SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs717954 | snp | A/G | 0.404907 | 0.196224 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149601466 | GAGGAACATGCTTAC[A/G]GTCACGGAATTGTTA | 389337 |
rs755858 | snp | G/T | 0.0970103 | 0.197722 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149579314 | AATCAGGAAGTCTGA[G/T]CTAGGAATCAGTCTC | 389337 |
rs921977 | snp | A/T | 0.345482 | 0.231048 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149576333 | ctttgaagtcatact[A/T]ctgaggtttcagtcc | 389337 |
rs921978 | snp | A/G | 0.335788 | 0.23482 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149576469 | ATCATCTAGCAGAAT[A/G]CCTGGCTTATAGGCT | 389337 |
rs965876 | snp | A/G | 0.427119 | 0.176434 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149614039 | cagtggctcatgctt[A/G]taatcctagcccttt | 389337 |
rs1037714 | snp | C/T | 0.493013 | 0.058691 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149573831 | atgtaaggatatcca[C/T]gttatagatatgata | 389337 |
rs1056189 | snp | A/G | 0.265453 | 0.249522 | utr-variant-3-prime | ARHGEF37 | GRCh38.p7 | 5:149634855 | GTTGTGGAGATGAGG[A/G]CAAGATTACAATATC | 389337 |
rs1056993 | snp | C/T | 0.428126 | 0.175417 | synonymous-codon | ARHGEF37 | GRCh38.p7 | 5:149628840 | CACATGGTACAGCTG[C/T]AGTTTCCCAGCCGGC | 389337 |
rs1135093 | snp | C/T | 0.423768 | 0.179735 | missense | ARHGEF37 | GRCh38.p7 | 5:149628958 | TACTCACCTGGTTCA[C/T]GGTGGGAATAGAGGG | 389337 |
rs1379544 | snp | C/T | 0.466412 | 0.125164 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149601483 | TCACGGAATTGTTAG[C/T]GATGCAGCTAAATCT | 389337 |
rs1379545 | snp | A/G | 0.493881 | 0.054972 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149613041 | TGTCAGGGTGGAAAA[A/G]GCGGCCTTGCAGAGG | 389337 |
rs1457699 | snp | C/T | 0.453453 | 0.145282 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149591362 | tttgaggattacagg[C/T]gtgagccaccgtgct | 389337 |
rs1457700 | snp | A/G | 0.473359 | 0.112298 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149591420 | atgaggtctctctct[A/G]ttgcccaggctggag | 389337 |
rs1531233 | snp | C/T | 0.432797 | 0.170544 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149588704 | GATTGTTTTCCTTTT[C/T]CCCCCCTTCCTTAAA | 389337 |
rs1531234 | snp | G/T | 0.479824 | 0.098392 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149588729 | CTTAAATGTTTAAAT[G/T]GGCTCCTCCTGGGAG | 389337 |
rs1531235 | snp | A/G | 0.406296 | 0.19512 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149588812 | TTAAAGCCTTGGGCA[A/G]CTAGCTGATGGATCC | 389337 |
rs1531236 | snp | A/G | 0.349671 | 0.229272 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149615102 | CCAGATACACCACTG[A/G]TGCATGGATGACTAG | 389337 |
rs1563625 | snp | A/G | 0.496681 | 0.0405994 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149598822 | tatgtgtgtgtgtgt[A/G]tatatatatatgtat | 389337 |
rs1563626 | snp | A/T | 0.372995 | 0.217652 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149608376 | AAATATGCAAACAAA[A/T]ttttttttttttgag | 389337 |
rs1870229 | snp | C/T | 0.471958 | 0.115042 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149599314 | GAGCCCAGCCCCTCT[C/T]CTGTGGCTGAGCAGG | 389337 |
rs1902794 | snp | C/G | 0.452473 | 0.146644 | | | GRCh38.p7 | 5:149593577 | gtagttaagtttttg[C/G]tgagtcagaagttat | 389337 |
rs1960010 | snp | A/G | 0.472429 | 0.114129 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149602257 | AGACAGGGTTTCACC[A/G]TATTGGTCAGACTTG | 389337 |
rs1960011 | snp | A/G | 0.437542 | 0.165312 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149602182 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGAGACTAC | 389337 |
rs1968762 | snp | A/G | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149588083 | tttgtattgttagta[A/G]agacagggtttcacc | 389337 |
rs1968763 | snp | A/G | 0.406296 | 0.19512 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149588186 | ACAGGCGTGAGCCAC[A/G]GTGCCCGGCCTTTTT | 389337 |
rs2125131 | snp | C/T | 0.406296 | 0.19512 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149587953 | GCTGAGATCATGCCA[C/T]TGCACTCCAGCCTGG | 389337 |
rs2125132 | snp | A/G | 0.0558544 | 0.157504 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149587927 | cctgggcgacagagt[A/G]agactttgtctccaa | 389337 |
rs2168773 | snp | G/T | 0.0558544 | 0.157504 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149588301 | taaatattttacttg[G/T]attatcttaagaaat | 389337 |
rs2168774 | snp | A/G | 0.361894 | 0.223562 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149572671 | ctttactcaaagtct[A/G]ctgatgtaaaggtta | 389337 |
rs2279019 | snp | C/T | 0.172028 | 0.23753 | utr-variant-5-prime, upstream-variant-2KB | CSNK1A1, ARHGEF37 | GRCh38.p7 | 5:149551313 | CTGGGCCGGAGCCGG[C/T]GGCAGTGGTGGCAGC | 389337 |
