACAGGGAA[A/T]AAAATGCCTCTGGCA | 79658 |
| rs551838477 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147909194 | TTATAAAAGTTACAA[C/T]TCTGCAAGGGCCCAG | 79658 |
| rs551853640 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147969837 | GGTTTTCCTTCTCTT[A/C]CTTTCTGTGGCTAGA | 79658 |
| rs551860227 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147949147 | CTTTGTGTAAAGAAG[A/T]TGTTTTCAGCCACTG | 79658 |
| rs551861904 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148001477 | TAGCTTGATGGGGAT[C/G]GCATTGAATCTATAA | 79658 |
| rs551862849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147988370 | ATCATGTTTTCTGAG[A/G]TCTTAGTCTCTATTC | 79658 |
| rs551863956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147749859 | GTTGTGGCTTAATTG[A/G]TACTGTCTAAAAGGC | 79658 |
| rs551866648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147865304 | ATGGGTTGTTTATAC[C/T]GGTTCAAACTTTGGT | 79658 |
| rs551876328 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148000882 | TCTTTAGGTTGCCTG[A/T]TCACTCTGATGGTAG | 79658 |
| rs551879117 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147783794 | AACACACATTAAATT[A/G]TGTATTATATTTATA | 79658 |
| rs551880612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147901628 | AATACTACTTTACTT[C/T]TTACGCTTCTTTGGA | 79658 |
| rs551907706 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147878182 | CTCACTGCAACCTCT[C/G]CCTCCTGGGTTCAGC | 79658 |
| rs551911870 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147956929 | GAAGAGGTTCCTAAG[A/C]GGTAGGAGCTTATAT | 79658 |
| rs551912356 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147861659 | TTCTGCAGGCAGGTC[A/G]ACGTAATGAGTGTCC | 79658 |
| rs551912808 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147976157 | ATTGAGTGAGTAATA[A/T]CCAAACCATTTTCCA | 79658 |
| rs551932948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147749146 | GATTAATTTTAACCA[C/T]AATAGAGGAGGTGAG | 79658 |
| rs551935826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147775503 | GGGGCCTATCAAGCC[C/T]TGCTCTCACATATGC | 79658 |
| rs551945401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147876937 | GGTCATACAACTACT[A/G]AATGCTGGAGTTGTC | 79658 |
| rs551952204 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147909656 | TATTTTTTTTTGTAT[A/G]GTCCTCAGTGTGCCT | 79658 |
| rs551959055 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147934289 | AAGCTTGTGGCACAT[C/T]AGCCACCTGGATGTT | 79658 |
| rs551963177 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148038424 | ATTTTATAATCCCCC[C/G]CATTTCAGGTTCTTC | 79658 |
| rs551969358 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147870352 | AGGCGTGAGCCACCG[C/T]GCCCGGCCGCATATA | 79658 |
| rs551969362 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147741667 | TTTTGTATTGAGAAG[G/T]CCTTGATATTGTTCT | 79658 |
| rs551980164 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147883238 | GAAAGAGAATGTCAG[G/T]GAAAAAGAGGTTGGG | 79658 |
| rs552003209 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147774899 | CCACAGCCCTTTCCT[C/T]CTTGATGTATTTTTT | 79658 |
| rs552010744 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147744376 | GATAAGAATGGTGCT[A/G]TCGAGGGGGTGGGGG | 79658 |
| rs552020228 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148005361 | GCTTGAGGCAGGAGG[A/G]CCACTTGAGCCCAGG | 79658 |
| rs552021545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147876374 | GAGGTGGGCAGATCA[C/T]GAGGTCAGGAGATCG | 79658 |
| rs552021864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147963226 | AGAGCTGTCTCTGCA[C/T]AGGCTCTGTGCTTTT | 79658 |
| rs552035527 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147755431 | GGGAGGCTGAGGCAG[G/T]AGAATCGCTTGAACT | 79658 |
| rs552035851 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148000462 | GGGATGGCTGGGTCA[A/T]ATGGTATTTCTAGTT | 79658 |
| rs552040672 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147912436 | ATGGCAGCTACCTGG[C/G]AGGCTGAGGTGGAAG | 79658 |
| rs552045860 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148053253 | AATTGAAATTGTGCA[C/G]TTGCATATGGGGACA | 79658 |
| rs552052916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148061832 | AGTTAAAGATCTTCC[C/T]GTGGAGGCAAGAGAA | 79658 |
| rs552054145 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147882441 | GCACTCCAGCCTGGG[C/T]GACAGAGTGAGACTC | 79658 |
| rs552060186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147875894 | CTTAACGTTTACTAC[A/G]TCAACTGTACAACCC | 79658 |
| rs552061045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147837404 | CTAGCTAGTTTGAAC[A/G]TAAAGGAAATTCATT | 79658 |
| rs552076795 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147970781 | TCCATATGTTTTAGC[C/T]TTATTTACACATAAT | 79658 |
| rs552086439 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147961378 | CTTTTGCCCTTTTGT[C/G]TGTTGGATTGTCTCT | 79658 |
| rs552098386 | snp | G/T | | | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147780823 | TAAAGGAGTGCTGCC[G/T]GCATGGCATCCTCTG | 79658 |
| rs552100049 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147754779 | TTCTTCTGTTAGAAT[A/T]ATAATGAAGTCCCTG | 79658 |
| rs552101997 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147851032 | GAAAATATGGGTTTG[G/T]GCAAGCAGCAGCACA | 79658 |
| rs552102620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147915412 | TGAGTTTCTTAAGTA[A/G]AACTTTGTGTCATTT | 79658 |
| rs552115898 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147891826 | CTCCATGGCAAGTTG[C/T]AGTCTGTCAGGAGGT | 79658 |
| rs552116532 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147923284 | GGAGTGTAATTACAT[A/C]ATTTCTTTGAGTAAG | 79658 |
| rs552119550 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148020789 | TAACAGAATGATTTG[C/T]GTTCCTTTGGGTATA | 79658 |
| rs552119919 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148012594 | CATTTCGGTTGGATG[A/G]TAAGATCTACCTGTG | 79658 |
| rs552120403 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147820836 | TCTCAAGTGATCTGC[C/G]CACCTTGGCCTTCCA | 79658 |
| rs552132424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147795819 | CCTGCCTCAGCCTCC[C/T]GAATAGCTGGGATTA | 79658 |
| rs552141363 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147957358 | TGCCTCTTTTAGAGA[G/T]TGTGGGAACAGATCT | 79658 |
| rs552152937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147888647 | TGCTTTTTAAAAACA[A/G]TTACAGACCCCCCGC | 79658 |
| rs552162592 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147854571 | TGGATTACGCTGTTA[C/T]ATTTATATATTTTTT | 79658 |
| rs552174596 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148048460 | ATTTTTTATGCTGAG[G/T]ATTGTGGATTTAAAT | 79658 |
| rs552181864 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147818260 | TTAGCGTAGAGCAGG[C/T]GCTCAATAAAGGTTA | 79658 |
| rs552187296 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148018474 | AATTTTAAAGTAAAC[A/G]GTTTTACTATTTCCT | 79658 |
| rs552191398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147950266 | ATTGACCCTTTTTTT[C/T]CTCTAAATTTTGGTG | 79658 |
| rs552204827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147988935 | GCCTATACCAAAAGA[C/T]GTTCTACTTAAATAA | 79658 |
| rs552205100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147743282 | TCGTGATCCACCCGC[C/T]TCAGCCTCAAAGTGC | 79658 |
| rs552210686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148021312 | AAACTGGAGGAAAGA[A/G]GTGGGGCAGTTTTCA | 79658 |
| rs552211757 | in-del | -/AGGGA | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148031582 | TTCCCTGGAGTCAAC[-/AGGGA]AGACATTGCCATTTG | 79658 |
| rs552221374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147790279 | CATAAGGTGGGCTTC[A/G]CCTTTGTGACCTCAT | 79658 |
| rs552222639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147797282 | TCCAGATGAAGATCC[A/G]ACCTCTTAGCCAGGT | 79658 |
| rs552237995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147832098 | GCCCGACATACACAC[A/G]CCCACCCACACACAC | 79658 |
| rs552250279 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148014877 | TAAACAAAATTAGAA[A/G]AACAGAAACTCTACC | 79658 |
| rs552282513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148055532 | TGTCTCTACTGAAAA[C/T]ACAAAAATTAGCCTG | 79658 |
| rs552298842 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147856484 | AAATTTGAAATGACA[C/G]TACAAGTGGAAAATT | 79658 |
| rs552299168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147831304 | TCCAAAGGATTTGAG[A/G]CTATAGCTGGTTTGT | 79658 |
| rs552302453 | in-del | -/C | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148042324 | ACTTCCCTGCTTAAT[-/C]CCTGCAATACCTTCC | 79658 |
| rs552313174 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147830783 | AATTGGTCTGCCAAA[G/T]TGTTGGGATTACAGA | 79658 |
| rs552321745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147844975 | CCTTTCCCAGAGCCC[A/G]CAAGGCCCGGCACGC | 79658 |
| rs552338397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147883886 | TTTCAGTACAGACAG[A/G]GTTTTGCTATGTTGG | 79658 |
| rs552339405 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147993533 | TAAAAAAGCATGTCA[C/T]GCTTTCTAGAAGTCC | 79658 |
| rs552340320 | snp | A/C/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147955116 | TTTGTGGCTCCCTAG[A/C/G]CTTTGATAGTGCTTG | 79658 |
| rs552354633 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147936267 | TTTCTTAGCAACTTT[C/T]TTTTCTTTTTTCCAA | 79658 |
| rs552373426 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147839025 | TAAGAACTCTTACAC[A/G]AGGCAAGTTCTTTTT | 79658 |
| rs552375340 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147794173 | AGGAAATTTACAGAG[C/T]GGTTATGGTTTTGCA | 79658 |
| rs552377040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889249 | CTTGTTGTGGAGTTT[A/G]TGGGTATTATAAATG | 79658 |
| rs552378268 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147770754 | ACTTAGCCCATCTGA[A/C/G]CTTCGGTGTTTGTTT | 79658 |
| rs552382838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147796508 | GGTTCATCTCTTTTT[C/T]TCCTTATTTCTTTTT | 79658 |
| rs552396196 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148063000 | AGTTTGGGCTGCAGC[C/T]CCGGCAGGATGCAGA | 79658 |
| rs552397217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148019621 | TGGGCATGGTGGTGC[A/G]TGCCTGTAATCCCAG | 79658 |
| rs552400329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147890009 | CAGTCACCTGAGGCA[C/T]GAGACAGCATATAGC | 79658 |
| rs552403255 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147990767 | CAGACGCCGAGGTCT[A/G]CTTGAGGGACGAGGG | 79658 |
| rs552424644 | in-del | -/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147984902 | GGAGGGCTTCAAGAT[-/G]GGGCAGGCCAGACCA | 79658 |
| rs552428488 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147829195 | AGCTGGAACTACACG[C/T]GGGTGCCACTATGTC | 79658 |
| rs552443916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147803200 | TTTTAGTAGAGATGG[A/G]GTTTCACCGTGTTGG | 79658 |
| rs552447753 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147984313 | GGAAGCAGTTTCTTT[A/C]AGCCCAAACTCTCCA | 79658 |
| rs552450781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148061088 | GCGGGTGTTTTCATG[A/G]AGGTTTCCTTTTTTT | 79658 |
| rs552459353 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148018958 | TATTAAACTGCTTAT[G/T]AGAAAGCTTGCTACC | 79658 |
| rs552468932 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147983335 | GGACTACAGGCGCCC[A/G]CCACCACGCCCAGCT | 79658 |
| rs552474876 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147903110 | CCAGAGCCAAACCAT[A/C]CCACATGGCCAGGGA | 79658 |
| rs552478248 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147811589 | ATGCAATGGCTTTTT[A/T]TAAAAAAAAAAAACA | 79658 |
| rs552482563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148026858 | GTTTGCTTTCATTTC[A/G]TTTTCAAGTTATATC | 79658 |
| rs552483176 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147777072 | GCTATGCTGATAGCT[C/G]TTACAGTCAGTTTTC | 79658 |
| rs552491415 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147762829 | GCCACCACACCTGGC[C/T]GCTTTTTTATTTTTT | 79658 |
| rs552516804 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147809371 | CATTTTTTTTCTTGA[C/T]CTTAAATTAGCTTCC | 79658 |
| rs552518129 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147839513 | TAGTAGTTATACTGA[C/G]TTACTCAGTTTTACC | 79658 |
| rs552518629 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147801965 | GGATGTCTGGGATGG[G/T]AGGCATTGATTTCTC | 79658 |
| rs552526386 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147791733 | GAGATTATAGGCACC[C/T]GCCACCATGTCCAGC | 79658 |
| rs552538208 | in-del | -/T | 0.16028 | 0.233346 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147981821 | TGCTCTTACTTGTCC[-/T]TTTTTTTTACTGTTG | 79658 |
| rs552538719 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147767549 | GAGCCTATATTAAAA[G/T]ATTATCAAGAATCGT | 79658 |
| rs552568017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147885236 | AATACCCAAGACTGG[A/G]TAATTTATAAAGAAA | 79658 |
| rs552582947 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148063769 | TGGCTTCCCCCACAC[C/T]AGTGAGGTGAGGCGT | 79658 |
| rs552595847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147878527 | ATGATTCTATAATTC[C/T]ATCATTTTGAGAGGC | 79658 |
| rs552604722 | in-del | -/ATT | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147924932 | TAATTAAGTAGTCTC[-/ATT]ATTGATTTAAGGCTC | 79658 |
| rs552611175 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147990452 | CAATTTCCAAGATAA[C/G]TAAAAGTCAGAGTGG | 79658 |
| rs552624738 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147751052 | GGTGTGATGGTGCGT[G/T]CCTATAGTCCCATCT | 79658 |
| rs552625049 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147737380 | GGTTGGTCTTGAACT[C/T]CTGGCCTCATGTGAT | 79658 |
| rs552625780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147984812 | ACTTGATCCTTGTTT[A/G]CTGGGGAAACTCTCT | 79658 |
| rs552633489 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147977608 | ATAGTAGGCTCTAAA[A/G/T]TGGAATTCCTGGAGT | 79658 |
| rs552639299 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148033919 | CGGCGTTTTGGGGAT[C/T]CCTATTACTGGAAAT | 79658 |
| rs552645501 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147978720 | TTCTTCATAAATTAC[C/G]CAGTCTCAGGTAGTT | 79658 |
| rs552671466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148069518 | TTCACCTCCAGCGTT[A/G]TAGAAAATCACCTTT | 79658 |
| rs552679842 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147846029 | CTCTTAATTCTTTCT[G/T]TTAGAGCTTTGTTGC | 79658 |
| rs552683066 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147937777 | CTGAGGTCAGAAGTT[C/G]AAGATGAGCCTGACC | 79658 |
| rs552684505 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147803872 | TTCTATGTTTTGGCT[A/G]TTGTGACTACTGCTG | 79658 |
| rs552693134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147977093 | AAGCATCTGGAGATG[C/T]GGAGCTGCAAAGAGA | 79658 |
| rs552697070 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148068723 | AGCCCAGGACGCAGC[C/T]TCCCTGTGGGTCCTG | 79658 |
| rs552717165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147757741 | TTCTTCAGTCACCTT[C/T]CTAAGAGAATCTGGT | 79658 |
| rs552718913 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148007973 | TAGCATGTCCCAGTC[A/T]ATCAGGACTGCAGTT | 79658 |
| rs552735149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148056798 | CTTTTTTCCCTTTGC[A/G]TAGCTGATTTGCTGT | 79658 |
| rs552738529 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147945291 | AACTCTCCCATCTCC[A/T]TTTTTTTTTCCTGGT | 79658 |
| rs552781256 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147818966 | GGGGAAAATGAGTGA[G/T]AGAAATGCTTATATT | 79658 |
| rs552794313 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147817950 | AGAGCCTGATGGTTT[C/T]ACACCAGTTGAGATC | 79658 |
| rs552796293 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148066364 | CCAATGAGAATCACA[C/T]GGGGTATAGGATACC | 79658 |
| rs552817659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147944317 | AGGAACTGATCAAAA[C/T]GTAATCAGTGTCAAT | 79658 |
| rs552820641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147876485 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 79658 |
| rs552827499 | snp | G/T | 0.0146672 | 0.084371 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147765341 | GTGTGTGTGTGTGGG[G/T]GGGGGGGTGTGAGTG | 79658 |
| rs552836279 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148068030 | TGTAAGGTCTCAGGG[C/T]AGTGACGTTCCTGTG | 79658 |
| rs552840462 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147815546 | GTCCTTAAAAGAGAG[A/G]AGAGATGTGATGACA | 79658 |
| rs552847319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147909642 | AGCTTATAAAAATGT[A/G]TTTTTTTTTGTATGG | 79658 |
| rs552891817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147840066 | TGATAGAGATGGATG[A/G]GGACCTCCGCTGTCC | 79658 |
| rs552912280 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147791996 | TACATGTCTCCTGAC[A/G]CGTGTATGATGTGTA | 79658 |
| rs552924158 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147825541 | TTGTGTGTATATATT[A/G]TAGATACTGTAGAGG | 79658 |
| rs552946444 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147859843 | ATGAAGAGATCCTAA[C/T]GATGAATAATTTGTT | 79658 |