rs2279132 | snp | C/T | 0.2768 | 0.248559 | utr-variant-3-prime | ARHGEF37 | GRCh38.p7 | 5:149634024 | CACACAGTAGGCCTT[C/T]GGTAGGTATCTGTGG | 389337 |
rs2279133 | snp | A/G | 0.14665 | 0.227637 | utr-variant-3-prime | ARHGEF37 | GRCh38.p7 | 5:149632490 | GACTGGCCATAACCT[A/G]TGGAGAGTCCTGGCC | 389337 |
rs2279134 | snp | C/G | 0.439224 | 0.163383 | utr-variant-3-prime | ARHGEF37 | GRCh38.p7 | 5:149632488 | CTGGCCATAACCTAT[C/G]GAGAGTCCTGGCCAA | 389337 |
rs2400884 | snp | C/T | 0.406296 | 0.19512 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149587982 | GCTCAGTGCAACCTC[C/T]GCCTCCTGGGTTCAA | 389337 |
rs2400885 | snp | C/T | 0.445987 | 0.155207 | intron-variant, upstream-variant-2KB | ARHGEF37 | GRCh38.p7 | 5:149596102 | cttccttacccaccc[C/T]tctactttgggccac | 389337 |
rs2400886 | snp | A/T | 0.38286 | 0.211774 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149597267 | TTATCTATTAAAAAA[A/T]AATTTTTTTTGTAAG | 389337 |
rs2400887 | snp | A/T | 0.483563 | 0.0891524 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149597268 | TATCTATTAAAAAAA[A/T]ATTTTTTTTGTAAGA | 389337 |
rs2400888 | snp | A/T | 0.483126 | 0.0902898 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149597269 | ATCTATTAAAAAAAA[A/T]TTTTTTTTGTAAGAA | 389337 |
rs2400889 | snp | C/T | 0.44546 | 0.155869 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149598542 | GGTCTCTTTATTCGA[C/T]CACAAAGTCACTGTC | 389337 |
rs2400890 | snp | A/G | 0.497907 | 0.0322805 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149609260 | GCACTGTCCAAATGT[A/G]AGCATTATTAATATT | 389337 |
rs2400891 | snp | C/T | 0.49762 | 0.0344131 | synonymous-codon, utr-variant-5-prime | ARHGEF37 | GRCh38.p7 | 5:149609559 | TCAGGTAACATATTT[C/T]TGGAATTCCAAGAGG | 389337 |
rs2400892 | snp | C/T | 0.484066 | 0.0878235 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149616316 | ctgctgtggagaggc[C/T]gagcaagctgagggc | 389337 |
rs2895862 | snp | C/T | 0.431325 | 0.172108 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149587895 | TCCCTCCCTTTAGTC[C/T]TTTTTTTTTTTTTTT | 389337 |
rs2895863 | snp | C/T | 0.123105 | 0.215401 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149591962 | ATCAGGACATAACCT[C/T]ATTGTAAGTCGAAGA | 389337 |
rs2895864 | snp | C/T | 0.330249 | 0.23677 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149592062 | aatagcaaagggagg[C/T]cctctgtactgttca | 389337 |
rs2895865 | snp | C/T | 0.453331 | 0.145452 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149593403 | attctggtcatttca[C/T]ataaatgcaataata | 389337 |
rs2895866 | snp | A/T | 0.0532157 | 0.154195 | intron-variant, upstream-variant-2KB | ARHGEF37 | GRCh38.p7 | 5:149595354 | CTAATTACAAAAAAA[A/T]TTTTTCTGTAGAGAC | 389337 |
rs2895867 | snp | A/G | 0.471673 | 0.115589 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149598544 | TCTCTTTATTCGATC[A/G]CAAAGTCACTGTCAG | 389337 |
rs3073426 | in-del | -/AAAGA | 0.480382 | 0.097079 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149582668 | GTTCTAGCATAAAGA[-/AAAGA]CAAATATTTAAAGTG | 389337 |
rs3073427 | in-del | -/CTTG/TTTG | 0 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149588230 | TTGTTTGTTTGTTTG[-/CTTG/TTTG]CTTTGAGACAGAATC | 389337 |
rs3073428 | in-del | -/GCTT | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149588233 | TTTGTTTGTTTGCTT[-/GCTT]TGAGACAGAATCTTG | 389337 |
rs3073459 | in-del | -/CT | 0.375 | 0.216506 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149598750 | CTCatatatatatat[-/CT]atatatagatataga | 389337 |
rs3073460 | in-del | -/TA | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149598763 | atctatatatagata[-/TA]gatatagatatagat | 389337 |
rs3073461 | in-del | -/TTT | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149602072 | ttctttttttttttt[-/TTT]gagacggagtctcac | 389337 |
rs3205250 | snp | A/G | 0 | 0 | utr-variant-3-prime | ARHGEF37 | GRCh38.p7 | 5:149632660 | GCTGACTCATTGGTT[A/G]TGATGTCTCCTGATA | 389337 |
rs3205251 | snp | G/T | 0 | 0 | utr-variant-3-prime | ARHGEF37 | GRCh38.p7 | 5:149632571 | TCCTGCAACCACACA[G/T]CACGCAGGTAACATT | 389337 |
rs3733658 | snp | C/T | 0.388964 | 0.20782 | utr-variant-3-prime | ARHGEF37 | GRCh38.p7 | 5:149633219 | GCATGCTTAGCCCCA[C/T]GTCATTCTCAGCACA | 389337 |
rs3733659 | snp | A/G | 0.0601824 | 0.162694 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149628998 | CCGGATGGCCGATGG[A/G]AGGCAAGCCCCCAGC | 389337 |
rs3733661 | snp | C/T | 0.0549504 | 0.156383 | synonymous-codon | ARHGEF37 | GRCh38.p7 | 5:149628921 | AGCTGGGCTGGGCTC[C/T]GGTGTTAGACATCGG | 389337 |
rs3733662 | snp | G/T | 0.273334 | 0.248909 | missense | ARHGEF37 | GRCh38.p7 | 5:149628904 | GTGTTAGACATCGGG[G/T]GTCTTTGTTCAGCCC | 389337 |
rs3994917 | in-del | -/T | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149587913 | TTTTTTTTTTTTTTT[-/T]GGAGACAAAGTCTCA | 389337 |