| rs552963058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147820486 | AGATGGGTTTTCACT[A/G]TGTTGGCCAGTCTGG | 79658 |
| rs552963873 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147773558 | TTGTATTCTGAGTTA[C/T]AACACAGCAAACTGA | 79658 |
| rs552985034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147923516 | AAATCTTCCATATGT[A/G]GATAATTTGAATATT | 79658 |
| rs552989253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148022126 | TAAAAAATATAAAAC[A/G]GTGAGACATTCTCAC | 79658 |
| rs552991156 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148014466 | TGAACATAACAGTGA[G/T]GCAGCTTTGGCTTAA | 79658 |
| rs553004975 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147817591 | ATCTCAAATATAACC[A/C]CTCATCTCTCAAACT | 79658 |
| rs553006683 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147868786 | TCCACGTGCGCAGTT[C/T]ACAATACGGTTCATG | 79658 |
| rs553014846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147999408 | TGGTCCGTGTTTGTT[A/G]CAGCTGGAGCTGAGC | 79658 |
| rs553014894 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147992355 | CCCTCCCAGATCTGC[G/T]CCCTCTATTTGTCTT | 79658 |
| rs553044621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147798135 | CTTCAGTTTTGCTTT[C/T]ACTTTTTTTTTTTTC | 79658 |
| rs553045104 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147977804 | CACCCTTTCTCTCTC[C/T]CTCCCCCTCCCCCTC | 79658 |
| rs553056805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147797385 | TGGAGTTGTTTGTTT[C/T]TCTCATGGTCCAACG | 79658 |
| rs553060749 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148054091 | TTTTGTTGTTAAAGA[C/T]TTTCTTACTTGATGC | 79658 |
| rs553062938 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147804947 | CTCTGTTGATAGTTT[A/C]TTTTTGCTGTGCAGA | 79658 |
| rs553071391 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147757167 | AGAACCTGAAAGTTA[A/G]TGGGAACACAGGACA | 79658 |
| rs553074811 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147994947 | TTATTGATGGGTCGA[C/T]GTGGAAAGGTCCTCT | 79658 |
| rs553076379 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147772987 | GGAATTAAGTAGGAA[A/G]GATTTTGACGGAACT | 79658 |
| rs553083952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147764659 | GTGCCTCAGCCTCCC[A/G]AGTAGCTGGGGTTTA | 79658 |
| rs553083966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147813497 | TCAGAAGGAAAAAGC[C/T]GTGGGAGCCGAAATT | 79658 |
| rs553095259 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148030257 | GTGGAGTGGGTTTTT[C/T]CTCCACTTCTAATAG | 79658 |
| rs553104164 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148034681 | GATGAGAGGAATAGG[C/G]GAGGACAGGTGAAAA | 79658 |
| rs553109842 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148026360 | CCAGCATGAAGCCGG[A/G]GGGGAGATCCTCTGC | 79658 |
| rs553112311 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148001124 | ATCCAGTTTCAGCTT[C/T]CTACATATGGCTAGC | 79658 |
| rs553113266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147862026 | CACCTAGGAACCTGT[C/T]TCCCGCAGCTGTCAA | 79658 |
| rs553118977 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147750655 | AACCCAGGCTGGAGT[A/G]CAGTGGCGTGATCTC | 79658 |
| rs553126285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147804067 | TAAACTGTGTGTCAC[A/G]GGGGTTTGGTGTACA | 79658 |
| rs553134991 | in-del | -/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147982546 | CACACCCAGCTAAAT[-/C]TTTTTTTTTTTTTTT | 79658 |
| rs553141294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148027970 | ATTATACTGCATATC[A/G]ATTGAAGAGCTTTTA | 79658 |
| rs553145091 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147887731 | GCCGGGTGTGGTGGC[A/G]GGCGCTTGTAGTCCC | 79658 |
| rs553147700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147874462 | GTAGGTGAGATTTTT[C/T]TTCCCCCTTCTGTCT | 79658 |
| rs553148322 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148022714 | AAAGAGGGGTTAGAG[C/G]GTATTAAATGAATTG | 79658 |
| rs553151034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148021715 | GATGACAGTAAATCC[A/G]GCTGTGGATAATAGT | 79658 |
| rs553154166 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147953596 | TTAGAATCTGCACTG[A/T]TTCTGCAGTCACCTT | 79658 |
| rs553190159 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147866147 | AGATCACTTCTTTTT[A/T]CTTCTAGATTTATTG | 79658 |
| rs553218464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147771204 | GAAAAAAAGAATCCC[A/G]TGTCTGAATACAGTC | 79658 |
| rs553221390 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147873469 | GAGGGTTGATGAGGG[C/T]TGGAAGGAATCTCAG | 79658 |
| rs553231908 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARHGAP10 | GRCh38.p7 | 4:147731680 | ATCTCCTGCAAGGCA[A/G]CCACTTCAGAGTTAT | 79658 |
| rs553246809 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147991397 | TCCAAATCCACATCC[C/T]GGCTTCCTCATGTTT | 79658 |
| rs553247624 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147976746 | TGTGGCTCTGTAAAT[G/T]GTAGATTGTATTTTC | 79658 |
| rs553248222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148050669 | TGAGCCACCGTGCCC[A/G]GTTGATTCATCTTCT | 79658 |
| rs553256738 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147780957 | TTTGGGAGAATGAGA[A/G]AAGACGCTCCAGAGA | 79658 |
| rs553266673 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147739143 | AGTGAGCTGAGATCA[C/T]GCCATTGCACTCCAG | 79658 |
| rs553269155 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147997063 | AGAACACTGAGCAGG[C/G]AAAACTGTAGTGCAC | 79658 |
| rs553296398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148029771 | TGATTCCTTGACATG[A/G]AATTACTGTGTTGTG | 79658 |
| rs553304350 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147990756 | AAAGGGAACAACAGA[C/T]GCCGAGGTCTACTTG | 79658 |
| rs553312879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148021831 | GGTGTTGGCAGGTTA[C/T]CAGTTGGAGCAATAA | 79658 |
| rs553317820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148004171 | ATCCAGTCTGGACAA[C/T]ATAGCATGACCCTGT | 79658 |
| rs553319479 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147912724 | TATGATCATAACTCA[C/T]TGCAGCCTCTACCTG | 79658 |
| rs553325322 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147821256 | CTTTCTCTGTATTCT[A/G]TTGGCTACAAGACTA | 79658 |
| rs553335139 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148023117 | AAAAGGCTATGACCT[C/G]TTCCCTTCATTGGAA | 79658 |
| rs553347686 | in-del | -/TA | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148043788 | ATGTATATATATATG[-/TA]TATATATATATGCAT | 79658 |
| rs553356197 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147918999 | CATTTTTCCTCTTCT[A/G]CTAAATTCTCTTCTG | 79658 |
| rs553356938 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147836052 | ACTTAAAAACAAATC[G/T]TTACAGGTAGATTGT | 79658 |
| rs553361219 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147879631 | GCATGTGTCATGGTG[A/G]TTTGCTGCACCCATC | 79658 |
| rs553372616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147847313 | GCAGCTTTGAAGGAG[A/G]TGCCGGAGCAAACCA | 79658 |
| rs553382336 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147732190 | CGCGCGCCCGGGCCT[A/G]CTAGCTCCTCTGTGC | 79658 |
| rs553407912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | ARHGAP10 | GRCh38.p7 | 4:147854707 | AGCACAAAGAAACAA[C/T]AATACTCTATAATGA | 79658 |
| rs553413636 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148010337 | AATGAACATTATGAT[A/C]TTGTGTCCTTTTATT | 79658 |
| rs553423136 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147806566 | TTATGATAAGGAGTT[C/T]GCTGCTTTCATCAAG | 79658 |
| rs553424675 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147913283 | TCAGAAGGATCAGTT[A/C]TTCATTTACTATGAC | 79658 |
| rs553428148 | snp | G/T | 3.07574e-05 | 0.00392145 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147946567 | CTAGACAAGAGGACC[G/T]TTGATGATCAAGGTT | 79658 |
| rs553431562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147813061 | GAACACAGTTCCTTA[C/T]GTTTCAGTGGCCCAT | 79658 |
| rs553455196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147961482 | TATTTAGTACTTTGT[A/G]CTAAGGTCATTTTCT | 79658 |
| rs553461985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147779069 | TTTGTGTGTATCAGT[C/T]ATCTGCTGGACTGCA | 79658 |
| rs553464245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147905565 | CGGCGTTATTTCTGA[A/G]GGCTCTGTTCTGTTC | 79658 |
| rs553466940 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147946099 | ATTTTTACCGTGGGC[A/T]TGTATAGGCAAGCCT | 79658 |
| rs553468536 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148044911 | TGAGTTTCTCCAATT[A/C]GCTAAACGTTTTTTG | 79658 |
| rs553483196 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147918376 | TCCTGACCTCGTGAT[C/T]CACCTGCCTCGGCCT | 79658 |
| rs553485972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147954942 | GCTAATATCTTAGAG[A/G]TGAAGTTTCAAAATT | 79658 |
| rs553488503 | in-del | -/GA | 0.00835141 | 0.0640778 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147921697 | AAATGTGTTTTAGGT[-/GA]ATCCCAGACAGACTC | 79658 |
| rs553489927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147780177 | TGAGCTACCCATAAA[C/T]TACTCCTTTGATGGC | 79658 |
| rs553495616 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148043752 | TATATATATGTATAT[A/G]TGTATATATATGTGT | 79658 |
| rs553495937 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148035603 | AAAATGAAACGGGAG[G/T]AGTGAGGTCGTTCTG | 79658 |
| rs553496596 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147959143 | GTATTATGTTGTAGC[G/T]ACATAGAAATGATTG | 79658 |
| rs553503873 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147820435 | GGACTACAGGCAACC[A/G]CCACCACGCCCGGCT | 79658 |
| rs553514537 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148000242 | TTCATCCATGTCCCT[A/G]CAAAGGACATGAACT | 79658 |
| rs553515984 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147827963 | GGTGTGCGCCACCAC[A/G]CCCAGCTCATTTTTG | 79658 |
| rs553518938 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148048256 | GTTCCTCAGATTACG[C/T]GGCTTTTTATAGTTA | 79658 |
| rs553521144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148003761 | TGTTTTCCATTTGTT[C/T]GGTAGATCTTCCTCC | 79658 |
| rs553524564 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147967494 | GGGTGTGGTGGATGG[G/T]GTTGACCCAGGTGAT | 79658 |
| rs553528054 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147793806 | AACAGTAAGCTTCTT[A/G]ACCTTTGTACATTGA | 79658 |
| rs553534371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148036020 | CAAACTTAGTATTCC[A/G]TAACCTATCTTTACT | 79658 |
| rs553577461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147827492 | GTTAGGAAAGGGTTT[A/G]TGGAAGAAGTATTGG | 79658 |
| rs553592346 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147881409 | TTGGGAGGCTGAGGC[A/G]GGTGGATCATCTGAG | 79658 |
| rs553600074 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147972847 | GCAATCTCTGCCTAC[A/C]GGGTCCAAGTGATTC | 79658 |
| rs553601746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147799967 | AATCTTTTGTTTTAG[C/T]AGGCAGCCACCCAGT | 79658 |
| rs553602520 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148052192 | GAGTCACTGGCAAAC[A/C]CTGTCTTCACTTCCT | 79658 |
| rs553605073 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147916214 | TAAATATGATTATCT[A/G]AAAACTAGTATTTCA | 79658 |
| rs553609307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148057578 | TTGCACAGTTGTGCC[C/T]CACATGAGCCTGGGT | 79658 |
| rs553632915 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147893221 | GAGCCACCATGCCCA[C/G]CTAATTTTTGTATTT | 79658 |
| rs553645336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148050266 | TTCTTATTTTAATGA[C/T]GTATTTATAGAAATG | 79658 |
| rs553657259 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148053862 | GCCTAATTCGTGCCT[G/T]CCTTTGCTGTGCTGT | 79658 |
| rs553670274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147792569 | TTCTCCTCACTCCGT[C/T]TCTCGGCCTCTTCCC | 79658 |
| rs553671569 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147892566 | GCTGTGGGAGTTGAG[C/G]AGCATGGGGGAGTGT | 79658 |
| rs553675933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147833379 | GCCACCATGTAAGAC[A/G]TGCCCTTCTTTCCCT | 79658 |
| rs553689773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148015832 | GAAGATCGGACATTT[C/T]ATTTCTGTCCCTCCT | 79658 |
| rs553695548 | in-del | -/GTAA | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147881514 | TGGTGGTGCATGCCT[-/GTAA]GTAATCCCAGCTACT | 79658 |
| rs553700517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147829619 | CTACTCACTTCTGCG[C/T]GTGTTCTCAGAGGAA | 79658 |
| rs553735181 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147788308 | AAAAATTAGCCAGGT[A/G]TGGTGGCATGCGCCT | 79658 |
| rs553736722 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147748564 | ACAAAATGATACAGG[A/G]AGTGGGAGGAAACTT | 79658 |
| rs553746021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147916349 | ACTCAAAAGACTACT[A/G]TGACAATACTTACTA | 79658 |
| rs553758105 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147802675 | TCCCTGTAACTTCTA[C/T]TTACACTGGTTTTTT | 79658 |
| rs553761287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147935789 | CAAGACTTGAGTGTA[C/T]GTATTTTACGTGCGA | 79658 |
| rs553765533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147843820 | CACCCGGCCTGAACC[C/T]CTTTCTTCTTTTATC | 79658 |
| rs553765835 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147954372 | CAAGTGTTTTGGGGC[A/T]CTCTTATTAGATCTG | 79658 |
| rs553778983 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147741030 | CTATACTTTTTTCCC[A/T]CTGAATATATTTGTG | 79658 |
| rs553790998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147774322 | CCCCAGGCTAGGCAA[A/G]CATGAACTCTTGTTC | 79658 |
| rs553797342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147870367 | CGCCCGGCCGCATAT[A/G]TGTATTTTAGGAAAC | 79658 |
| rs553799807 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147980208 | TTGAGGTATCTTCTT[A/T]CAATGCCTAGTTTGT | 79658 |
| rs553807170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148051587 | GCTCACTCTAGCTGG[A/G]GGTGCCGGCACCCTG | 79658 |
| rs553810737 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148066321 | AGTCACATGCTTACC[C/G]TACATCCATCATTTG | 79658 |
| rs553814886 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147836140 | CAGAATGGATGCTAG[A/C]TTTTCTTTTGTGGGA | 79658 |
| rs553820027 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147759854 | TCCAGGCTCAAGTGA[G/T]TCTCCTGCCTCAGCC | 79658 |
| rs553820436 | snp | C/T | 1.65184e-05 | 0.00287384 | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148023393 | TGGCCGTCTACAATC[C/T]TTGTCTGGAGCTGGA | 79658 |
| rs553825511 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148044364 | GTCAGGGAATAAACC[A/G]GTCCCAGACTCTCCT | 79658 |
| rs553831944 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147771245 | GGGTAAGGAATTCAA[C/G]ATGAGTACTTGAGGG | 79658 |
| rs553833075 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147878528 | TGATTCTATAATTCT[A/G]TCATTTTGAGAGGCC | 79658 |
| rs553834237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147875923 | CCAATTGCTAGTTAG[C/T]AGAAGGGATGAGAAT | 79658 |
| rs553836095 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147869995 | GTTGAAAAAAGTCCC[A/G]GTTTGTGTGTGTGTG | 79658 |
| rs553877926 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147850606 | GAAGGAAGAAACTCC[A/G]GACACATCTGAACAT | 79658 |
| rs553881175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148059735 | CCCTGCTTGCGAGCT[A/G]CCAAATTAGCCTACC | 79658 |
| rs553886943 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147902377 | TCCTTAGCATGGTGT[A/G]TTAATTCATTCTCAC | 79658 |
| rs553887080 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147927873 | TTAGATACTGGGATC[A/G]GGAGACCTCTGGGAG | 79658 |
| rs553896143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147753615 | TGCCTCAGCCTCCCA[A/G]AGTGCTGGGATTACA | 79658 |
| rs553923409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147882801 | CAGTATTACTACTTG[C/T]CTGGCATTAATTTCT | 79658 |
| rs553937429 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147850278 | AGCAGGCCGTGGACG[G/T]GGCCAAGTAAGGGAA | 79658 |
| rs553940657 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147910661 | AATGAAACATGCCCA[A/G]CTCTGTACCCTTGAT | 79658 |
| rs553942626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147925386 | AATGAAAAGGAATCT[C/T]GCAAAAAGCAACGGC | 79658 |
| rs553949905 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147904234 | TTTCTTTCTTTCTTT[A/C]TTTTATTATTATTAT | 79658 |
| rs553958819 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147746705 | GCGTGCTTCTTAATA[G/T]AGAAGGTGGGATTCA | 79658 |
| rs553967948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147948898 | GGGAACCCAGGAGGC[A/G]GAGCTTGCAGTGAGC | 79658 |
| rs553973525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148058987 | AGGAAATGCCTCCGT[A/G]GCGTCAGGAACAGTC | 79658 |
| rs553987038 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147801508 | TTAAGAGTGAATAAC[A/T]TGCTGTGTTTGTTCC | 79658 |
| rs553994364 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147806981 | AGTAAGCGTGAAACC[C/T]GGTGAAAGGATGCTA | 79658 |
| rs554002171 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147960896 | GTTGTATGAAACATT[C/G]ATTCATTTTCATTGC | 79658 |
| rs554013288 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147754277 | TTTACATAAGGCATA[C/T]GATGCCTTTTGTAAG | 79658 |
| rs554014756 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147979550 | GTGAATTTTAGAAAA[C/G]TGTTTTCTAATTCTC | 79658 |
| rs554021753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147935123 | GCCGCAGAGGATGCA[A/G]TGAACTTGGTTATTT | 79658 |
| rs554025744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147761618 | AATGTTTTTGTTGAG[C/T]TAGCAATTATATCAG | 79658 |
| rs554050622 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147745412 | CAGGGTGGTGTGGCT[A/G]TAGACCCAGATTACG | 79658 |
| rs554056379 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148010310 | TTCAAGACCACAGTG[C/T]ATTTAAATAGCAATG | 79658 |
| rs554061123 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147996857 | AGCAAAGGCCATGTT[A/G]TGAGGGAACAGGGAG | 79658 |
| rs554062838 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147775859 | GATAGAATGCTTACT[A/G]TATACCAGATATTGT | 79658 |
| rs554065989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147856174 | TTTAGGGGAGACACC[C/T]ATCTTCTCTGCATTT | 79658 |
| rs554068800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148070906 | TCTGTATTGCATTTC[C/T]GAACACTGGTGAGGA | 79658 |
| rs554073794 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148038480 | TAGTCTGCCACTGTG[A/T]CTTTTACCCAGAGGT | 79658 |
| rs554084155 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147932910 | GAAATTACTTTTAAC[A/G]TGTGAAATATGAACA | 79658 |
| rs554098347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147763988 | TCAAACTCCTGACCT[C/T]GGGTGATCTGCCTGC | 79658 |
| rs554099489 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147750836 | TCAAACTCCTGACCT[C/T]GTGATCCGCCTGCCT | 79658 |
| rs554108062 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147808173 | CAACTGTGGGACCCC[A/G]GTTACAAAGGCTGTC | 79658 |
| rs554111229 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148019028 | TAGGAAGTAATTTAT[A/T]TCCAAAATTTCAGTG | 79658 |
| rs554156492 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147940420 | GTGTTCTTTGGCATC[A/G]CAGACTAGAGGAAGC | 79658 |
| rs554160251 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148006109 | CTAACACTGGCAGCT[A/G]CCACTTCTTTCCTCC | 79658 |
| rs554163117 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147794990 | CTTTTGCAGTTGACT[A/G]TAGTCAGTTCCATAT | 79658 |
| rs554163272 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147901390 | CGTTGCAAGTGTGAA[C/G]TGTTCTGAAGAATGT | 79658 |
| rs554164472 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148069801 | CTGACTTCAGCCCTG[A/G]GCCCCTTGCCACTCA | 79658 |
| rs554178317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148053602 | TCTCCCTTCAGCTTC[A/G]GAAACGCTCTGGAAG | 79658 |
| rs554180810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147920155 | GGCACAGTGGCTCAT[A/G]CCTGTAATCCCAGCA | 79658 |
| rs554184926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148011377 | CTGGAATCATCTGGA[A/G]GCTTCTGCACTCACA | 79658 |
| rs554185155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147795928 | TCAAACTCCTGACCT[C/T]GTGATCCGCCCACCT | 79658 |
| rs554203029 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147767616 | CAGTTACTTGGGAGG[C/G]TGAGGTAGGAGGATC | 79658 |
| rs554222020 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148011955 | GCGTAAGAATAACAG[A/T]TAGTGCTGGGTTCTT | 79658 |
| rs554230732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148026384 | CCTCTGCTGGGAGAC[A/G]TGTTTTCTGTTATGT | 79658 |
| rs554235255 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147788441 | GACAGAGCAAGACTC[C/T]TTCTCAAAAAGAAAA | 79658 |
| rs554251132 | snp | A/G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148037635 | AGGTCAGGAGATTGA[A/G/T]ATCATCCTGGCCAAC | 79658 |
| rs554252396 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147888694 | TCCTCATTTCTAAAC[A/G]GAGAAACATCTATTC | 79658 |
| rs554255830 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147807492 | GAGAATTTTTCTGAA[A/G]TGGTCAGGAACGTAA | 79658 |
| rs554258384 | snp | C/G/T | 0.00199529 | 0.0315338 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147983019 | CCTAGTAGCTGGACT[C/G/T]CAGGTGTGCATGACC | 79658 |
| rs554282490 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148025296 | CATTATTTGCATGAT[A/G]TTTTGTTCTACATTT | 79658 |
| rs554305205 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148024065 | TACAAAGCCTAGAAA[A/T]CTGAGTTTTCAACAC | 79658 |
| rs554308942 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147963360 | ATTATGAGACCCTTC[A/C]TGAGCTTCCCTGGCC | 79658 |
| rs554315706 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148042509 | TCTTTCAGTTTTGAT[A/G]CTTTCTCGACCAGAG | 79658 |
| rs554325385 | in-del | -/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147763602 | GGTGTGAGCCACTGC[-/G]CCTGGCCTGGCCTGG | 79658 |
| rs554326267 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147895113 | ATTTATTTAGACTTT[C/T]CATTTATCCCAGTAA | 79658 |
| rs554328458 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147859295 | TTTTTTTTTTGAGAT[A/G]GAGTTTTGCTCTTGT | 79658 |
| rs554329753 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147934657 | GCCCAGGCAACATAG[C/T]GAGACCCGCTCTCTA | 79658 |
| rs554332647 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147870994 | AGATGGAGTCTTGCT[C/G]TGTTGCCCAGGCTGG | 79658 |
| rs554348394 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148018279 | CCAGGAAAGTTGGGA[C/G]AGCTGGGCAATCTTA | 79658 |
| rs554357014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147768825 | TTCACTGCAGCCTCC[A/G]CCTCCTGGGTTCAAG | 79658 |
| rs554360592 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147823348 | CTGGGCAATGTTAGT[C/G]CCTGACTCATACTCC | 79658 |
| rs554361303 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147819418 | AGCAAACAGCAAAAT[A/G]GAATAATGTGTATGT | 79658 |
| rs554363818 | snp | A/G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147791102 | AACAGCAAACTGTAC[A/G/T]TATTCTTTACTTTTT | 79658 |
| rs554366323 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147863800 | AACACGTTATGTTTC[A/G]ATATTATTTTACTTA | 79658 |
| rs554380322 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147871583 | GATCTTTTATTGGAA[A/T]GATAGCATTAGACAG | 79658 |
| rs554385444 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147981317 | TTTGTGGTTTACCCA[A/G]AAGTCATTCAGGAGT | 79658 |
| rs554385904 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147902606 | ATTAGCTGGGTGTAG[A/T]GGCTGTGCACCTGTA | 79658 |
| rs554386851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147981215 | GTAAACGTTCCTCTT[A/G]ACATTGCTTTTGCCA | 79658 |
| rs554387993 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148005316 | AAGCTAGGTGTGCTG[A/G]CTCATGGCTGAAATC | 79658 |
| rs554401139 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147965193 | CTGGGTAGTGCTCTG[A/G]GATTTGTGACGGGTG | 79658 |
| rs554403067 | snp | C/G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147991960 | TCTATAGGTGAAGTG[C/G/T]GAATTGTCAGCCACA | 79658 |
| rs554405049 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147742944 | GGACAAAGCCAGAAG[A/T]ACAAGGGAATACAGT | 79658 |
| rs554424728 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147908803 | TTTCAAGTATACACA[A/C]ATTTTCAATAAGTCC | 79658 |
| rs554435274 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147969446 | AGCTCATGGAAAGAT[A/G]GCTACTGTTCATTTT | 79658 |
| rs554452707 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148046563 | GTGTGCTGCTTGGAG[A/C/G]TATTCTTGATTTCAT | 79658 |
| rs554463473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147949710 | GTACTGCCACTCTAG[A/G]AGATAGCTTTAAATC | 79658 |
| rs554469329 | in-del | -/TG | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147738239 | TAGCTTTTCTATATC[-/TG]TGTTCTCGTCAGTAA | 79658 |
| rs554474726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148031094 | TGAATTTTGAGACTG[A/G]CATTTTGGATCTACT | 79658 |
| rs554489086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147734110 | GGACTCTTTCTGTAA[C/T]TTGATGTTAACCAGA | 79658 |
| rs554492539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147749198 | GTGGAAATGAAGACT[A/G]TGATTCCTGTAGCTT | 79658 |
| rs554492625 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147742013 | TGAGTGTGATTTCTC[C/G]TGACTTGTTGACTTG | 79658 |
| rs554502267 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147956359 | TGCTCCAGCCAGTGT[A/T]AAGGTTCCTCCTGTG | 79658 |
| rs554503809 | in-del | -/T | 0.141258 | 0.225111 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147956751 | GGTTTTTTTTTTTCC[-/T]TTTTTTTTTTCTTTT | 79658 |
| rs554507891 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147988003 | CAGTGTGAGAAAATA[A/C]AGAGTGTGAGGCACT | 79658 |
| rs554508179 | snp | A/G | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147995175 | TCTCCATTGCTACCC[A/G]TTCTTGGCAGCCTTC | 79658 |
| rs554530677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147775014 | AGTTTCAAGTGATTC[C/T]ACTGCCTCAGGAGTA | 79658 |
| rs554531083 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147781481 | GAGCTACTTTTACAT[C/T]TTAAATACCGCCTTG | 79658 |
| rs554533878 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148003067 | AGTGCTATAAATTTC[C/T]TTCTACACACTGCGT | 79658 |
| rs554542002 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147975949 | CGATCAGTAGAATGC[A/T]TTGGTGCTCCTAGGT | 79658 |
| rs554545082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148054309 | GATTTAAGCAAACCA[A/G]GGATTTAAGCAAACC | 79658 |
| rs554550252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148027070 | GAGATCAAAGTGATC[C/T]TTGTTATTTTTCATT | 79658 |
| rs554567025 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147848061 | TTTTTATATTTGTAT[C/T]TTTTTCCCCCCACGT | 79658 |
| rs554571101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147859915 | TTTTTACAAACTTAC[A/G]TGCTCTCACTGAAGC | 79658 |
| rs554573490 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148034043 | GATCTCAGCAAATCT[C/G]TCTCTAAGCCTCACA | 79658 |
| rs554575149 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147810265 | TGTTATTTAAAACTT[G/T]CATTCTTTTATTACT | 79658 |
| rs554578272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147876550 | GTGAGCCAAGATCGC[A/G]CCACTGCACTCCAGC | 79658 |
| rs554591869 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147936575 | ACCTCATGATCCACC[C/T]GCCTCGGCCTCCCAA | 79658 |
| rs554607789 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147950416 | GGAGGTCTGGAGCCA[C/G]CCTGCCTGCCAGGGT | 79658 |
| rs554615012 | snp | A/G | | | upstream-variant-2KB | ARHGAP10 | GRCh38.p7 | 4:147730078 | TTTTATTGTAGATTA[A/G]TATTTCATTTTATGG | 79658 |
| rs554639649 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147909963 | GACCTCCTCAACATT[G/T]CTTGGACTACTGTAG | 79658 |
| rs554655379 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147777803 | TCATTTCTTTGAATA[A/G]TATACATGAAATTAT | 79658 |
| rs554657707 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148051884 | ACCATTTTTATTCTC[A/G]TCAATGCAATCACTT | 79658 |
| rs554661162 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147945112 | TAAGCCCAGCTTTGT[C/G]ATACCCATGCTGCAT | 79658 |
| rs554679919 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147854001 | ATGACAAATTTATAT[A/G]GTTTTTGACCTCTAA | 79658 |
| rs554693993 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147927250 | AGGGAAGATTTAAGT[A/G]TCACCCACTGAAAGT | 79658 |
| rs554694315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148040444 | CCTCCTGGGTTCAAG[C/T]GATTCTCCTGCCTCA | 79658 |
| rs554698469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148032917 | AGTCAAGTCCTCCAC[C/T]TTCTTCTGCCTGCTT | 79658 |
| rs554701532 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148047709 | CCAAAAGGGCATCAC[A/G]TTTCAAACAAGTGCT | 79658 |
| rs554706979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147825048 | CTCTGAACTGCCCTC[C/T]CTGTCACTGCAGCTG | 79658 |
| rs554719450 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147791408 | TGAGCCACTGCGCCC[A/G]GCCTCTTCTGTACTT | 79658 |
| rs554725043 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147909269 | GTGCACGGAGCCCCC[A/T]TGCCCTCAGTGGGTA | 79658 |
| rs554738350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147776241 | AAAAAAAATTCTAAG[A/G]CGGAGTCTTGCTCTG | 79658 |
| rs554741231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148048869 | AGCTTCCTATTCATA[C/T]GCATTTTAAAATGTC | 79658 |
| rs554746562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147956965 | GAGGTAATAAAATCT[A/G]TGGTGGTAGAAAATA | 79658 |
| rs554746979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147833172 | ATATGTGTGGTGATA[C/T]GGTTTGGCTCTGTGT | 79658 |
| rs554756605 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148007483 | AGTCACTTGGCTTAC[A/G]TAGCTTGATGAGGAT | 79658 |
| rs554756618 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148014349 | ATGCTGTGTTTTCCA[A/G]ATGTTTGCAGGTGCA | 79658 |
| rs554775118 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147849907 | TTCTAGCTTTTGTTC[A/G]AAAAGCCCTTTTGCT | 79658 |
| rs554780734 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147797309 | AGGTCTTTACACTGA[A/C]CCCAGCATGCCTTCT | 79658 |
| rs554781174 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148041506 | AGAACAGTTTGTCAT[C/T]ATCACAACAAAAAGT | 79658 |
| rs554789078 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147884896 | GCAGTGAGTGACAAT[G/T]ATATTTGTATTTCTC | 79658 |
| rs554804734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147952991 | CCAGTAGTTCTAGTA[C/T]GATTTGTAGGAGTGG | 79658 |
| rs554810316 | in-del | -/CTT | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148032917 | AGTCAAGTCCTCCAC[-/CTT]CTTCTGCCTGCTTTA | 79658 |
| rs554821658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147984441 | CTGTGGTGGTGCCAC[C/T]TTTAGCGGCTAATGC | 79658 |
| rs554822307 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147877005 | TAAATTGCTTGGCGC[A/T]TGAACAGGCGTGAAA | 79658 |
| rs554825853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147890091 | GTGGTTGCATAGACT[A/G]CTTTTGCTCACAGAC | 79658 |
| rs554855216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147883329 | GGCCTCCCAAAGTCA[C/T]AGGACTACAGGTGTG | 79658 |
| rs554862912 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889632 | CTTATAGCAATTTCT[C/T]AGTTGATTGTATATG | 79658 |
| rs554863343 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148054969 | TGTCAGTGACTGCAG[G/T]ACAGTAACCTTCAGA | 79658 |
| rs554866158 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148006414 | CTTGTCAGCCTGTTC[C/G]AGCTATTTCCCGTCT | 79658 |
| rs554871444 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147906086 | ACATTGATTTTGTAT[-/C]CTGAGACTTTGCTGA | 79658 |
| rs554893369 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147834185 | TAATCCATTAACTCA[C/T]TAGGCTGGGAATGGT | 79658 |
| rs554895166 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147841676 | TGTTGCTCAGTTGAC[A/G]TTGCCTTATTGAAAC | 79658 |
| rs554914774 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148015945 | TCTGTGAAATAAGAC[A/G]TCAGCACAGAGGACA | 79658 |
| rs554927885 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147745692 | GAGACGGGGTTTCAC[C/T]GTGTTAGCCAGGATG | 79658 |
| rs554939574 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147898921 | AGAGCAGCACGGGGG[A/C]ACCACTCCTGTGATC | 79658 |
| rs554944160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147951846 | GTTTCGGTAAGTTTG[A/G]TATATGTATACCTCT | 79658 |
| rs554947692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147884273 | TGGAACCACTCTCCA[C/T]CCCTCAAAGACATTG | 79658 |
| rs554956617 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147840853 | TCTTCCTTCCCAACT[A/T]CTGATTGGCTGCAAA | 79658 |
| rs554961190 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147754620 | TGTAATTGTATTCAA[-/T]TTTTTTTTTTTGTCT | 79658 |
| rs554964272 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147885967 | GGCATAATGCCACAA[A/G]TGGAGAATTCCATAC | 79658 |
| rs554966975 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147777759 | GTAAAAGGTGAACCA[C/G]GAGGTGTTGGGGGAG | 79658 |
| rs554969648 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147958282 | ATGGTGCTTAGTACG[A/C]GAATGACAACTAAAG | 79658 |
| rs554984965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147997893 | ATTAGTCCCAGTAAT[A/G]AGGAATTTTTAAAAC | 79658 |
| rs554995415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147771375 | TGTGGGTTATCTGTA[A/G]TATTTTGATACAGGC | 79658 |
| rs555001414 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147816128 | GGTCGCCAGCATTCT[C/T]GTCCTATCTCCCATC | 79658 |
| rs555001881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147866993 | CTGCTCTACAGTTGG[C/T]TGAGGCTTGGGAAAT | 79658 |
| rs555011607 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889934 | CTTGTTTGGGAAGCC[C/T]AGAGGTTGCCAGATC | 79658 |