rs4075280 | snp | A/C | 0.344815 | 0.231323 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149624688 | TCTGCCTTCCAGGCT[A/C]AAGCAATTCTTCTGC | 389337 |
rs4075281 | snp | A/G | 0.410737 | 0.191478 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149624553 | CTCTTGGCCTCAAGT[A/G]ATCCACCCACCTCGG | 389337 |
rs4235744 | snp | C/G | 0.470908 | 0.117046 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149622504 | CCTGTTTGGAGCACT[C/G]TCCATGCATGATCTC | 389337 |
rs4291000 | snp | A/G | 0.0524604 | 0.153226 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149624480 | TTCAAATTGTCATCA[A/G]AAGGTATCCTTGGCC | 389337 |
rs4320246 | snp | A/G/T | 0.226248 | 0.267174 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149624302 | TATTTGAGCTGGGGT[A/G/T]GGGGGACACACCCAG | 389337 |
rs4382154 | snp | A/G | 0.135484 | 0.22223 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149620780 | AGGTTGCAGTGAGCC[A/G]AGATCATGCCACCGC | 389337 |
rs4409073 | snp | A/G | 0.410737 | 0.191478 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149622387 | CTAGAAGTTGATGAC[A/G]GAGACAGAAGGTCGT | 389337 |
rs4443410 | snp | C/G | 0.450859 | 0.148847 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149571221 | ggctgggattacagg[C/G]atgagccaccgcgtc | 389337 |
rs4489048 | snp | C/T | 0.290201 | 0.246747 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149631240 | GCAGTGCCATGATCT[C/T]GGCTTACTGCAGCCT | 389337 |
rs4499821 | snp | A/C | 0.466412 | 0.125164 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149619822 | cgcctgtaatcccag[A/C]attttggaaggccga | 389337 |
rs4629585 | snp | A/C | 0.486704 | 0.080444 | missense | ARHGEF37 | GRCh38.p7 | 5:149621988 | TGGCTGGGCCAGATC[A/C]TGTGCACATTCGTGA | 389337 |
rs4705074 | snp | A/G | 0.472147 | 0.114677 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149610444 | TTTCGAATGGGTAAC[A/G]TGATTATAAGATTAA | 389337 |
rs4705075 | snp | G/T | 0.325091 | 0.238456 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149610650 | CATTTTCCCTTTTTA[G/T]TCATCCTTCATGGGT | 389337 |
rs4705076 | snp | C/G | 0.248716 | 0.249997 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149615946 | AGGCAGCAGACCATT[C/G]TATTAAATAAGATAT | 389337 |
rs4705077 | snp | A/G | 0.292211 | 0.246411 | utr-variant-3-prime | ARHGEF37 | GRCh38.p7 | 5:149633851 | TGAAGACTGCATGAC[A/G]CAAGAGAAATGCAAG | 389337 |
rs4705349 | snp | A/G | 0.33875 | 0.233717 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149557478 | TTTGTTTGTTTGTTT[A/G]TTTATTTATTTATTT | 389337 |
rs4705350 | snp | A/G | 0.474723 | 0.109542 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149559672 | CAACAATTTCCAATT[A/G]TGTTTTGATATAGTT | 389337 |
rs4705351 | snp | C/T | 0.431473 | 0.171952 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149559739 | CTTTTCATTTATCTT[C/T]ACAGACTTAAAAGAG | 389337 |
rs4705352 | snp | C/T | 0.407502 | 0.194147 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149569912 | aggtgtgagccactg[C/T]acctgaccAtatgtt | 389337 |
rs4705353 | snp | A/G | 0.400325 | 0.199756 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149585334 | ttgtaatagtgaaac[A/G]ggaaacaaacagttg | 389337 |
rs4705354 | snp | A/T | 0.480302 | 0.0972668 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149585662 | agctgggattacagg[A/T]gtctgccaccacgcc | 389337 |
rs4705355 | snp | A/C | 0.480302 | 0.0972668 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149585665 | tgggattacaggtgt[A/C]tgccaccacgcccag | 389337 |
rs4705356 | snp | C/T | 0.480302 | 0.0972668 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149585674 | aggtgtctgccacca[C/T]gcccagctaattttt | 389337 |
rs4705357 | snp | A/C | 0.472429 | 0.114129 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149604438 | CTCTCTCCCCTGCAA[A/C]TTTGGCAGTCCTGTT | 389337 |
rs4705358 | snp | C/T | 0.434398 | 0.168811 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149604785 | CCTCCTGGGTTCAAG[C/T]GATTCTCATGTCTCA | 389337 |
rs5872137 | in-del | -/TTGC | 0.40386 | 0.197046 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149588227 | TGTTTGTTTGTTTGT[-/TTGC]TTGCTTTGAGACAGA | 389337 |
rs5872138 | in-del | -/T | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149613765 | TTCTACAGTGTTTTC[-/T]TTTTTTTTTTTTTTT | 389337 |
rs5872139 | in-del | -/TATAA/TGTAA | 0.436643 | 0.173512 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149624649 | GTGGTGGTGTGCACC[-/TATAA/TGTAA]TCCCAGCTACTTGGG | 389337 |
rs5872140 | in-del | -/GTAAT | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149624650 | TGGTGGTGTGCACCT[-/GTAAT]CCCAGCTACTTGGGA | 389337 |
rs6149294 | in-del | -/ATAATAAATATATTACATATGTAATATGACATAT | 0 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149608305 | TGTAATATGACATAT[lengthTooLong]GAGGATGGCGATTAA | 389337 |