| rs555023242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147825918 | AAGCAAAAGTCTCTG[C/T]CTTCATGGAGGTTAG | 79658 |
| rs555025947 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147738556 | AGACTCTGTCTCCCC[C/G]CCCCAAAAAAAATTA | 79658 |
| rs555042999 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148015661 | CTGTACTGTTCACGT[G/T]GTAGCTACTCTGAGG | 79658 |
| rs555056286 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147878296 | GAGACAGGGTTTCAC[A/T]ACGTTGGCCAGGATG | 79658 |
| rs555057790 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148024686 | TATAATTTCAGAACT[G/T]CCTTTTAGACACTCA | 79658 |
| rs555061890 | in-del | -/TAA | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148049599 | GTCTTCCCCATGCTG[-/TAA]TAATCTACAGGGAGC | 79658 |
| rs555066263 | snp | A/G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147868691 | TGGGGGTGGGAGAAG[A/G/T]TAGGGGATGGTTTCG | 79658 |
| rs555067670 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148057834 | TGTCACGGTTTCCTG[C/G]GTGTCCCCAGGGACT | 79658 |
| rs555070465 | in-del | -/A | 0.468148 | 0.122112 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147818566 | AGTGAAACTGTCACC[-/A]AAAAAAAAAAAAAAA | 79658 |
| rs555077139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148056521 | TACTACAGAGCTTCC[A/G]TAGACCCTTCACTTC | 79658 |
| rs555078479 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147895805 | GGCAGAAGTGGTGTT[A/G]TTGGCCATCTTGCCT | 79658 |
| rs555078742 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147947691 | TACAGGTGTGAGCCA[C/T]CATACCTGGCCTCAG | 79658 |
| rs555087844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147932121 | CACAATGAGATACCA[C/T]CTCAAGCCAGTCAGA | 79658 |
| rs555088004 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147886857 | CTCACCGCAACCTCC[A/G]CCTCCTGGGTTCAAG | 79658 |
| rs555126201 | in-del | -/A | 0.00597247 | 0.0543191 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147919566 | GGATCTTTTAAAAAC[-/A]ATTTTTTTTTCTTTT | 79658 |
| rs555130664 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147964679 | GTGGCGTGACCCAGT[C/G]ACTAGACCCCATCGA | 79658 |
| rs555131531 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147798889 | TCAGATGGGAAATCC[A/T]TTGTTCGAATTGGTG | 79658 |
| rs555146997 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147744617 | AGTCAAGACTTAGCA[G/T]CTGCAGGCTATAGGG | 79658 |
| rs555147932 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147752227 | TTATTGTCATTGATA[C/T]AGTATTTCACAGATC | 79658 |
| rs555158177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148070100 | AGGTGCTGGGTCTCA[C/T]GTTATATGTGTTACA | 79658 |
| rs555167902 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147812624 | CTCTTCTAATATTTC[A/G]ACATAGTCAAGATAT | 79658 |
| rs555184487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147805505 | TTTCTAATTCTATGA[A/G]GAATGTCAATGGTAG | 79658 |
| rs555189456 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147782537 | AGAACTGTGTACATC[A/G]CTGGGTCAAATGACC | 79658 |
| rs555192596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147979397 | GGTCTGTGTTCTGTT[C/T]CATTGGTCTATATAT | 79658 |
| rs555197074 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147847839 | ATGCAGTGGTTTTGC[C/G]ACAAGGAGCCTGAGA | 79658 |
| rs555204282 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147973417 | GTGGGTACATAGTTG[A/G]TGTATGTATTTATGG | 79658 |
| rs555213347 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148023026 | TGGAATGAATTATTT[C/G]ATATATAACAATCTG | 79658 |
| rs555218331 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147845710 | ATTTGGGATCACTAG[G/T]TGGGTAGATCCAGAT | 79658 |
| rs555231176 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148034842 | AGTAGTTTTGGGTTC[C/T]CAAGAATAATAACAC | 79658 |
| rs555245390 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147819021 | ATAATTCTTAGCACA[C/G]GTACAAAGCATGCTC | 79658 |
| rs555260804 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147977115 | GCAAAGAGAGCTCCT[C/T]GGAGCCTAGCTTAGT | 79658 |
| rs555265079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148062139 | GCAGGAGCATTGTGT[A/G]TAGGGAGACAAGTGG | 79658 |
| rs555265954 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147999424 | CAGCTGGAGCTGAGC[G/T]TTTGCTGGCTGTCCA | 79658 |
| rs555278763 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147836996 | GGCCTCCTATTTTTC[C/T]GTGCTGGAGGGCCCT | 79658 |
| rs555283947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147871956 | AAATAGAGAAAAATT[A/G]GCTGGAGGTGGTGGC | 79658 |
| rs555298876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147760430 | GAATCCAGCAGCTCC[C/T]GTGAGTCCACATCAC | 79658 |
| rs555316173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147916985 | AGGATACAGATTATG[C/T]GTTTGAATCTCTCAG | 79658 |
| rs555316912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147899037 | CTGAGTAGGACACAG[A/G]GTAGGTGGATTAGGA | 79658 |
| rs555321520 | in-del | -/TT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147959233 | AAAAAGCCCAGAGTA[-/TT]TTTTTTTTTTTGTTT | 79658 |
| rs555330830 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147845261 | GCATTCCTCACTGTA[C/T]TCCTACTTTTCTTCA | 79658 |
| rs555331280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147952492 | TGTGCTTTTAGTTTG[C/T]ACTTCTCTAATGACT | 79658 |
| rs555346942 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147897684 | TATATATTCTAATTC[C/T]ACATACACTATGAAT | 79658 |
| rs555346994 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147869775 | CCTGATCTAGGTGGC[A/G]TCTTTGTTCTTCAAA | 79658 |
| rs555350649 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147913045 | TAAATAATAATTGTA[C/T]ACTTAATGTTTTAAA | 79658 |
| rs555353844 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147905176 | ATTTTCTCCCATTTT[A/G]TAGGTTGCCTGATCA | 79658 |
| rs555354684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147924380 | CTTTTCTCTTTGTTA[C/T]CTATGGTTTTATACG | 79658 |
| rs555354899 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147865553 | GTATATATCATAATG[A/T]AAAGGATATTTCATG | 79658 |
| rs555356504 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147767554 | TATATTAAAAGATTA[C/T]CAAGAATCGTCTTGA | 79658 |
| rs555359314 | in-del | -/AT | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147932053 | ATGTGACCAACAAAC[-/AT]ATGAAAAAAAAGTTC | 79658 |
| rs555361824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148042969 | CTATTTCTTGTGGCA[A/G]TGGCAGTCCTGATGA | 79658 |
| rs555364825 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148047597 | ATATTAGGACAAATA[A/C]TATTAATACAAATAA | 79658 |
| rs555368999 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147879782 | CCCACTTAAGAGTGA[A/G]AATATGTGGTTTTAA | 79658 |
| rs555373179 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147750137 | AAAATTTTCATTCCA[A/G]AAGCTTTAAATTTGA | 79658 |
| rs555386957 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147980373 | GAACCACTGCTACAT[A/C]CCAGGAATAAAGCCT | 79658 |
| rs555390977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147987711 | ATGAGGTTGTCTCTG[A/G]GCTTTGGGGCTGAAG | 79658 |
| rs555395731 | in-del | -/T | 0.416545 | 0.186448 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148052393 | TTTTTGCACATTTGC[-/T]TTTTTTTTTTTTTTT | 79658 |
| rs555403532 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147862452 | TCCTGCCCTGATAAC[C/T]CTGTAGAAGTTGGGG | 79658 |
| rs555411140 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | ARHGAP10 | GRCh38.p7 | 4:147730907 | TTTTTTTTGAGACAT[C/T]GTCTCGCTCTGTCGC | 79658 |
| rs555425696 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147799104 | CATTGGTGTGATGTC[A/G]GCTCACTGCAACCTC | 79658 |
| rs555435873 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147949736 | AAATCCATTTTACTG[-/T]TTAGTAGACTCATAG | 79658 |
| rs555451219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147792668 | CTTTTCTTATTCTCC[A/G]TTATTATGATTTATC | 79658 |
| rs555452326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147987155 | TCACATAATATATGA[A/G]AAACTAACTTTTCTA | 79658 |
| rs555460457 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147971974 | CTGGGTTTGTAAGGG[G/T]TCTTGGGGAAGGTGT | 79658 |
| rs555462717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147798184 | CAGTAGCTTTATTTA[A/G]ATGTAGTGTGTGGAC | 79658 |
| rs555464158 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147849521 | ATAAAACAGTTTTCA[C/T]GTGGGGATTTAAGAA | 79658 |
| rs555466433 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147893335 | AGTGCTGGGATTACA[A/G]ACGTGAGCCACTGCT | 79658 |
| rs555467701 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147886171 | CTAAAATCCAAAAAA[A/T]ATTGAAATCCAGAAC | 79658 |
| rs555478378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147856347 | GTTGACCTATTGATA[C/T]GTATTTTAAATAGCG | 79658 |
| rs555482511 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147857878 | TTCATAGTAGTAAAA[-/T]TTTTGTTTCTGAGCA | 79658 |
| rs555492993 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147757814 | TCAGGCCTGGCTCAC[C/G]CTGGTCATTGGCCAA | 79658 |
| rs555497658 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147776691 | CTTTGTTTCCTTGCC[C/T]ATGTGACTTGAAGCT | 79658 |
| rs555505225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148071479 | AAATTAGCCAGGCAT[A/G]GTGGTGCGTGCCTGT | 79658 |
| rs555508258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147960498 | TATCTGTGATACATT[A/G]AATAAAATAGGTTGT | 79658 |
| rs555519323 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147893278 | GGTCAGGCTGGTCTT[A/C]AACTCCTGACCTCAG | 79658 |
| rs555520049 | in-del | -/TA | 0.0271762 | 0.113356 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147784477 | TATATAATTTATATT[-/TA]TATATATATTTAATT | 79658 |
| rs555523978 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148025830 | TTTTTTCTTATTTTA[A/G]TAGTGAAGTGACTTC | 79658 |
| rs555535628 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147947448 | GCTCTTTTTGCCCAC[G/T]CTGGAGTGCAGTGGC | 79658 |
| rs555540182 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147853921 | CTTTCTGCTTCCCAG[C/T]AAACAGTCATGCCAG | 79658 |
| rs555553990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147993357 | CGGCTAGGTGATGAT[A/G]TATGTAGGAGTTCAT | 79658 |
| rs555557049 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147765965 | TGAATACCCAAATCT[C/G]CAGATGCTCTCAAGT | 79658 |
| rs555561864 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147802352 | GCTTCTTAAAAAAGT[C/G]ATAGTGTGATGATGG | 79658 |
| rs555562782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147805003 | TTTGTCAATTTTTGT[C/T]TCTGTTGCAGTTGCT | 79658 |
| rs555562824 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148069573 | TTATTAATACCGAGT[C/G]TGTGCTTGCGCAAGT | 79658 |
| rs555576253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147868826 | GAATCTGATGCCACC[A/G]CGGATCTGACAGAAG | 79658 |
| rs555580506 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147763208 | TATATTTTAATTGGT[C/T]TGATAATCTGTAAGT | 79658 |
| rs555589824 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147801990 | TTTCTCTCCCTGAGG[C/T]ACAGCAAGAACTAGG | 79658 |
| rs555593281 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147945332 | TTTTCTTTAGAACTT[A/C]CTAGCCGTTTTGAAT | 79658 |
| rs555602447 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147796976 | TGATTGTAGGATGTA[G/T]TTTTCCTCTTTCTCT | 79658 |
| rs555615981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147898479 | TTTTTTGCCTTGCCC[A/G]GGGTTCCATTGAGGT | 79658 |
| rs555617770 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147810182 | CATTACAGGCGAGAG[A/G]TCATTTACCCTTGCT | 79658 |
| rs555624399 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147861438 | TTCTCTCCTTCTCGT[C/T]GCCCACAATGTAGTG | 79658 |
| rs555633552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148044695 | GGCTGGGGAAAGCTG[A/G]AGGCCAGCCCCTCGC | 79658 |
| rs555641076 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147890729 | CTACTCGGGAGGCTG[A/C]GGCAGGAGAATCACT | 79658 |
| rs555644085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147820451 | CCACCACGCCCGGCT[A/G]ATTTTTGTGTTTTTA | 79658 |
| rs555676549 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147954229 | TTAAGTTGGTTGATA[C/T]TTTTGTTCAAATCTT | 79658 |
| rs555706895 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147732528 | TCTCTCGGCAGGAGA[C/T]GGAGGGTCTTGTGTC | 79658 |
| rs555709715 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147992117 | AGTCCCTCAAAAGCG[A/C]TCCTTGTTTTAGCTT | 79658 |
| rs555717372 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147989430 | CTCTTCCTAATAAGC[C/G]TGGGAGCGGTATGGG | 79658 |
| rs555738800 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148016685 | TTCAGTTCCAACACC[A/G]TCTACCTGGAGGTAG | 79658 |
| rs555748453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148031961 | AACAAACATCTGGTC[A/G]TGGATTGGTTGTAGT | 79658 |
| rs555750099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147781362 | TTGACCAAACTGGGA[C/T]ATGATTTCATATTTA | 79658 |
| rs555759956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147828223 | ATTAAAATGTTAAAA[C/T]TACATATGTCTATTT | 79658 |
| rs555778834 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148009921 | GCTTTTGTGAAACCT[C/T]AGTTTCTGGTATCTG | 79658 |
| rs555781585 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147933946 | GTCCCCTTAGGATCT[C/G]TTGTGGGGCAGAGGT | 79658 |
| rs555781668 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147941148 | AGATGGTGTTATGAT[G/T]ATTAGAACTGGAAGA | 79658 |
| rs555819505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147937526 | AACTTAAAAAATAAG[A/G]AATAAAAAGCAAAGA | 79658 |
| rs555820099 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147940486 | TGTGAATGACAAAGC[A/G]CTTTTACATTACACA | 79658 |
| rs555831181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147821107 | CAACTATACGGGGCC[A/G]CTGAGCCAGGAGTCA | 79658 |
| rs555838277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147913603 | GTCTCTTTTACATGT[C/T]GAAGTTTCTTCTTAT | 79658 |
| rs555838357 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147907294 | ACTATTGAAACACTA[C/G]TTTCATTTTGATGGA | 79658 |
| rs555857176 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147994672 | AACATTGCTTTATTC[A/G]TAGATTGAAAATGGA | 79658 |
| rs555857760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148038605 | CCTTGGGTACAGCAT[C/T]ATTAGAAGAGACACA | 79658 |
| rs555872261 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147860292 | CTAAAAATACAAAAA[A/G]TTAGCTGGGTGTGGT | 79658 |
| rs555878165 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147948986 | AAAAAAAACAAAAAA[A/C]CCCCCAAAAAACAGA | 79658 |
| rs555882131 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148000682 | CTGATGACCAGTGAT[C/G]ATGAGCATTTTTTCA | 79658 |
| rs555882322 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147768463 | GTTAGTAACGTAACT[G/T]GCCAAATTCCTTGCC | 79658 |
| rs555887592 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148037026 | TAGGTGAGATAGGTG[A/G]TTTTTCTGTGTTCTT | 79658 |
| rs555887722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147806205 | TCCAGAGTCCAGGCG[A/G]CTTTCCAGGTCGGAT | 79658 |
| rs555899901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147813690 | TAATGGCAGAGGCCC[A/G]GGGAGAAGATCTCAG | 79658 |
| rs555918387 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147906541 | TATTTTACCACAGAT[A/G]AAAGTAAAAAAAAAA | 79658 |
| rs555918824 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147995228 | GATAACCAGTTTTTA[G/T]GTTTCACATCCTTTT | 79658 |
| rs555923451 | snp | C/T | 9.9226e-05 | 0.00704295 | synonymous-codon, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147946660 | GGAGAATTCTGCAGA[C/T]TGGGAAGTGAAGACA | 79658 |
| rs555939347 | in-del | -/TG | 0.00993419 | 0.0697739 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147933424 | GCTTGTGACAGTGTC[-/TG]TGCATTGAGGGATTA | 79658 |
| rs555955155 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911650 | TACAGGCGTGAGCCA[C/G]CGCGCCTGGCCTCTT | 79658 |
| rs555964221 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147992727 | GCCTTTTAATAAAAA[A/G]GTTTAAAACAATTTC | 79658 |
| rs555984642 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARHGAP10 | GRCh38.p7 | 4:147731726 | GGACTAACGACTGCA[A/G]TTAAGACGCTCCTTC | 79658 |
| rs555994019 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148004679 | GGCCTTTAGTCCTGC[A/C]ACTGCAAGGAAATGA | 79658 |
| rs555997300 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147778651 | CTAATCAAAATGTCC[C/T]ATTCCTGCCTGGGTA | 79658 |
| rs556000518 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147959758 | ACATATTCTTAATCC[A/G]GGTTTTGACTCTATT | 79658 |
| rs556001453 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147894300 | TTTTCATTTTAGCCA[A/G]TTTTGACTAGAGATG | 79658 |
| rs556022354 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147981025 | ACCAACTTTTCATTT[C/T]ATTGATCTTTAGTAT | 79658 |
| rs556023399 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147829713 | TTGTACTTATCTGAG[G/T]TGGGCAGCTGTCCAG | 79658 |