rs6579743 | snp | G/T | 0.32955 | 0.237006 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149591063 | gaggacctctttTAG[G/T]tctttttttcttttt | 389337 |
rs6579744 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149600097 | TATTGCTCCTAGGCT[A/G]TAAGTGTGTTCAGCA | 389337 |
rs6579745 | snp | C/T | 0.324619 | 0.238604 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149600585 | CCCCGGTTCAGCTTT[C/T]CTTCCCCACTGAGTA | 389337 |
rs6579746 | snp | C/G | 0.324619 | 0.238604 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149606813 | agttgcttcctgcaa[C/G]catcagaataaaacc | 389337 |
rs6579747 | snp | A/G | 0.407674 | 0.194008 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149606980 | gagtgcagtggtgca[A/G]tctcagctcactgct | 389337 |
rs6579748 | snp | G/T | 0.471388 | 0.116136 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149611927 | taatggcttcactaa[G/T]aaaggagaaataaaa | 389337 |
rs6579749 | snp | A/G | 0.150333 | 0.229274 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149617628 | CATCACTTGCTTCCT[A/G]TCGCAGAACTGGTAA | 389337 |
rs6579750 | snp | A/G | 0.150333 | 0.229274 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149618123 | ATGTCCGTGACATCC[A/G]CTTTCCTGAGTTGGC | 389337 |
rs6859243 | snp | C/G | 0.49827 | 0.0293608 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149590934 | ACACTTAATAAAATA[C/G]AATAGAACAATCAAA | 389337 |
rs6861325 | snp | C/T | 0.0422008 | 0.138995 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149629958 | aaggccacataggat[C/T]ccattatgtggatgt | 389337 |
rs6861618 | snp | C/T | 0.405776 | 0.195535 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149579090 | GAGTGTTGACACTTA[C/T]GTCTAAAACCACAGA | 389337 |
rs6867171 | snp | G/T | 0.344147 | 0.231595 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149587043 | AATGAACTATTTGTT[G/T]TAATCAAGTGGCAGA | 389337 |
rs6867642 | snp | A/G | 0.469839 | 0.119042 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149610178 | CAGGGTTGGAGAAGC[A/G]GAAACGTTTGGGAAC | 389337 |
rs6869554 | snp | A/G | 0.414741 | 0.188044 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149628186 | ACCACTTTGCTGACT[A/G]TGTGATCTCAGGGAA | 389337 |
rs6869628 | snp | A/G | 0.473451 | 0.112115 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149628439 | CAGTCTCCGCCTCCT[A/G]GGAAAGGCAGTCCTG | 389337 |
rs6869644 | snp | C/T | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149589107 | ggtggcacatgtctg[C/T]agtcccagctatgtg | 389337 |
rs6869753 | snp | C/G | 0.484771 | 0.0859212 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149628403 | CATAAAGGAACTGGG[C/G]TCACATGGAGAGGAG | 389337 |
rs6873616 | snp | G/T | 0.14933 | 0.228835 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149611307 | aataatagcagtgat[G/T]tttttgcaaaccatc | 389337 |
rs6874995 | snp | C/G | 0.407971 | 0.193766 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149629188 | ACAAAGAACTAACCC[C/G]TTGTTCCTCATCAGC | 389337 |
rs6879304 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149612424 | cgcccacctcggcct[C/T]ccagagtgctgggat | 389337 |
rs6880432 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149590772 | cggctaatttttttg[C/T]attttttatagagat | 389337 |
rs6880916 | snp | A/C | 0 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149570161 | aatcatgaattttta[A/C]aacacctactaaagc | 389337 |
rs6881958 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149587575 | tccagggcctgggct[C/T]ctaaccTTCACCACA | 389337 |
rs6882002 | snp | A/G | 0.404209 | 0.196773 | intron-variant, upstream-variant-2KB | ARHGEF37 | GRCh38.p7 | 5:149594698 | CAGGAAAATGAGCAC[A/G]CTGAGCACAAGGTTA | 389337 |
rs6884631 | snp | A/T | 0.287606 | 0.247155 | utr-variant-3-prime | ARHGEF37 | GRCh38.p7 | 5:149634281 | TGCCAGAGATGGCCA[A/T]GAGCTGTAAGCTAGG | 389337 |
rs6888407 | snp | A/G | 0.432797 | 0.170544 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149589128 | cagctatgtgggagg[A/G]ttgcttgagcccagg | 389337 |
rs6889482 | snp | C/T | 0.0973687 | 0.197999 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149574554 | tcgtgcatttactgc[C/T]ttcctagagtgatct | 389337 |
rs6893973 | snp | A/G | 0.403158 | 0.197592 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149596941 | AGCAGGGCACACCAT[A/G]TTCACAAGCTTTGTT | 389337 |
rs6894391 | snp | C/T | 0.484701 | 0.0861117 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149627496 | TCGTTGCAGGGTCTA[C/T]CATGAAGCACCTATG | 389337 |
rs6899005 | snp | C/G | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149590569 | acaggtgtgagccac[C/G]gcgtctggccTGGCT | 389337 |
rs7443869 | snp | A/G | 0.472335 | 0.114312 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149609749 | CTGACCCGGTTCAGG[A/G]GCAGCTATGGTCTCA | 389337 |
rs7447560 | snp | C/T | 0.472335 | 0.114312 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149609757 | GTTCAGGAGCAGCTA[C/T]GGTCTCACCCCTTTT | 389337 |