| rs556039847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148043786 | TATATGTATATATAT[A/G]TGTATATATATATGC | 79658 |
| rs556041644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147967760 | TGCCTGGGGGATCTG[C/T]AAGGCTTTTCTGTAA | 79658 |
| rs556050878 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147872616 | ATCAGAAGCCTCACC[C/T]ATAACAGAAATAGCT | 79658 |
| rs556059881 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147919041 | CTTCCGAAGGTGGCT[A/C]AGTTCTCCTTACCTC | 79658 |
| rs556062555 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148043415 | ATCACTCAGAAGAAA[C/T]GATAGGTGAAAAATA | 79658 |
| rs556068908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147827569 | TTTAGTAAGCCCATA[C/T]CCCCGACACCGGGAC | 79658 |
| rs556074356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147876050 | CAGGACTTTCAATCC[A/G]ACCTAAAAATTTAGT | 79658 |
| rs556092025 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911563 | GAGACGGGGTTTCAC[C/T]GTGTTAGCCAGGATG | 79658 |
| rs556093591 | snp | A/G | 1.64743e-05 | 0.00287 | missense, utr-variant-5-prime, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:147822775 | CACTCAGAGACTTTA[A/G]GTTTGAGTTTATCGG | 79658 |
| rs556099321 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148055058 | CAAGCTAAAGTTCAG[A/C]CCTCTTACCTGATTC | 79658 |
| rs556130948 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147970207 | GCTTGTGCAGGAAAA[C/T]TTCATATGGATGCGT | 79658 |
| rs556153969 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147746805 | ATGTCTACACACTCA[A/C]ATTGTAGATTTATGG | 79658 |
| rs556155633 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147794634 | TCTGGAAATTGAGTT[A/G]TATGGTACATATTTT | 79658 |
| rs556171944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147863882 | CACAAGGGTTTCAGT[C/T]TCTTGACATCCTCAC | 79658 |
| rs556172568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148065439 | GTACTCTTCAGAGAC[A/G]GAGACTCCTGGTAGT | 79658 |
| rs556177352 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147876468 | CGTAGTGGCGGGCAC[A/C]TGTAGTCCCAGCTAC | 79658 |
| rs556207141 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147800745 | TTCCAGGGTTTATAG[C/T]GCTTAGTAGGGAGGA | 79658 |
| rs556214811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147735002 | TGTCTCCTGTTTGCA[C/T]TACATTCTTGGAAGA | 79658 |
| rs556217598 | in-del | -/A/AA | 0.476562 | 0.11997 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147906547 | CCACAGATAAAAGTA[-/A/AA]AAAAAAAAATGGTTA | 79658 |
| rs556218253 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147968587 | GAATAATCTCTTAAG[C/T]GACTTGCTTTCTTAC | 79658 |
| rs556220552 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148045682 | GGCGGAGCTTGCGGT[C/G]AGCCGAGATCGCGCC | 79658 |
| rs556227453 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147753741 | ATATTTGAGAGAATG[A/G]TTTTTTTCCCCTTTC | 79658 |
| rs556253454 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147869309 | TGAAACTCCTTGCAC[A/G]GCTCGTTTATTTGTG | 79658 |
| rs556261606 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147919788 | GTTTCACCATGTTGG[C/T]GAGGCTGGTCTTGAA | 79658 |
| rs556263089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147955056 | TTCACAAAGCTACTT[C/T]CCGTGATTAGATATG | 79658 |
| rs556269120 | in-del | -/A | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147900534 | GACTTGCTGTATGTG[-/A]TGAGTTATCCAGAGC | 79658 |
| rs556285448 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147928621 | TGCTGTTCAAATAAT[C/T]ATCATCCGGGGAAGA | 79658 |
| rs556289631 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147961553 | TTGTCATAAGGAAAA[C/G]TATTATCCTTTTGAA | 79658 |
| rs556306715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147747618 | GAGAAGTTCTTTGCA[C/T]GTGTTTCTAGAGCTA | 79658 |
| rs556308539 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147931585 | CAAGGCACCATAAAA[C/G]CTATTAAAAGCAAAA | 79658 |
| rs556314973 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147934948 | AAGGGGATTTTTATC[C/T]GGTTTTGAAGGTTTA | 79658 |
| rs556319291 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147766308 | TGGGTAAAAAAGGTC[A/G]TATTTGCATATAACC | 79658 |
| rs556322229 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147935917 | GCATTAGCAATTACT[C/T]CTCTCAGGTTGATGA | 79658 |
| rs556340865 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147741094 | TCATTTAGTTCAACC[G/T]TTTTTTCCTACAAGT | 79658 |
| rs556341284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148011108 | ACATAGATGATGCTG[A/G]TTGTTCTAAGTGCAT | 79658 |
| rs556364530 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147975517 | GGAAAGCCCAAGGTT[G/T]ATGAGCTGCATCTGC | 79658 |
| rs556384421 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147801201 | TAAAACATATCTCTC[A/G]GGGGTCTTATGGAGG | 79658 |
| rs556385365 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147906046 | TTGTCTATTATTTGT[C/G]TATAAGAATGCTTGT | 79658 |
| rs556388833 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147748689 | AAAAAGCAGTAGATA[C/G]GCTGGGCACTGTGGC | 79658 |
| rs556400263 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147986911 | GGTGGATTCTTAAGC[C/T]CTAGACTCTGCTGCT | 79658 |
| rs556403162 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147969583 | AAATACTGGCTCTGG[A/G]TCTTGCTCTTGGATA | 79658 |
| rs556407903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147835705 | TTTAACAGTTTATTG[C/T]CTTAGTATGCACGAG | 79658 |
| rs556409733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147843182 | GCCAACCCTCCATGC[A/G]TGCTCAGCATCCCAT | 79658 |
| rs556425788 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148012160 | TTCAGTTAAGGGGAT[A/G]TGCCTGACAGTGTGT | 79658 |
| rs556426589 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147894192 | TTGACTTCTCAGGCA[A/G]TTAAGGTTACAAAGT | 79658 |
| rs556431706 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147809019 | CTGGCTGTAGTGTAG[C/T]GTGCGATGTTAATCA | 79658 |
| rs556465236 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147881375 | GGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 79658 |
| rs556467392 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147763917 | ACGCCGCCATGCCTG[A/G]CTAATTTCTGTATTT | 79658 |
| rs556467617 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148041912 | GGGAGATCCCTCAAC[A/G]TTCTTTTACTTTTCC | 79658 |
| rs556480374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147970056 | AACCTAAATTTCCCC[A/G]TTACCTCGCCTTGTC | 79658 |
| rs556492966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147921779 | GTCCCTCCCACCTGC[C/T]GTCTCTGTGTGACAT | 79658 |
| rs556500942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148012889 | CAAAATTTTGTAGAA[A/G]TGTTCCTTTGTAGGG | 79658 |
| rs556503137 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147743018 | CTCTGCCATACTGAT[C/G/T]GATAGTTTTTTTTTT | 79658 |
| rs556504601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147850683 | TCACTGCGAGGGTCC[A/G]CGGCTTCGTTCTTGA | 79658 |
| rs556504719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148069642 | TGTGCAGGTGAGACT[A/G]TATTTGAGACTCTCT | 79658 |
| rs556508610 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147802139 | TCTTCTTTCCATATG[C/G]ACTTATTCCTTTTGC | 79658 |
| rs556509293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147877667 | CATGTGAAGTTCCAG[A/G]TGCTAGAGGTCCCTC | 79658 |
| rs556533314 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147942320 | GGAGAGCTGCCATTT[A/G]TCCAATTCTCTGTAG | 79658 |
| rs556560671 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147756385 | TAAAAACAGTTACAC[A/T]CTCTAGAGTGGGCAT | 79658 |
| rs556579503 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148006512 | TCCTAGCATAATAAA[A/G]TGGTGGTGGTCTGCC | 79658 |
| rs556581873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147790384 | CGCAAACATTCAGTT[C/T]GTAACACCTAGTAAT | 79658 |
| rs556582725 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147980466 | GAGGATTTTTGCATC[C/T]GTGTTCATTGGAGAT | 79658 |
| rs556583753 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147782458 | ATACTTTGTGGAAAC[A/T]GTTGTCAGCAGAAAG | 79658 |
| rs556594124 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147749367 | TAAAGAATTAAATAG[C/G]AGTTTACTGGCTTAA | 79658 |
| rs556594454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147901855 | AGAATATACAACCAT[C/T]TATCTTGAGTTAATA | 79658 |
| rs556611280 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148067291 | AAGCAGGGTTTATCT[C/G]TGTGTGTGTTTGCAC | 79658 |
| rs556624761 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147852829 | GTTCAAGTGATTCTC[A/G]TGCCTCAGCCTCCCA | 79658 |
| rs556624857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147814395 | TTGGCTTTGATTGGG[A/G]ACTAAGTTTCTCATT | 79658 |
| rs556631795 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148067084 | GGAAAATACCTTGTG[G/T]ATGTGTTGACACTCT | 79658 |
| rs556633792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147802801 | AGTTGTTTCTCATCA[A/G]TCTTGAAGACTCCTT | 79658 |
| rs556642611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147789964 | AAGGTGTGTTCGTAA[C/T]GAACAGAAAGGTGTG | 79658 |
| rs556644147 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147844571 | TCCCACAAATAAGTG[A/G]GAACATGTGATGCTT | 79658 |
| rs556645148 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148064732 | TTGATTACTCTCTGA[A/C]CCATCTCATCTTGTG | 79658 |
| rs556649481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147984570 | CTGTTTTCACTGGCA[A/G]GGTGTCTGTTTGAGT | 79658 |
| rs556656783 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147733813 | TGGATGATCTCCAAG[G/T]TTCCTTTTGGTTCTC | 79658 |
| rs556660511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148019796 | ACAAAAAACAAAAAA[C/T]GTCTAACCTAACCTT | 79658 |
| rs556661509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147937928 | AGGTTGCAGTGAGCC[A/G]AGATTGCTCCATTGT | 79658 |
| rs556670037 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147764067 | GCCTGGCCCAGACAG[G/T]GATTCTTGATCTTTA | 79658 |
| rs556713890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147976330 | GAGAGAAAAATAAAT[A/G]TCTTAAACAACAACA | 79658 |
| rs556721581 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147850803 | CTCTAAGGCCTAGCT[A/G]AGTTCTTATTTTCTT | 79658 |
| rs556735268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147831052 | CAGGCCCACCCCAGA[A/G]CTCTACTGAGTCAGA | 79658 |
| rs556738427 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147755522 | GAGTGAAACTCCGTC[A/T]CAAAAAAAGGGAAAG | 79658 |
| rs556748968 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147762955 | GTAATGAAGGATAAC[A/G]AAAGACTTTTATGGT | 79658 |
| rs556751063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147754951 | AATGCAAAAATTAGC[A/G]GACGCCTATAGTCCC | 79658 |
| rs556764764 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148039189 | TATATTGCTTCTTTT[A/T]TTTAAATACTTAAGG | 79658 |
| rs556770754 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148072650 | AGGACCCCACACTCA[C/T]TGCACTGGCAGCGTG | 79658 |
| rs556774572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147949506 | CTGGTTTGCAGTGCT[C/T]CTGGCATCTGGTGGC | 79658 |
| rs556781875 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148033855 | TCCTGTTAGACTTCA[C/T]GTGACTTTCACCTTT | 79658 |
| rs556786126 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147818335 | CTTTGGGAGGCCGAG[A/G]CAGGTGGATCACCTG | 79658 |
| rs556790891 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147923567 | TGGCATTAAAATGTC[C/G]ATCTAGGCAAGCTGT | 79658 |
| rs556796213 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148068243 | GACCCCACGTGGCAG[C/T]GGCAGCAGCAGCGGG | 79658 |
| rs556804799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147957068 | TCACCTGTTGGACCA[A/G]TACCTTGTGTTTTGC | 79658 |
| rs556818217 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147962791 | ACCTCAGTCTCCTGG[A/G]TAGCTGGGATTACAG | 79658 |
| rs556871742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147943827 | CTAAAGGACTGCTAG[A/G]GATGATTGAGCTATT | 79658 |
| rs556876502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147831668 | TACAATTGGACAGCA[C/T]TGCTTTTTCTTACAA | 79658 |
| rs556877272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147845776 | AGTGTGCCTTAAGTT[A/G]TCTATGAGACACTGT | 79658 |
| rs556882602 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147736454 | AAATAATTTTCCTAT[G/T]TTGTAAACTTGAGCC | 79658 |
| rs556886826 | snp | A/C | 0.0618563 | 0.164627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147905543 | AGATCAGATAGTTGT[A/C]GATATGCGGCGTTAT | 79658 |
| rs556904835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147950427 | GCCAGCCTGCCTGCC[A/G]GGGTTGGAGCCCCAG | 79658 |
| rs556910154 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | ARHGAP10 | GRCh38.p7 | 4:148073251 | AGACCTTCCTGGAGG[A/G]GCCTTCACCCTTGAC | 79658 |
| rs556910602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147990231 | AAGCACAAATGCTGC[A/G]TTTAGTTAGTGATAA | 79658 |
| rs556927175 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147952577 | GTGAAGTGTCTGTGC[A/G]TATCTTTTTCCCAAT | 79658 |
| rs556932449 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147937469 | TGAATTTGTGGGGAT[A/G]CAATTCAGCCTATAA | 79658 |
| rs556940306 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147853089 | TCAGGGTCGCAGGTG[A/G]CTAGAGCCCATTTCA | 79658 |
| rs556942103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148028898 | TATTCGCCACAGATT[A/G]GGCTCATAGGTAAAT | 79658 |
| rs556946433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148068880 | GCCTCTCTTTGGTGC[C/T]ACTTGGGGTCCCTGC | 79658 |
| rs556949830 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147776300 | TCTCGGCTCACTGCA[A/G]CCTCTGCCTCCTGGG | 79658 |
| rs556958404 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147876807 | GCACTGTGCTAAATT[C/T]GTATACAACTTGTCT | 79658 |
| rs556974848 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148025220 | TAATTCGTTAAAATT[A/G]CTTGATTTTTAAGGG | 79658 |
| rs556979463 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148020918 | TTACACTCCCATTTT[C/G]TGGTGTTTTGATTTT | 79658 |
| rs556987861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147990658 | AGCTGGAGGTCTATT[A/G]AGTGAACTAACATAG | 79658 |
| rs556991711 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147846859 | AATGAATGTGATAGA[C/T]CCCTTTGTTGTTTAC | 79658 |
| rs556992969 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148003700 | GATCTTTGTTGGTTT[A/G]AAGTCTGTTTTATCA | 79658 |
| rs557003193 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147998077 | GAAAAAAATGAAATA[A/C]GCATTCACCTACTCC | 79658 |
| rs557006987 | in-del | -/A | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147988683 | TGCAACATGATCCAT[-/A]AAAAAAATGGGGTCT | 79658 |
| rs557014981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147824243 | AAGAGAATTGCTTGA[A/G]TCTGGGAGATGGAGG | 79658 |
| rs557017891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148021611 | TATTTCCTGGCTTTT[C/T]TTCTCTCCTTCACTG | 79658 |
| rs557019094 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147743675 | CCAGCTACTCTGGAG[G/T]CTGAGGCAGGAGAAT | 79658 |
| rs557025930 | in-del | -/C | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147988747 | TTAGTGTTGACTTTT[-/C]CCCCCACACTTCCGT | 79658 |
| rs557026073 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147804017 | TTTTTTTTTCTTTCA[C/G]GTTCAGGGGTACATG | 79658 |
| rs557035732 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147904694 | CCACAATAAACATAC[A/G]TGTGCATGTGTCTTT | 79658 |
| rs557046082 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147790191 | CGCCACCTTCTTGCT[A/G]TGTCCTCACTTGGGA | 79658 |
| rs557049627 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147971080 | CCTGGGTGACAAGAG[C/T]GAGACTCTGTCTCAA | 79658 |
| rs557053645 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147825528 | ATTTTGAGGTAATTT[G/T]TGTGTATATATTGTA | 79658 |
| rs557064473 | in-del | -/ACTT | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147985919 | ATTGAGGCTTCACTC[-/ACTT]TTACCAGCCAGATGC | 79658 |
| rs557066087 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147844523 | ACCCTTCTACTCTCT[A/G]TCTCCATGAGTTCAA | 79658 |
| rs557084625 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147817480 | AATCAAGGACAAGCA[G/T]TGGCAGTTCAGGCCA | 79658 |
| rs557085417 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147803604 | CCCATGCTTCCCTAC[A/C]TCTGGTAACCACCAT | 79658 |
| rs557090876 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148041118 | ACTAATATATTAGAT[A/C]TTTTCTTTTTATGCA | 79658 |
| rs557096700 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147979543 | ATTCCATGTGAATTT[C/T]AGAAAAGTGTTTTCT | 79658 |
| rs557099574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147810524 | TATATTAACCATCTG[A/G]ACGTTTACATCTCAT | 79658 |
| rs557126062 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147895983 | GTGTCTCTTGAAATG[A/G]TCATTAAATATGTTT | 79658 |
| rs557128865 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147992225 | CCTAAGCCTGATTGC[A/C]TGCTGTCGTTCGGTC | 79658 |
| rs557129622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148034063 | TAAGCCTCACAAATT[C/T]GGACAATAAAACTTT | 79658 |