rs7448026 | snp | C/T | 0.370775 | 0.218891 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149598266 | TGCTTAAACTGACTC[C/T]TCTTCTTCTTCTTCT | 389337 |
rs7449103 | snp | G/T | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149623675 | CCTGCCTTATCTGTG[G/T]CCTGTGGTCCATGCA | 389337 |
rs7700256 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149560711 | agatgacttgagctt[A/G]ggagtttgagaccag | 389337 |
rs7700512 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149560688 | aacactttggagggc[A/G]agggggcagatgact | 389337 |
rs7701251 | snp | A/C | 0.0912534 | 0.193131 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149621449 | tctcaaaaaaaaaaa[A/C]aaaaaaCTTTTTCAA | 389337 |
rs7701988 | snp | A/G | 0.398174 | 0.201356 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149608560 | gtatttttagtaaag[A/G]cagggttttaccatg | 389337 |
rs7705454 | snp | A/G | 0.332869 | 0.238352 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149591742 | ctatttttcactttc[A/G]atactgtattcaatt | 389337 |
rs7706777 | snp | C/T | 0.432504 | 0.170857 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149586530 | ggcctcccgaagtgc[C/T]gggattacaggtgtg | 389337 |
rs7707073 | snp | A/G | 0.338296 | 0.233889 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149586531 | gcctcccgaagtgcc[A/G]ggattacaggtgtga | 389337 |
rs7707438 | snp | A/G | 0.313003 | 0.279891 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149609847 | AGGGCAGGCTGTGCC[A/G]CAGAGACAAACAGCT | 389337 |
rs7709875 | snp | C/T | 0.471863 | 0.115225 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149598050 | CTGGGGCAAGCTTGA[C/T]AGAAAGGAAGCGTGG | 389337 |
rs7710214 | snp | C/T | 0.453697 | 0.14494 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149568143 | ctcccacctcaggct[C/T]ctgagtagctgggac | 389337 |
rs7710341 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149598188 | GGCTAACTGGTGAGC[A/G]GAATAATCACTGGGA | 389337 |
rs7710373 | snp | C/G | 0.418974 | 0.184249 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149568253 | gttggtcttgaactc[C/G]tgtgctcaaagagta | 389337 |
rs7711287 | snp | C/G/T | 0.0368353 | 0.130617 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149623008 | TTCCCCACCCCATCA[C/G/T]CTTTCTAGCCCACAG | 389337 |
rs7715047 | snp | C/T | 0.324619 | 0.238604 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149606228 | ATCTCTTAGCCAGGC[C/T]GTCTCTGCAGTTGGC | 389337 |
rs7718394 | snp | G/T | 0.405603 | 0.195673 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149581750 | TGCGACGACCTCCCG[G/T]GTCCCAACTTGCTTG | 389337 |
rs7719096 | snp | C/G | 0.432357 | 0.171014 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149582333 | AATGCCTGCAGGCTG[C/G]TACTCAGGCAGGGTG | 389337 |
rs7719197 | snp | A/G | 0.432651 | 0.170701 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149582215 | GGTTCTTAACCTTCT[A/G]GGGGTCCCTGACCCC | 389337 |
rs7721645 | snp | A/T | 0.324855 | 0.23853 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149608537 | accatcacacccggc[A/T]aatttttgtattttt | 389337 |
rs7721756 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149587689 | CAGTCTTAAAATATG[C/G]TTGGTAGTGATAGTA | 389337 |
rs7724654 | snp | A/G | 0.432504 | 0.170857 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149583230 | CAACCTCCGCCTCCC[A/G]GGTTCAAGCAATTCT | 389337 |
rs7725405 | snp | A/G | 0.329783 | 0.236927 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149600889 | TGATCCACCCGCCTC[A/G]TCTCCCCAACGTGCT | 389337 |
rs7727614 | snp | A/G | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149558693 | AAACCATATATATAt[A/G]tgtgtgtgtgtgtgt | 389337 |
rs7728256 | snp | A/G | 0.216349 | 0.247725 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149619284 | CAAAATTCACTGGAA[A/G]CAGAGCCCCGCAGAG | 389337 |
rs7731610 | snp | G/T | 0.329084 | 0.237162 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149593148 | atattctataatatt[G/T]tttTGGtagcagctt | 389337 |
rs7732029 | snp | C/T | 0.422315 | 0.181128 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149596594 | acaggcgtgagccac[C/T]gcacccggGCCCTTG | 389337 |
rs7732229 | snp | A/G | 0.224116 | 0.248656 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149626883 | TTAGAAGTTTCTTCC[A/G]AAACGCCGTAGGCTG | 389337 |
rs7732601 | snp | A/G | 0.224412 | 0.248687 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149626845 | TTCAGAACTTGAATT[A/G]GAATTTTAGAGAATC | 389337 |
rs7732714 | snp | A/C | 0.172367 | 0.237641 | missense | ARHGEF37 | GRCh38.p7 | 5:149627163 | GTGACAAGCAACATC[A/C]GTGGGACTGGGACTC | 389337 |
rs7732873 | snp | A/G | 0.44775 | 0.152954 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149627274 | GTGGACACCGGGGGT[A/G]CGTGAGCCTTTGGGA | 389337 |
rs7732874 | snp | A/G | 0.17497 | 0.238475 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149627279 | CACCGGGGGTACGTG[A/G]GCCTTTGGGAGCCCT | 389337 |
rs7733002 | snp | A/G | 0.447875 | 0.152792 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149627316 | CCTTCGGGGAAAACC[A/G]CCCCACAGAAGCCGG | 389337 |
rs7733092 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149620171 | gaaagatgttgactc[A/G]gtctaaggcggaact | 389337 |
rs7733751 | snp | A/G | 0.254664 | 0.249956 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149597408 | GGACTACAGGAGCCC[A/G]CCACCATGCCTGGCT | 389337 |
rs7733761 | snp | C/T | 0.483497 | 0.0893272 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149620476 | ATTTGTGAGTGGAAC[C/T]TTTCCTTTCTCCTTT | 389337 |
rs7737611 | snp | A/G | 0.466412 | 0.125164 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149620692 | gaaaattagccgggc[A/G]tggcagtgtgcacct | 389337 |
rs7738010 | snp | A/G | 0.492087 | 0.0623997 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149620688 | tacagaaaattagcc[A/G]ggcatggcagtgtgc | 389337 |
rs9324622 | snp | C/T | 0.43309 | 0.17023 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149626211 | ACACCCAGCACCTCC[C/T]CACAAGGAGTAACCA | 389337 |
rs9324623 | snp | C/G | 0.490782 | 0.0672626 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149626772 | CTGTGGGATAACTTA[C/G]CCTGACGGTATGGGC | 389337 |
rs9324624 | snp | C/T | 0.486966 | 0.079668 | missense | ARHGEF37 | GRCh38.p7 | 5:149627077 | TCCTCCTCTCCCAGC[C/T]GCTCCTTCCAGGGTC | 389337 |
rs9637874 | snp | A/C | 0.336245 | 0.234652 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149564035 | TTGGCTCACTGCAGC[A/C]TTCGCCTCCTGGATT | 389337 |
rs9637875 | snp | A/C | 0.43221 | 0.171171 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149586001 | CCCATGTCTTTCatt[A/C]attaattcaattaat | 389337 |
rs9885362 | snp | C/T | 0.311123 | 0.242413 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149627646 | ACGGAGATAGAATGC[C/T]TGGACCCTGGCTACA | 389337 |
rs9885369 | snp | A/C | 0.436123 | 0.166908 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149628109 | ACTTAAGGTGGGAAC[A/C]ACAGAACGGGTATTA | 389337 |
rs9885442 | snp | A/C | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149599530 | gatcctcccatctca[A/C]cctccgaagtcagcc | 389337 |
rs10037341 | snp | A/C | 0.430285 | 0.173197 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149624288 | TTCTCTCTCCTTTCT[A/C]TTTGAGCTGGGGTGG | 389337 |
rs10039565 | snp | A/G | 0.468949 | 0.12067 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149626863 | ATTTTAGAGAATCCC[A/G]GAAATTAGAAGTTTC | 389337 |
rs10040164 | snp | A/G | 0.324382 | 0.238678 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149603051 | GATTCTCCTGCCTCA[A/G]CCTCCTGAGTAGCTG | 389337 |
rs10045699 | snp | A/G | 0.19334 | 0.243495 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149602721 | CTCATCCCATCTGCT[A/G]CCAGGATTCCCATGG | 389337 |
rs10051449 | snp | C/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | ARHGEF37 | GRCh38.p7 | 5:149634150 | gattctgatgaaatt[C/G]gtttagggtgtggct | 389337 |
rs10059538 | snp | A/G | 0.442113 | 0.159977 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149613403 | TCAGGCTGGAGTGCA[A/G]TGGTGCAATCTCAGC | 389337 |
rs10061018 | snp | C/T | 0.281049 | 0.248064 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149613507 | GTGCGCCACCACGCC[C/T]GGCTAATTTTTGTAT | 389337 |
rs10065102 | snp | C/T | 0.39214 | 0.205661 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149591160 | ctctgtggtctcaac[C/T]tcctgggctcaaaac | 389337 |
rs10065458 | snp | A/G | 0.284209 | 0.247648 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149615616 | ATTTTTTTTggtcgg[A/G]tgtggtggctcacac | 389337 |
rs10068134 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149617463 | CTCAATTACATGACT[C/G]AGACAACATAAAAAT | 389337 |
rs10069731 | snp | G/T | 0.45762 | 0.139261 | upstream-variant-2KB, intron-variant | CSNK1A1, ARHGEF37 | GRCh38.p7 | 5:149552605 | CACTTCGGGAGGCCG[G/T]GGCGGGCAGATCACT | 389337 |
rs10073329 | snp | C/T | 0.292008 | 0.246445 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149615792 | agctactcgggaggc[C/T]gaggcaggagaacca | 389337 |
rs10075357 | snp | C/T | 0.192401 | 0.243274 | intron-variant, upstream-variant-2KB | ARHGEF37 | GRCh38.p7 | 5:149595800 | TTTGGGCCACCTGGA[C/T]CACATGTGTAGCATT | 389337 |
rs10075658 | snp | C/T | 0.0248432 | 0.108648 | upstream-variant-2KB, intron-variant | CSNK1A1, ARHGEF37 | GRCh38.p7 | 5:149552201 | GTGAAAAAACTGTTA[C/T]GTCCCCTCAACCCCA | 389337 |
rs10440725 | snp | A/C | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149590323 | gtctcactctgttgc[A/C]caggctggagtgcag | 389337 |
rs10463287 | snp | A/G | 0.119281 | 0.213102 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149575592 | tcttgaaaagacaca[A/G]agtagagatggccct | 389337 |