| rs557131352 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147776849 | CAGCAAAATGCAGTT[C/T]GTCCAGATGCTGTGA | 79658 |
| rs557153159 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147909861 | GTCAAGCTGTTGCTG[G/T]GAGCTTACTCTCTGC | 79658 |
| rs557162784 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147878901 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTAAGACTA | 79658 |
| rs557162896 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148003140 | CATTGGTTTCAAAGA[C/G]CATGTTTATTTCTGC | 79658 |
| rs557170545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147871995 | GTAGTCCCTGTACTC[A/G]GGAGGCTGAGGTGGG | 79658 |
| rs557176817 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147785296 | TTTTATTTCTTCTGT[C/T]GTGTCTCCAATCCAG | 79658 |
| rs557189631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148002341 | TGAGGATTTTTGCAT[C/T]AATGTTCATCAGGGA | 79658 |
| rs557195296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147885449 | GGAAAAACCCATTCC[C/T]ATGATTCAGTTACCT | 79658 |
| rs557199585 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147878341 | ACTTCGTGATCCACC[C/T]GCCTTGGCCTCCCAA | 79658 |
| rs557201029 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147825103 | CCTGGGTGGTGGCTG[G/T]TGGGGGTTTATGTTG | 79658 |
| rs557210602 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147916766 | ATAGCTGCGGGGGCA[C/T]ATCTAGAGGGTAAAG | 79658 |
| rs557219799 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147977766 | CCCATATGGTGAACA[C/T]AGTACTCAACAGGAA | 79658 |
| rs557239117 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147756507 | GGTTTCAGTTACCCA[G/T]GATCTGAAAATAGTA | 79658 |
| rs557249160 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148001588 | GTCCTCTTTTATTTC[A/C]TTGAGCAGTGCTTTA | 79658 |
| rs557253788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147745246 | TTGCAGAGGGCTGAG[A/G]AGGGAGTGTGAGGAA | 79658 |
| rs557256496 | in-del | -/GG | 0.0103295 | 0.0711199 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147841839 | TTTTATAAATGAGTT[-/GG]GGATATAGTGTTATT | 79658 |
| rs557257594 | in-del | -/AGACTC | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148044994 | CTAGACTTTATAAAT[-/AGACTC]AGACAAGAAGAACTG | 79658 |
| rs557259937 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147947110 | CAACATGTCAATGCA[A/G]AGCTCTTTGAAAAAG | 79658 |
| rs557260071 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147915145 | TGAAACTAGTGTGTA[C/G]GATATCGGCGGAGTA | 79658 |
| rs557289571 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148051483 | TATCGGGCATTGCTA[A/T]CTGCTTCCTCTACAG | 79658 |
| rs557299041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148035567 | TATAGTTCCCATTTT[A/G]TCTTGCCATGTTTCA | 79658 |
| rs557301485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147828441 | CAGTTCAACAAATAG[C/T]GTGTGCCTGCCACAT | 79658 |
| rs557303763 | snp | G/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147835584 | TCACCATGTTGGCCA[G/T]GCTGGTCTCAAACTC | 79658 |
| rs557317567 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147791804 | TGGCCAGGCTCGTCT[C/T]GAACTCCTGACCTCA | 79658 |
| rs557323078 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147765559 | AATCACAGCACTTTG[A/G]GAGGCCAAGGTGGGC | 79658 |
| rs557329936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147797933 | GCCATCTCATCCCAT[C/T]CCTCTCCTCTTTGTC | 79658 |
| rs557334120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147926082 | TGGTAGTGGTGAGTG[A/G]GTGGTATGATGTGGG | 79658 |
| rs557350701 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148000003 | ACATATGTATACATG[C/T]GCCACGTTGGTGTGC | 79658 |
| rs557352355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147751520 | AGGCGCATGCTACCA[C/T]GCCTGGCCATTTTTT | 79658 |
| rs557369784 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147861481 | GGAGGATCACCCCTG[A/T]TTGTGTTACAGCTCT | 79658 |
| rs557409084 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147923007 | TTGCACACATAGTAA[A/G]CACTCAGTAAGCATT | 79658 |
| rs557415996 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147839698 | AATGTAAAGTTGTTG[C/G]AGTGGTTCCTCCCCA | 79658 |
| rs557420174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147952629 | TATTATTATGTTTTA[A/G]AAGTTAAAAAATATA | 79658 |
| rs557433699 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147918321 | TTTGTATTTTTAGTA[C/G]AGACAGGGTTTCACC | 79658 |
| rs557447802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147739806 | AATGGCATGATCTTG[A/G]TTCACTGCAACCTCC | 79658 |
| rs557451151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148050827 | CCCCTTTATCTCTGC[A/G]TACCAGCTATACAGT | 79658 |
| rs557454351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147910612 | AAATATTCAAGGACA[A/G]CGATCTTCACATGCC | 79658 |
| rs557456827 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147952115 | CACTGCTAACTAATG[C/G]ACCATTTTATAGATA | 79658 |
| rs557462342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148009629 | AAGAAATTAATTCAC[A/G]TGTTTCTAGTGAACT | 79658 |
| rs557469326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147827433 | AGTGCGCCAGCAAAG[A/G]TAATGTGGCTCACAT | 79658 |
| rs557469576 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147925361 | ATGTTTCCCATCTCT[G/T]CAGCAGAGGAATGAA | 79658 |
| rs557489551 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148050231 | TGTGATATTGATGTA[A/G]TTATTAGTGAACATT | 79658 |
| rs557493364 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147916276 | TTACCTTTTCATTTC[A/T]TGTCTTTCTGTTTTT | 79658 |
| rs557510552 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147932779 | ATGTAACCTGTACAT[A/C]CTGCACATGTACCTC | 79658 |
| rs557512512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148023070 | TTAAATTTAATCAGA[A/G]ATTTTATTTTGGAAT | 79658 |
| rs557523798 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147873396 | ATAGCATCCATACAT[A/G]TATGGCATGCACATA | 79658 |
| rs557525280 | snp | A/T | 0.0174175 | 0.0916809 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147793324 | TATATATATATATTT[A/T]TTTTTTTTTACAAAT | 79658 |
| rs557548407 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148049556 | CCTGACCTATCTTAA[C/T]GGTCTAATTTAATCT | 79658 |
| rs557549161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147932247 | GTGGAAGACAGTGGC[A/G]ATTCCTTAAAGACCT | 79658 |
| rs557559715 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148064650 | GGATTAAGCGGCTGC[G/T]TTAGGCTCCCAGACC | 79658 |
| rs557560884 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147833334 | GATGGTTTAAAAGTG[G/T]CAGTTTACCCTGAAC | 79658 |
| rs557591169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147923463 | ACCATTTAAAACTAA[A/G]TTTGGATGCCACTTT | 79658 |
| rs557608042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147899345 | TGTGTGTGTGTGTGT[C/T]TGTGTCTGTGTCTGT | 79658 |
| rs557617065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147841846 | AAATGAGTTGGATAT[A/G]GTGTTATTTGCCACA | 79658 |
| rs557652579 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147894461 | AACAAATCATTTACC[A/G]GATATAATAATAGTG | 79658 |
| rs557656141 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147797320 | CTGACCCCAGCATGC[C/T]TTCTATGTTCCTCAC | 79658 |
| rs557658516 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147971023 | GCTTGAACCCAGGAG[A/G]TGGAGGTTGCAGTGA | 79658 |
| rs557675604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148022388 | AACGTCAGCCCTTTG[A/G]AGATGCAGCTTCTAT | 79658 |
| rs557675712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148029665 | TCTCCATGCTTACCA[A/G]TTTTTTTTTGGCATG | 79658 |
| rs557680822 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147750957 | TCATTGTGGGCAGGT[C/T]GCGTGAGGTCAGGAG | 79658 |
| rs557682052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147974125 | TCCAAAGTATTCTCC[A/G]TAGGGGTACATTCCC | 79658 |
| rs557686468 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147939691 | TGTTAAACACTTGAT[G/T]TTTTCAAAGGTTATT | 79658 |
| rs557694613 | snp | A/C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148054381 | CTGCCCCTCTGGGCC[A/C/G]GGGTGAGGTTTCCAG | 79658 |
| rs557697190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147960165 | ATTAAGAACTGGATT[A/G]TAATTTATTACCTAA | 79658 |
| rs557701185 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147745787 | TGAGCCACTGTGCCC[A/G/T]GCCTTTTTTTTTTTT | 79658 |
| rs557701274 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911578 | CGTGTTAGCCAGGAT[C/G]GTCTTGATCTCCTGA | 79658 |
| rs557706682 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147892305 | AATTTAAAAGAGTGA[A/G]TTAAGAGCATGTTGC | 79658 |
| rs557712209 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147919413 | GAGTCACATCAACTC[A/G]TCTTTCATCCGTTTA | 79658 |
| rs557716153 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147890501 | ATGAAATGGTCAAAA[G/T]ACCTGAATTTAGACA | 79658 |
| rs557717511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147787851 | AGCAGCAGCGTGACT[A/G]GAGTTAATGTGAGGC | 79658 |
| rs557721266 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147946484 | TTTTAGAGAAATCAT[A/T]TATATAATGTTTTCC | 79658 |
| rs557726357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147931128 | TGGGTGATGTGAGTA[A/G]TGCTCTATGACAGTG | 79658 |
| rs557729161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147868885 | TCCTGCCATGTGACC[C/T]GGTTCCTAACAGGCC | 79658 |
| rs557753348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147753787 | ATGCTCACGTATTCA[C/T]GAATGTTGAAAATTT | 79658 |
| rs557761395 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148066288 | TTACCCATCCTCACA[G/T]CCCAGTATGCAGAAC | 79658 |
| rs557762326 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147776212 | AAATTGCCCTTTTGC[A/G]AATGAATGATGGAAA | 79658 |
| rs557779212 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148004336 | AAACAAATAGTCTTC[A/T]ACAGGTGGAAGAAAC | 79658 |
| rs557788033 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148071524 | AGGAGGCTGAGGCAG[C/G]AGAATTGCTTGAATC | 79658 |
| rs557792550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148009355 | CAGTCTGGTCTCCAA[C/T]TCCTGACCTCAAGTG | 79658 |
| rs557812404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147881376 | GGCGCGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 79658 |
| rs557816303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148004815 | CTCCAGAGCAGAAGA[C/T]ACAGTTTAGCTGTGC | 79658 |
| rs557816840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147827422 | ACAATATACAAAGTG[C/T]GCCAGCAAAGATAAT | 79658 |
| rs557817169 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148058476 | AGGGGCTTGTATCTC[C/T]AGTGCTGCCCAAAGC | 79658 |
| rs557825802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147843207 | TCCCATCTCCTCCCG[C/T]GTCAGAGATTTTGAA | 79658 |
| rs557833278 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147754884 | GGATCACCTGAGGTC[A/G]GGAGCTCGAGACCAG | 79658 |
| rs557837698 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147745713 | AGCCAGGATGGTCTC[A/C]ATCTCCTGACCTCTT | 79658 |
| rs557845432 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147981137 | TTGTTTTTCTGGTTT[A/C]TTTAGGTACAAGGTT | 79658 |
| rs557846645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147794722 | TATTCCATTATCTCC[A/G]TTTTACAGATGAGGA | 79658 |
| rs557847427 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148072301 | GGGAATGTCAGGATT[C/T]GCAAAATGGACTTTT | 79658 |
| rs557853167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147880613 | ACTTAGAGATCTTCA[C/T]GTTCTGGAAAATGTT | 79658 |
| rs557860855 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147746405 | CTGCGCCAGGCCTGC[-/T]TTTTTTTTTTTTTTG | 79658 |
| rs557863973 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147849608 | GATCTTTCCCCGTCT[C/T]CTGTTTCCCATCTGA | 79658 |
| rs557871506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147972607 | AGCCAGAAGAAACCC[A/G]GGCAGGATCAGGTCA | 79658 |
| rs557871866 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147856964 | TTCAAGTGATTCTCA[C/G]GCCTCAGCCTCCTGA | 79658 |
| rs557879293 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147934535 | GACTAAGATTGTGGA[C/G]TTGTTTTAAGATGTA | 79658 |
| rs557882041 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147798560 | CTAGGTGGGTGGATC[A/G]CTTGAGTCCAGGAGT | 79658 |
| rs557899404 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148058001 | TTTCTCTGCACTGCT[C/G]TTGTCCCTCGGTGTG | 79658 |
| rs557911306 | in-del | -/ATA | 0.0850919 | 0.187897 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147784746 | ATATATATTATAAAT[-/ATA]ATATATTATAAAATG | 79658 |
| rs557912224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147973066 | GGCCTAATGGTGACA[C/T]TTCTGTTGAGAGCCA | 79658 |
| rs557913461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147887473 | ACTACAGCCACCATC[A/G]CCAATGAAACCACCC | 79658 |
| rs557917415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147941319 | TTGAAGTGCTAAGCT[A/G]TCTCAAAATTTGTTG | 79658 |
| rs557921012 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147948065 | CCTGCCTCAGCCTCC[A/T]GAGTAGCTGAGATTA | 79658 |
| rs557924706 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147772328 | TGCCAGTTGACACTT[C/T]ACATCACACAGTTTG | 79658 |
| rs557930645 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147752847 | TACTATTAATGCTGA[C/T]CTGGGCCTTTGATTA | 79658 |
| rs557954585 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148015796 | GTATTTGGCCATTTT[C/G]TAACTATGCTCTTTT | 79658 |
| rs557958122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147954852 | TAAAGATAAATTCTT[A/G]TTTTTATAATATATT | 79658 |
| rs557962417 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147792647 | TTGTGGTCCTCTGGG[A/G]CCTTGCTTTTCTTAT | 79658 |
| rs557962682 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148064291 | CTTCCACGTTAATTT[C/T]TCTTTTGGGAGGAGT | 79658 |
| rs557964812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147798991 | AGAAGACTAGTTATT[A/G]ATGTTTACCATTGAT | 79658 |
| rs557973046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147886246 | CATTGCCAATTCTGC[C/T]CTTTTTACAAGTCTT | 79658 |
| rs557982869 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147733275 | AGAGTCTTTCTAGGA[A/G]AGAAGGGGCCAAAAT | 79658 |
| rs557987325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147939081 | ATTTTCTTACCCTTA[A/G]TGCTACTCAGTTTGC | 79658 |
| rs557988981 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148022835 | GTATTTGCAGTCATA[C/T]GTTTCTGTTTACGTA | 79658 |
| rs558003699 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147985794 | TCTGTAAGCTTTTCC[C/T]CAAGTTAGCTCCAAG | 79658 |
| rs558004226 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147758785 | GGAGTTCGAGACCAG[C/T]GTGGCCAGCATGGTG | 79658 |
| rs558007098 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147855521 | AAAGAGTGACTATTA[A/G]GTAAAAGAGGTTAAA | 79658 |
| rs558017575 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147801786 | TCCACAGACATCAGA[C/T]ACCTCTCAAAATAGT | 79658 |
| rs558038072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147829130 | GATCTCAGCTCACTG[C/T]ACCCCTGCCTCCTGG | 79658 |
| rs558038368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148037844 | GTCTCAAAAAAAAAA[A/G]AAAAGAAAAGAATGG | 79658 |
| rs558062419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148045540 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTTAACA | 79658 |
| rs558070369 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147836612 | TTATAGCACCTGAGC[A/T]CCTGTGTCCCAGTTA | 79658 |
| rs558072889 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147732592 | TCCGGACCAGCCCAG[C/G]TCTCTCGGAACCCCG | 79658 |
| rs558079653 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148031045 | GCCTGGGTGACAGAT[C/T]AAGACCCCATCTCCA | 79658 |
| rs558091028 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147902548 | GAGTTTGAGACCAGC[C/G]TGGCCAACATGGAGA | 79658 |
| rs558094490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147978886 | GTGTCTGTTCATGTC[C/T]CTTGCCCACTTTTTA | 79658 |
| rs558096459 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147991219 | GCCCGCTTCTCTGGG[-/T]ATGTTAGCGGTCCTT | 79658 |
| rs558102735 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148070189 | GTATGCCTGCACACA[C/T]GCACACAGAACATGT | 79658 |
| rs558110021 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147994083 | TCCAAAAGGGATTTC[A/G]GGCAGCTAAGCCACA | 79658 |
| rs558111507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148006908 | CCCACCCCAGCACAC[A/G]TGCTTTGCTTATCAG | 79658 |
| rs558111769 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147735993 | TTCTCATAAATTTTA[C/T]GTTAGGCAGTCTTGA | 79658 |
| rs558145108 | in-del | -/TG/TT/TTTT | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147869999 | AAAAAGTCCCAGTTT[-/TG/TT/TTTT]GTGTGTGTGTGTGTG | 79658 |
| rs558149671 | snp | A/G | | | missense, nc-transcript-variant | ARHGAP10 | GRCh38.p7 | 4:148047036 | GAGGGAGCTTTGGAG[A/G]CTGGGCATCCACTAT | 79658 |
| rs558165393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147960668 | AGTATACAGCTTAAT[A/G]AATTTTCACATGTAA | 79658 |