rs10463288 | snp | A/G | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149575845 | gctcagggagtttga[A/G]actagcctgggcaac | 389337 |
rs10463289 | snp | A/G | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149575933 | ttggcacCTGGCTAA[A/G]TGGTGGTTTTCAATA | 389337 |
rs10463290 | snp | C/T | 0.345037 | 0.231231 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149577768 | CTGGCTGCCCAGCCT[C/T]CATGTTACCATTATA | 389337 |
rs10476741 | snp | G/T | 0.310878 | 0.242475 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149624938 | GAGTTTCACACTGTC[G/T]CCCAGGGTGGAGTGC | 389337 |
rs10476742 | snp | A/G | 0.28052 | 0.24813 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149625185 | GTTGGAATTACAGGC[A/G]TGAGCCACCACACCT | 389337 |
rs10476743 | snp | A/C | 0.434529 | 0.174283 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149625264 | GAGGTTATCTGTTCT[A/C]GTCACTTGTAAAGTG | 389337 |
rs10476911 | snp | C/T | 0.337614 | 0.234145 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149577041 | AATACACTTTTTACA[C/T]GGTTATAGAGATCTT | 389337 |
rs10476912 | snp | C/T | 0.33693 | 0.2344 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149577066 | GATCTTTGCAGAAAG[C/T]AACCACACGAGAAAC | 389337 |
rs10476913 | snp | A/G | 0.160609 | 0.233472 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149577164 | TTACTTAATCTTTCT[A/G]AGCCTCAATTTCATC | 389337 |
rs10476914 | snp | C/T | 0.397247 | 0.224453 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149625135 | ACTCCTGCCCTCTGA[C/T]CTCAAGTGATCCACC | 389337 |
rs10515630 | snp | C/T | 0.0637235 | 0.166737 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149597670 | AAGATGTTTTTAGGC[C/T]TCTTGATGAGTAATT | 389337 |
rs10716197 | in-del | -/A | 0.42357 | 0.179927 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149620073 | GTGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAG | 389337 |
rs11167471 | snp | A/G | 0.349233 | 0.229462 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149589420 | gtagcctcaacttcc[A/G]gagttcaagcgatct | 389337 |
rs11167472 | snp | A/G | 0.472429 | 0.114129 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149606436 | CACCTCTGGCCACCA[A/G]CTGATGTGTCCCAAC | 389337 |
rs11167473 | snp | C/T | 0.325091 | 0.238456 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149607890 | tcctgcctcagcctc[C/T]cgagtagctgggact | 389337 |
rs11334969 | in-del | -/A | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149561273 | GCAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 389337 |
rs11349933 | in-del | -/T | 0.396182 | 0.202807 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149555472 | ACCATGCCTGGCTAA[-/T]TTTTTTTTTTTTTTT | 389337 |
rs11351729 | in-del | -/T | 0.480618 | 0.0965156 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149585685 | ACCACGCCCAGCTAA[-/T]TTTTTGTATTTTTAG | 389337 |
rs11390358 | in-del | -/T | 0.337841 | 0.23406 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149612177 | CTTTCTCTTTTTTTT[-/T]GAGATGGAGTCTCGC | 389337 |
rs11409449 | in-del | -/C | 0.484621 | 0.0863307 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149620318 | GATGGCCATGACAGG[-/C]CATGATTGGATGTTT | 389337 |
rs11411776 | in-del | -/T/TT | 0.498459 | 0.0277128 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149600644 | ATTTTTTTTTTTTTT[-/T/TT]GAGATGGAGTCTCGC | 389337 |
rs11478467 | in-del | -/A | 0.422315 | 0.181128 | intron-variant, upstream-variant-2KB | CSNK1A1, ARHGEF37 | GRCh38.p7 | 5:149550514 | GTAGAATTAAGAATT[-/A]AAAAAAAAAAAACAT | 389337 |
rs11556830 | snp | C/G | 0.00438332 | 0.0466095 | utr-variant-5-prime, upstream-variant-2KB | CSNK1A1, ARHGEF37 | GRCh38.p7 | 5:149551097 | TCTGGGCCCCGAACC[C/G]CGGTAAAGGCCTCCG | 389337 |
rs11556831 | snp | C/G | 0.0236746 | 0.106192 | utr-variant-5-prime, upstream-variant-2KB | CSNK1A1, ARHGEF37 | GRCh38.p7 | 5:149551281 | GTATCGCCGCCCTAG[C/G]TCACCGCGCCCCTTT | 389337 |
rs11739697 | snp | A/C | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149593209 | gcccatttaaagtgt[A/C]caaatcaatagtttc | 389337 |
rs11740185 | snp | A/C | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149605792 | tgaggctcagagagg[A/C]taagtaacattccca | 389337 |
rs11741528 | snp | A/G | 0.430434 | 0.173042 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149625434 | GCCCTGAGATTCCCC[A/G]GAGGGAGAATGGGGC | 389337 |
rs11746332 | snp | A/G | 0 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149563455 | ATGATTTGTGGCTTA[A/G]GATTTCAAGTTCTGT | 389337 |
rs11948608 | snp | A/T | 0.106278 | 0.204558 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149591831 | gggcaactgtaggct[A/T]atctaagtgttctaa | 389337 |
rs11949432 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149568416 | cctaattaaaattca[A/T]tatttatttataatg | 389337 |
rs11949439 | snp | G/T | 0.0984431 | 0.198823 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149575482 | tcttcatccctctag[G/T]ccagtgattggttta | 389337 |