| rs558172951 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148041223 | GAGGAGCATGGGATA[C/G]CTTTGCTGATGTGGG | 79658 |
| rs558185733 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147964241 | CACTTCAGTTCCGAG[A/T]ATCAGCAACTAGGGA | 79658 |
| rs558195645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148001153 | GCCAGTTTTCCCAGC[A/G]CCTTTTATTGAATAG | 79658 |
| rs558197572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147995373 | AAACCCTGGCTCTAG[A/G]TGAAAACAGCAAGGG | 79658 |
| rs558219122 | snp | C/T | 9.22694e-05 | 0.00679162 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147857679 | TTTATTTTTCTGTTA[C/T]GTTTTCAAAATTTGA | 79658 |
| rs558227392 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147801407 | CTGTAATGCTCTGGG[C/G]TTTATAATGTTAACA | 79658 |
| rs558238130 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147770848 | AGCTTAAATAGCAGT[A/C]TTATTTTCTAGTAAT | 79658 |
| rs558259106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147943044 | ATGAGTTGTCTTTAG[A/G]TGAGTCATGGTTTTT | 79658 |
| rs558267340 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147762575 | TTGTTCTGTCTCCCA[G/T]GCTGGAGTGCAGTGG | 79658 |
| rs558267951 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147768312 | CTATCTGAGGATGGC[A/C]GTACTTACATTACTT | 79658 |
| rs558284843 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148011630 | AGCAGTCAGGAGCCT[G/T]TGCAGATTTGGGAAA | 79658 |
| rs558286782 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148049611 | GCTGTAATCTACAGG[A/G]AGCCTCTAAAGAGAT | 79658 |
| rs558302082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147809263 | ACCTTTCTTCAAATA[A/G]TCGACAGTCAAAATT | 79658 |
| rs558303260 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147807356 | TAGGTGATTGTATTA[C/G]GTAATAAAAAGTATG | 79658 |
| rs558304854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148030441 | TTAAGGCTGTCAAGA[A/G]TGACTGATTTGAAAC | 79658 |
| rs558312214 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147989478 | ACCTCTGCAATCTTG[A/C]CCATAAGAGACAGGT | 79658 |
| rs558314092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGAP10, MIR4799 | GRCh38.p7 | 4:147781462 | ACACATTTAAAAATA[C/T]GGGGAGCTACTTTTA | 79658 |
| rs558322836 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147955823 | CTCGGATCTAAATTA[C/T]AGACAGAAGGAATAT | 79658 |
| rs558322882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147863996 | TAATGATGAGCGATG[C/T]TGAGTGTCTTTTCAC | 79658 |
| rs558325990 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147886141 | AAGATACCTCATTTC[A/G]TATGTGCAAATATTC | 79658 |
| rs558333599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147906988 | TCATCTAAATTCTCA[A/G]TTTCATCTTTCCTAC | 79658 |
| rs558359497 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147792734 | CTTTTGTAGTGTCTG[C/T]TCTGTTTTGCTTATG | 79658 |
| rs558384973 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147966392 | GACTTTGGTGTCTGT[A/G]GGGATTCTGGCATCA | 79658 |
| rs558389071 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147751417 | CACCCAGGCCAGGGT[A/G]CAGTGGCGTGATCTC | 79658 |
| rs558394894 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147774197 | TTATTATCTTGGTAC[A/C]TGTTAAATTCCTATA | 79658 |
| rs558396232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147882697 | TCAAAGGTGAATTCT[C/T]TTTTTTCCTTATTGC | 79658 |
| rs558402232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147876087 | CATGACTCAGGGAAC[A/G]GTTACAGGGTATCTG | 79658 |
| rs558403437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147773651 | CAGTTATCTGTTTTT[C/T]GTGGGCAGAACTTAA | 79658 |
| rs558403550 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147896271 | TTTTTTCATAAATGT[A/G]TGTGTCATATTGGTA | 79658 |
| rs558415449 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147974787 | TTTAATGGGCTCATG[C/G]TTCCACAGGGCTGGG | 79658 |
| rs558430391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147962181 | GTGTTTCTGTCTGTT[A/G]GTGGAATTGGCCCTG | 79658 |
| rs558431573 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147747663 | TTTTTTTGTGGAAAG[C/G]ATAGAGTTTAAAAAT | 79658 |
| rs558434141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147820574 | AGGCGTGGGCTACCT[C/T]GGCCAGTTTTTTTTT | 79658 |
| rs558462558 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148037087 | CTTATGGTAACTTTG[A/G]GGATCTGGTCACCCA | 79658 |
| rs558463342 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148005973 | AAAGTAGCCACAAAT[G/T]TCTTTCACACTCCTT | 79658 |
| rs558478641 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147791403 | AGGCATGAGCCACTG[C/T]GCCCGGCCTCTTCTG | 79658 |
| rs558478861 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148048629 | GGAATTTAGCATGTG[C/T]GTATGTTTTAGTGAA | 79658 |
| rs558489459 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147915661 | TTTATGTTAGCTTTT[C/G]TCATTTAAAAATAAG | 79658 |
| rs558506985 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147982786 | ATATGTTTTCCAAGC[G/T]GCTTATTTTCTCTTC | 79658 |
| rs558522329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147769525 | AATTCCTTGTTAACT[A/G]ACATTGTTTCCCGGG | 79658 |
| rs558525403 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147949939 | AGTACATAGGATTTC[G/T]TTTTGGATCTTGATA | 79658 |
| rs558527127 | snp | A/G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147857257 | CATTCGGTTGGTGAG[A/G/T]GGTGAGTGACGTGGA | 79658 |
| rs558530761 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148033397 | GAATGAAAAAAGCAA[C/G]TTTTAAGATGGAATT | 79658 |
| rs558531187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148011211 | GGTTATTTATCAGAG[C/T]ATAGCACATCACCCC | 79658 |
| rs558534055 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147922853 | AATGTGCATGTGCCT[C/T]ATTTGGCAGTTATAT | 79658 |
| rs558539297 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147788536 | CCAGTCCTTGGTGAG[A/T]TTAGGGGTGAGACCA | 79658 |
| rs558539944 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147822558 | AGAGGCTACCCAGAG[C/T]GTGCCAGGTTGAAGA | 79658 |
| rs558541057 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147864513 | GTGAGTTTTTCAAGA[A/G]GAGAAGTCCCTTTGA | 79658 |
| rs558552612 | in-del | -/A | 0.490591 | 0.0679425 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148071642 | AACAAACAAACAAAA[-/A]AAAAACACAAAAAGC | 79658 |
| rs558552772 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148033451 | AGGAAAACCTATATA[-/T]TTAAATATAAGCATA | 79658 |
| rs558567722 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147858992 | CACTTCTCATGACTC[A/G]CTCTTCTCCAAACCC | 79658 |
| rs558576894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147871486 | TCAGATTTAAAATAC[C/T]AAAATAATAAGGCTT | 79658 |
| rs558588187 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148013601 | GCTGAGGCAGGAGAA[C/T]GGCGTGAACCCGGGA | 79658 |
| rs558616952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148038684 | GTTTTGATTGGGTGG[C/T]CCTATTTAAAAGATA | 79658 |
| rs558646325 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147909398 | GTGGGTAGGGCTGAA[A/C]GAAATATCAGTGGGT | 79658 |
| rs558648826 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147956299 | TGGGACCAATGTTAC[C/T]GCTGCCTGAACATTG | 79658 |
| rs558650467 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147949074 | TCTGGTTGTCCCACT[A/T]TTTAATGATATAAAA | 79658 |
| rs558661352 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147923314 | GTACAAATGAGCCGC[A/C]CCCCATGAGCAGTGC | 79658 |
| rs558670703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148001675 | ATTCTCTTTGAAGCA[A/G]TTGTGAATGGGAGTT | 79658 |
| rs558672499 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147785058 | GTTGATTCCAAGATG[A/C]TGAAATGTATGGACG | 79658 |
| rs558674670 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147865619 | AGGATTCATTTTAAT[A/T]TTAATATCGACTTAT | 79658 |
| rs558676030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148054150 | ATAAATTGGCTGTGT[C/T]TCAATATCTAAATAA | 79658 |
| rs558682527 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147770864 | TTATTTTCTAGTAAT[C/T]CTGGAGGCTAGAAGT | 79658 |
| rs558686775 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147791361 | AGGTGATCTGCCTGC[C/T]TCAGCCTCCCGAAGT | 79658 |
| rs558696428 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147741898 | GAGTCACACCCCAAG[G/T]TGCTGCCATAGCTAG | 79658 |
| rs558710068 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148055169 | CTGTTCTCTTACAGC[A/G]AAACCAAGAACTTTT | 79658 |
| rs558710530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147872536 | GGTTAGCACCCCTGC[A/G]CTATTGGATGTCTGC | 79658 |
| rs558711034 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147787844 | GGAAGACAGCAGCAG[C/T]GTGACTGGAGTTAAT | 79658 |
| rs558711138 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | ARHGAP10 | GRCh38.p7 | 4:147731981 | AGAGAAGGGGACGAG[C/T]GGGAGCGCGGGCCCG | 79658 |
| rs558718376 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148039324 | TGAATATATAATTCT[C/G]TGCTCAAATTTTTTT | 79658 |
| rs558744007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147928799 | TCGTGCCTGGCTATT[C/T]TGAAATTAATTTTGA | 79658 |
| rs558745394 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148006384 | GAAAATGGTGGGAAC[A/G]TCAAATATATGACCC | 79658 |
| rs558750121 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148013004 | AATATAATGTGTATT[A/C]TCACCTTTGTAACAT | 79658 |
| rs558762138 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148055188 | CCAAGAACTTTTGCT[C/G]TAAGAGAGTGGACTT | 79658 |
| rs558785695 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147919957 | GACTGGGAAGTAGGA[G/T]TCTTTAAATTTCCGC | 79658 |
| rs558801904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147836742 | ACATTAGTTTCTCTA[C/T]TGGGAAAATTAGATT | 79658 |
| rs558804014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147967829 | TCAGAATCACCTGAG[A/G]GCCTCTTGTAAGTGG | 79658 |
| rs558809365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147963518 | TTTATTGATTTATTT[A/G]ATAGTTTTCCAATCA | 79658 |
| rs558815955 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147888099 | CATCACACTCCCTCT[C/T]GCATCACTGGCTTCT | 79658 |
| rs558829009 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148038527 | ATCCTTTCTCCTCCC[C/T]TACCTCCTGAACCCT | 79658 |
| rs558862774 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147790044 | CTTAGCTCAGGCTGC[C/T]ATAACAAAATACCAC | 79658 |
| rs558874153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147964110 | CCATTCCTGGAGATA[C/T]TAAACTTCTGCAGGC | 79658 |
| rs558888489 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147737002 | GGTAAGTGGCATAGC[A/G]CGCTAACTGAATCTG | 79658 |
| rs558909522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147763906 | ATTACAGGCGTACGC[C/T]GCCATGCCTGGCTAA | 79658 |
| rs558910788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147957715 | CTGAGAGTTCTCAAG[A/G]TTTCTCCTGGGTCCC | 79658 |
| rs558911786 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147744776 | GAGGGCAAGGTATTT[C/T]GTAGTAGCCAGGAGA | 79658 |
| rs558917631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148062079 | AGAGCTGTGGCAGAC[A/G]GGGTAGGCTGCTGGG | 79658 |
| rs558918706 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147932505 | CATGTTCTTTGCAGG[A/G]ACATGGATGGAGCTG | 79658 |
| rs558930125 | in-del | -/C | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147959519 | CTATCCCTCCCCGCT[-/C]CCCCCACCCCACGAC | 79658 |
| rs558931537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147927778 | AAGGCGCAGAGGCTG[C/T]GAGATACTCCTTTTG | 79658 |
| rs558934115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147883616 | TTTCCCCAAGGTCAC[A/G]TAGCTAGTGGGTAGT | 79658 |
| rs558937031 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147936065 | TTGCTTGAATGCAGA[C/G]TATGATTTGCTCTTT | 79658 |
| rs558963222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147983128 | CTCAGAAGATCCACC[C/T]GCCTTGGCCTCCCAA | 79658 |
| rs558974586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147743890 | TGCCTGAACCATAGT[A/G]AACTCTCTCTGTGTT | 79658 |
| rs558983639 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148062684 | AGGAAGCCTGAATCC[A/G]GTGGCATTTTCTTCT | 79658 |
| rs558984337 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147960687 | TTTCACATGTAATCA[A/G]CCCCAGATCAAGCAA | 79658 |
| rs558984551 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147779275 | ACAGCCTGGCACCCA[A/C]CTCCAGGGACCACTC | 79658 |
| rs559002470 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147970239 | GATCTATGTTAGCCA[C/T]GGGTTTCCCTGGCAG | 79658 |
| rs559003408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148062511 | GATTAACACGCATCA[A/G]TTATTTGAACTCTCC | 79658 |
| rs559010502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147877989 | TCACCCAGGCTGGAG[A/G]GCAGTGGCACGATCT | 79658 |
| rs559017260 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147757338 | AGCTGGGACTACAGG[C/T]GTATGCCGCCATGCC | 79658 |
| rs559020774 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147884214 | GACCTTGATCATGCC[A/C]AATTTTCTTTTCTTT | 79658 |
| rs559036905 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147874134 | TCTAACATTTTGCCA[C/T]GCTTAGGACCCTTGG | 79658 |
| rs559045352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147832735 | AGAGATGAAAATAGA[A/G]TCTTTCACATCTTCT | 79658 |
| rs559051642 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147940560 | CCCACCCCAAAACAG[C/G]CTGCCTCTTGAAGAG | 79658 |
| rs559054857 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147995701 | CAAAATTTCCAAAAA[-/T]TTTGCATGGTCCATC | 79658 |
| rs559066546 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147785346 | TCTGTTCTCTGGTCC[A/C/T]GGATTTGACATGTAT | 79658 |
| rs559067518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147845207 | CACTACTTTGAAGAA[A/G]CTCTCTTTGCACACA | 79658 |
| rs559072455 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147821406 | TTTCACCTTATGCTT[C/G]GTGCTTTTCTTCTAT | 79658 |
| rs559072506 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147749866 | CTTAATTGATACTGT[C/G]TAAAAGGCTTGAATG | 79658 |
| rs559081166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147970088 | CTCCCATTTCATCTT[C/T]GAACACTTCTACTCC | 79658 |
| rs559098732 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147942591 | TCTCTCCGTCCTCCT[C/T]CTCCTGCCCCTTTGT | 79658 |
| rs559106225 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147839150 | TCTATCTATCTGTCT[A/G]TCTGTCTATGTATAT | 79658 |
| rs559115119 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147845464 | TAAAATAGATAAATA[G/T]TTAAAGTTTATTAAG | 79658 |
| rs559118701 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147872424 | TTGGTAGGAAGTCAT[A/G]GGTTTTCAAATATAT | 79658 |
| rs559148348 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147976554 | TGGTTTTTTTTTTTT[C/T]TTCTTCTTCTCAGCA | 79658 |
| rs559149449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148055563 | GCATGGTGGTATGCA[C/T]CTGTAATCCCAGCTA | 79658 |
| rs559153056 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889500 | AGATGGGGTTTCACC[A/G]TATTGGCCAGGCTGG | 79658 |
| rs559154160 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147756100 | GTTGCAAGATGGCCT[A/C]GTCATTACACCCACC | 79658 |
| rs559170795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148068380 | AAAGGTCTCAGATAG[A/G]CACAGAATAATCCCT | 79658 |
| rs559171707 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147885080 | CAGTAGAGGGTGAAG[A/G]AGTGGGGAAGGTTTC | 79658 |
| rs559182779 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147990083 | CAGCCTTCTGCCTGA[A/T]TGAGGAGGAGGAAAG | 79658 |
| rs559184268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147749452 | TGTTAAGAAAAACTA[A/G]TTTTTGTGGGTATCA | 79658 |
| rs559197252 | snp | A/G | | | intron-variant, missense | ARHGAP10 | GRCh38.p7 | 4:147854816 | ACCATACCATATATG[A/G]ACGAAGATATTTCTA | 79658 |
| rs559199836 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147963849 | ATTCCAGCCTCTGCT[A/G]TGACAGGACAACCTC | 79658 |
| rs559216703 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147852153 | CTTGCCAAACAGGAG[G/T]TGCTCAGCTTTTTGT | 79658 |
| rs559217432 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147983659 | CTAGAAGTTCTGTTT[G/T]GTTCCTTCTTAACAT | 79658 |
| rs559220189 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147805782 | TCACACCACTGCATC[A/G]TGGGCAACAGAGCAA | 79658 |
| rs559237027 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147914811 | GTTTTAAATTTAGGG[A/T]AAACTAATTCCTCCG | 79658 |
| rs559261088 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148009203 | TGGTGTAATATAGGC[C/T]CACTGCAACCTCTGG | 79658 |
| rs559262709 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147973668 | CCCATTAACCATCCC[C/T]GCTCCCCCCGCCACT | 79658 |
| rs559264134 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147746206 | CCTCCGGGGTTAAAG[C/T]GATTCTTCTGCCTCA | 79658 |
| rs559280281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147850605 | AGAAGGAAGAAACTC[C/T]GGACACATCTGAACA | 79658 |
| rs559287075 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147737398 | GGCCTCATGTGATCC[A/G]TCCACCTCGGCCTCC | 79658 |
| rs559288011 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148014793 | CGTATAGAGTGCTAC[C/T]GAAATCAATATGGTA | 79658 |
| rs559299469 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147954290 | ACTGAAACAGAGAGG[G/T]GTTTAACTCTCTGAT | 79658 |
| rs559300472 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147810560 | ATACAAATTCTGGAA[G/T]TGGTGGTGCAGAGTT | 79658 |
| rs559300927 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147759432 | TAAAAAACAGGTGAA[A/G]GTGTAATGGCATGTG | 79658 |
| rs559303774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147923897 | TTTTACCAATTGCGC[A/G]TTAATTTTAAATTGC | 79658 |
| rs559306336 | snp | C/G | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147975591 | GAACATGTGAAAAAG[C/G]AGTGACAGACAGAGT | 79658 |
| rs559313526 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148002678 | TTTATCCATTTCTTC[C/T]AGATTTTCTAGTTTA | 79658 |
| rs559331836 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148062258 | ACGGTGCTAGTTCTC[C/T]GGCAGGGGAAACAAT | 79658 |
| rs559339424 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147783890 | AACACACATTAAATT[A/G]TGTATTATATTTATA | 79658 |
| rs559355424 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147778665 | CTATTCCTGCCTGGG[C/T]ATAGCCTTAGAGTAT | 79658 |
| rs559370744 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147915944 | CCCTGTCTGTATAAA[A/C]ATTTTTTTAAAAAAA | 79658 |
| rs559375144 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147807889 | GTCCAGAAAAAGTTC[A/C]TGAAGGTCCTCGTCC | 79658 |
| rs559377840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148025868 | AATCTAGTTTGTGTT[A/G]AAATATGCATTATTA | 79658 |
| rs559402085 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148055990 | AATCCAGGGGTGAGC[A/G]AACCGTGGCCCACTG | 79658 |
| rs559416935 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147890992 | ACAAGTACTGGCAAG[A/G]ATGTAGAGAAATTGA | 79658 |
| rs559428475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147838809 | GCTTTATAAAATTAC[C/T]GAATACAAAATTTTG | 79658 |
| rs559447141 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148021942 | TATGGGACTATAAAG[C/G]AAATGCTGTCTTTGA | 79658 |
| rs559453911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148022488 | GAAGGAAGCCTCTGA[A/G]CTGGGGTCTCACAGC | 79658 |
| rs559456919 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147889869 | GGTTGCATGTAACAG[A/C]AAAAGTCAAAACAAA | 79658 |
| rs559464000 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147913678 | CTCCCATCTCTAAAT[A/G]CAGTCACATTCTGAG | 79658 |
| rs559467594 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148068980 | TTCCTGGACTGAGAC[C/G]TGCAGGCATAGGGAG | 79658 |
| rs559470190 | snp | A/C | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147816299 | GAAGGATTCTTCATA[A/C]TTATTTGGCTATTTT | 79658 |
| rs559474279 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147932392 | ATTGCAAAGACATGG[A/C]ATCAACCCAAATGCC | 79658 |
| rs559490321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147898011 | GGCGCCTGCCACCAC[A/G]CCTGGCTAATTTTTT | 79658 |
| rs559505664 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147796952 | GGCTTGTTGATTTTA[C/G]CTCTGAAATGATTGT | 79658 |
| rs559508890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147772226 | TTCCCAGTTGGCAGG[A/G]TTATCTGAGACTTCT | 79658 |
| rs559510625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147991095 | TTACACCAAACCCCC[A/G]TGACACACAATTTGT | 79658 |
| rs559512309 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147755844 | GTCAGCCTCTGTGGC[A/T]GTTTGCTGTGTATTT | 79658 |
| rs559512851 | in-del | -/TTT | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148034484 | ACCACTCCCGGCTAA[-/TTT]TTTTTTTTTTTTTTT | 79658 |
| rs559516150 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148027036 | CCCCCAAATACAAGG[A/C/G]AAGTTCAGGAGGCTA | 79658 |
| rs559526788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148058727 | CTGCTGATCTGTTCC[A/G]TTTTCTAAAAATACA | 79658 |
| rs559541839 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147752030 | AGCTAGGACTATAGG[C/T]GTGCGCCACCACACC | 79658 |
| rs559549455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147991570 | TCCTTTACCTAGTGT[A/G]TACCAAAATTCCAGG | 79658 |
| rs559551580 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147747199 | CCGATTTTCTCTTTT[A/G]TCTCACCGGAGTCAT | 79658 |
| rs559561523 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147990315 | ACAGTAACATCCTAC[C/G]TAACTAAACATTTTG | 79658 |
| rs559570616 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147997276 | GTAAACTGTACATCA[A/G]TAATCTATTTTGGAA | 79658 |
| rs559587640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147777517 | CTGCCTGCCTCCCAG[A/G]GTGCTGGGATTACAG | 79658 |
| rs559591381 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147805135 | GTCTTTAATTCATCT[C/T]GAGTTAATTTTTGTA | 79658 |
| rs559592221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147861406 | CTAGGTCTGGGCTCC[C/T]CGAAGGGCCGCAGCT | 79658 |
| rs559593607 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147985862 | TGCGCGGATCCCTAG[C/G]AGTAAGGGAAATGAC | 79658 |
| rs559603432 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147983980 | TTCTTGATTTTTTTA[C/T]TCTTTTTGTCCTTGG | 79658 |
| rs559614093 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147796510 | TTCATCTCTTTTTTT[C/T]CTTATTTCTTTTTTT | 79658 |
| rs559616936 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147765645 | TCTTTACAAAAAATA[C/G]AAAAATTAGCTGGGT | 79658 |
| rs559622141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147803658 | CAACTTTATTGGCCC[A/G]CACATTTGAGTGAGA | 79658 |
| rs559626459 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147872907 | TCAGCTGTATGTACA[A/T]CTGCTTCCTAAGGCT | 79658 |
| rs559626877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147763428 | GCGATTCTCCTGCCT[C/T]AGCCTCTCGAGTAGC | 79658 |
| rs559634886 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147775166 | ATCCACTCGCCTCGG[-/C]CCCCCCAAAGTGCTG | 79658 |
| rs559660062 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147904801 | AGATCCCTGAGGAAT[C/G]GCCACACTGACTTCC | 79658 |
| rs559674911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148037251 | AATTGGAAGTCTTGA[A/G]TGTTCCACTGTCCAT | 79658 |
| rs559684391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147803209 | AGATGGGGTTTCACC[A/G]TGTTGGCCAGGCTGG | 79658 |
| rs559687505 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147861198 | CCACTGTGCACAGCC[G/T]GGCATGCCGACTGTG | 79658 |
| rs559691754 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147840406 | ACTCACATGAAACAT[C/G/T]TAGTTTTTTTTATTT | 79658 |
| rs559696404 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147910641 | CCACTGCTGTACTTG[A/C]AGAAAATGAAACATG | 79658 |
| rs559716084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147947601 | AGAGGTGGGGTTTCG[C/T]CATGTTGACCAGGCT | 79658 |
| rs559716733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147931531 | AAATTCAAGTCAGAT[C/T]AACCTAGCTATACCT | 79658 |
| rs559716786 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147835491 | GATTTTCCTGCCTCA[G/T]TCTCCCTGAGTAGCT | 79658 |
| rs559729658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147867304 | CTTTCTGCCAGGTCT[C/T]GGATAAAGAGATTTA | 79658 |
| rs559750096 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147965579 | AGAAATTAGCCCTTT[C/T]TTTAAGTATAGAGAT | 79658 |
| rs559759232 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147938389 | AAATAGTATATGTAA[C/G]TATAATTTTTAAAAA | 79658 |
| rs559761387 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARHGAP10 | GRCh38.p7 | 4:147730308 | GTCTCAGCAGCCCCT[C/G]TATGAGAAAAGGTTT | 79658 |
| rs559774055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148049714 | ATATTTGCCTTTTAG[C/T]ATTATTTGATATTTA | 79658 |
| rs559776868 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147847978 | AAGTAACATTTGCAT[G/T]CTGTTGACCATTTTT | 79658 |
| rs559792716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148044134 | TGTTTGGCAGGAAGG[A/G]AGAGAGAACTCTCTT | 79658 |
| rs559797681 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147738267 | GTAAAATAGAAATTG[C/T]AGGGCTGGGCGCGGT | 79658 |
| rs559801150 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147978359 | GACTTTTTAAATAAT[C/T]GCCATTCTGACTGGT | 79658 |
| rs559807780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147939121 | CAAAAATGTCTTTTC[A/G]TCATTGATTTGTTCA | 79658 |
| rs559809056 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147804467 | GCGATGAACATAAAT[A/G]TATGTGTGTCTTTAT | 79658 |
| rs559814161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148034378 | GCTAGAGTGCGATGG[C/T]GCGATCTTGGCTCAC | 79658 |
| rs559815776 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148016919 | GGGAAGCTGCAGCAG[A/G]CAGATCACTTGAGGC | 79658 |
| rs559822511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147958413 | AGTTGGGAAGCAAAA[C/T]GATTACCACAAAGGT | 79658 |
| rs559825717 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147971710 | AAGAGATTCGGGCCA[C/G]GTGTGGGAGGTTGAG | 79658 |
| rs559828866 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148036473 | TGTTGTTATTGTGAT[A/T]GTGAGTGACTTCTCA | 79658 |
| rs559845836 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147937715 | TCAGGCGTATTGGCT[C/T]ATGCCTGTAATCCCA | 79658 |
| rs559855711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147820219 | GAACCAAGAGCAACC[A/G]GTGTGTCTAGATCTT | 79658 |
| rs559871530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147811594 | ATGGCTTTTTTTAAA[A/G]AAAAAAAACAAAAAA | 79658 |
| rs559885965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147764866 | AGTGTGTTTTATATG[A/G]CAGATGTGCTGAGGA | 79658 |
| rs559886409 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147917889 | TCAAAATGATGAATA[A/C]GATGATGAAGATACC | 79658 |
| rs559890574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148009387 | TCTGCCCACCTTGGC[C/T]TCCCAAAGTGCTGGG | 79658 |
| rs559890691 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147903251 | TTTTGGTCTTCTATG[C/T]ACCTTCTCAGCTTAG | 79658 |
| rs559895968 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147911504 | AGTAACTGGGACTAC[A/G]GGTGCCCACCATCAC | 79658 |
| rs559904077 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147904339 | TGCATCCATTAACTC[A/G]TCATTTAGCATTAGG | 79658 |
| rs559911354 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147947304 | ACAAGTATATAGACA[A/G]TTAAAAGAAAATGAA | 79658 |
| rs559920504 | in-del | -/AGGCAGGGGCGGATCATGAGGTC | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148037602 | CCCTTTGGGAGGCCA[-/AGGCAGGGGCGGATCATGAGGTC]AGGAGATTGAGATCA | 79658 |
| rs559945535 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148048125 | ACCATGCCCAGCCCA[C/T]CCAGAGAGTCTTCAA | 79658 |
| rs559953563 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148043291 | GTCTGTTCATAAATC[C/T]TTTGGTACCATTTTT | 79658 |
| rs559954203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147999541 | TGAGGCGCCCATTGC[C/T]GCTCTGGATCAGGTT | 79658 |
| rs559964395 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147953962 | ATGTTGTGTTTTTAT[G/T]TCGTTCTTTTCAGAA | 79658 |
| rs559967414 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147866425 | TGGGATTCTCCTGAC[A/T]AAAGAGGACAAATGG | 79658 |
| rs559968108 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147792983 | TCTCCACTAAAAATA[C/G]AAAAATTAGCTGGGT | 79658 |
| rs559986272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147906252 | TGTTCATAGCAGCAC[C/T]GTTCACAACAGGCAA | 79658 |
| rs560008790 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148040618 | AAGTGCTGGGATTAC[A/G]GACATGAGCTGCAGC | 79658 |
| rs560024301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147952226 | GCTAAAAGCATTTGT[A/G]TACCTATATTTGAGT | 79658 |
| rs560031402 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147884829 | CTTGAGATGGGGCAA[C/T]GGCCTGAACTTGAAG | 79658 |
| rs560037686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147910215 | TGTTGTTGAGATGGG[A/G]TCTTGCTATGTTGTC | 79658 |
| rs560049860 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148029986 | GAAACCTCCCGTGAG[C/G]CTCAGCATCCCCCCC | 79658 |
| rs560057673 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148012966 | TAAAGAGCTGTTTTG[A/T]GTTTGCCAACATTTC | 79658 |
| rs560068326 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148041839 | AGAACACTGTGTTGT[A/C]TTTAAAACAACAAAA | 79658 |
| rs560074315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147818715 | ATTGGAAAGAAAATA[C/T]ATTTAATGGACTGCA | 79658 |
| rs560075736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147915430 | CTTTGTGTCATTTGC[A/G]TGCTTATTAATTTGG | 79658 |
| rs560085482 | snp | C/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147764334 | AGGCTGGAGACCCTA[C/G]TCTGAGCTTGCCAGG | 79658 |
| rs560099080 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147741240 | TGAAATTTGTTTTAT[A/T]AATTTAGGATACTAG | 79658 |
| rs560114538 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148004396 | GATTTAAATAGTGAT[A/G]GTGATTGTGGCAGAC | 79658 |
| rs560123239 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147874783 | TTAGAAAGCCTCCAA[A/G]GTAACCTGTAGTAAC | 79658 |
| rs560126887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147786541 | CTGCAGGAGCAAAAG[A/G]GGGGAAAATTCCATG | 79658 |
| rs560128822 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148050942 | GGCTCTTAATAGGAG[C/G]CAATGCCTTTACTGT | 79658 |
| rs560136303 | snp | C/T | 0 | 0 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147826187 | GACCATTGTTAGGCT[C/T]AGTATTCTGTTTCTG | 79658 |
| rs560145597 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147899707 | AAATTAGGCAACATG[C/G]TTTTATCATCTCTGG | 79658 |
| rs560154006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147732718 | CCCCGCCTGGGCCCC[A/G]CCTGGCCCCGGCCGA | 79658 |
| rs560156142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147779627 | ATTTCCTTCAGTTTG[A/G]GAGTCTGGGGAGTGG | 79658 |
| rs560165378 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147796933 | CATAGAGCCCTTCCA[C/T]GGAGGCTTGTTGATT | 79658 |
| rs560176767 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:148060005 | GAGAGGGGAGAGAGA[C/G]GAGAGAGAGAGGGGA | 79658 |
| rs560183161 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147767108 | CACCCACTTTGGCCG[C/G]CCAAAGTGCTGGGAT | 79658 |
| rs560186636 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147747757 | TTATTTCAGCTGTCA[A/G]TGAGAGGAATCAGAC | 79658 |
| rs560186806 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147740801 | AGATACTTTAGAAAT[A/T]TAAAAAGATAGTCTC | 79658 |
| rs560188742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147992949 | GAAACTGATTGGAGG[A/G]TGTATTGAAGAAGGC | 79658 |
| rs560195142 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147773712 | CCAAAAGCCTTAAAG[G/T]GGAATGATAGGGAAT | 79658 |
| rs560198851 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147875602 | CCCTGCCTCTCTGTC[A/G]TCTTAAGGTCAAGAG | 79658 |
| rs560206886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147886316 | TGGCTTCTTGACTTG[C/T]TAAGTTCCTCTCCTT | 79658 |
| rs560217925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147993494 | AGCAAACATTAAGCT[A/G]CTATGTGAACAGGTA | 79658 |
| rs560226050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147986867 | TAGTTGGTAAGTGGG[A/G]ATTCAGACCCAGGCT | 79658 |
| rs560227558 | snp | G/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147828377 | GAGCCACCAGTTATA[G/T]AAGTTCATACGCCTC | 79658 |
| rs560241571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147843355 | CTCTCTCTCTACTGC[C/T]CCACCTGGTCATTCT | 79658 |
| rs560242408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147739838 | CCTCCCAGGTTCAAG[C/T]GATTCTCCCGCCTCA | 79658 |
| rs560246641 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147835008 | TTAGCATTGTCATTC[A/T]TCGGTTGCTATTATC | 79658 |
| rs560247132 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147909557 | AGGAAATCCCAAGAG[-/T]TTTAGATGCTCTGTG | 79658 |
| rs560251357 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147860666 | TATTTTTGAAGTCTA[-/T]TTTTTTCTTCCCAAG | 79658 |
| rs560257754 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147773337 | AGAATTTTGCTGCAT[A/C]CTATATGCCTCACGG | 79658 |
| rs560260328 | snp | A/G | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147851119 | TCTTGGAAAGAGCCA[A/G]TTATAATTTTATCCA | 79658 |
| rs560261814 | in-del | -/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147879555 | TTTTAAACCACTAGA[-/T]TTTTTTTTTTTTAAG | 79658 |
| rs560279685 | snp | C/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147901919 | AACTTTAGGGGAAAA[C/T]AAAAAGGAACTAGAG | 79658 |
| rs560297569 | snp | A/T | | | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147953725 | ATTAATTTATTTTCT[A/T]TATTTTTCTGTTTTC | 79658 |
| rs560297716 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147987400 | TATTTTTCTAGACTC[G/T]GAACGCATAGCCACT | 79658 |
| rs560299094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGAP10 | GRCh38.p7 | 4:147829419 | GTCTCAAACTCCTGA[C/T]CTCGGGTGATCCACC | 79658 |