rs11950259 | snp | A/G | 0.0584853 | 0.160693 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149629281 | TACTAGATGAGAGAT[A/G]CAATGATGAGCAAAA | 389337 |
rs11951544 | snp | G/T | 0.0988009 | 0.199095 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149579163 | TATTCCATCACGTAC[G/T]TCTGAAAAAAAGCGC | 389337 |
rs11951547 | snp | A/G | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149588109 | tcaccatgttggtca[A/G]gctggtcctgaactc | 389337 |
rs11954602 | snp | C/G/T | 0.0249166 | 0.109298 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149577190 | tcatcatctgtaaga[C/G/T]gcaaataatatctat | 389337 |
rs11956913 | snp | A/G | 0.411223 | 0.191068 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149629458 | GTTTTGCTGAGAAGA[A/G]TGGTGCTTTTTCTCA | 389337 |
rs11958474 | snp | C/G | 0.156319 | 0.231784 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149630615 | CCCACCAGAGCCCCA[C/G]GGGAGGGCCTGACCA | 389337 |
rs11958967 | snp | C/G | 0.209997 | 0.246779 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149626473 | TGCCACCGAATCATT[C/G]TTTCCAGCTAGATGG | 389337 |
rs11959620 | snp | C/T | 0.148996 | 0.228688 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149602205 | gagactacaagcgtg[C/T]gccaccatgcctggt | 389337 |
rs12054957 | snp | A/G | 0.409212 | 0.192748 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149589853 | TTTTTTTTTAATAGA[A/G]ATGGGGTCTCACTGT | 389337 |
rs12188428 | snp | A/G | 0.203882 | 0.245709 | upstream-variant-2KB, intron-variant | CSNK1A1, ARHGEF37 | GRCh38.p7 | 5:149553327 | ATCGCTTGAACCTGG[A/G]AGGCAGAGGTTACAG | 389337 |
rs12515482 | snp | G/T | 0.432504 | 0.170857 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149577729 | TATTAGAAGATGACT[G/T]CCATGTGGACATTTG | 389337 |
rs12515778 | snp | C/T | 0.420892 | 0.182472 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149612292 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 389337 |
rs12516409 | snp | G/T | 0.412416 | 0.190055 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149603692 | TATAATCCCAGCACT[G/T]TGGGAAGCTAAGGTG | 389337 |
rs12518478 | snp | A/G | 0.430583 | 0.172886 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149621379 | TGACAGGTAGGCTGC[A/G]GTGAGCTGTGATTGC | 389337 |
rs12522108 | snp | A/G | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149626288 | CACACACACACACAC[A/G]CCTCTCTCAAGACAT | 389337 |
rs12653732 | snp | C/G | 0.452473 | 0.146644 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149606681 | TGTCATTTTTGCAGA[C/G]GCGCCATGCTAATCT | 389337 |
rs12657287 | snp | A/G | 0.108402 | 0.206034 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149628510 | GGCATGGGAGCTGGC[A/G]GCTCCATCAGATAAG | 389337 |
rs13155938 | snp | G/T | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149557962 | cctctgtctcctggg[G/T]tcaagcaattctcct | 389337 |
rs13155951 | snp | G/T | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149557994 | cctctgcctcccaag[G/T]agctgggattacagg | 389337 |
rs13160485 | snp | A/C | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149605056 | acatagtgaaacccc[A/C]cctctactaaaaata | 389337 |
rs13160938 | snp | A/G | 0.471768 | 0.115407 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149605301 | ttttcaagtagctac[A/G]ttaagaaaattaaag | 389337 |
rs13161523 | snp | C/T | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149598357 | ttcctcttcttcttc[C/T]tcttcctcttcttcc | 389337 |
rs13161661 | snp | C/T | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149598408 | ctctccttcctcttc[C/T]tcttctccttcttct | 389337 |
rs13171496 | snp | A/C | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149607128 | ggctggtctcaaact[A/C]ctggcctcaagtgat | 389337 |
rs13172354 | snp | A/G | 0.338976 | 0.23363 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149570469 | taatcacagctactc[A/G]ggaggttgaggcagg | 389337 |
rs13173926 | snp | C/G | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149557996 | tctgcctcccaagta[C/G]ctgggattacaggtg | 389337 |
rs13178484 | snp | G/T | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149586792 | tagtccttattactg[G/T]cctgtctctgccctc | 389337 |
rs13179038 | snp | A/G | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149558735 | tgtgtgtgtgtgtgt[A/G]tgtatatatattttt | 389337 |
rs13179497 | snp | A/G | 0.408871 | 0.193029 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149559092 | ctttgggaggccgag[A/G]tgggcagatcatgag | 389337 |
rs13179527 | snp | G/T | 0.00454543 | 0.0474558 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149555584 | cctcccaaaacgcta[G/T]gatgacaggcaagaa | 389337 |
rs13181638 | snp | C/T | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149598351 | TTCCTCTTCCTCTTC[C/T]TCTTCCTCTTCCTCT | 389337 |
rs13181653 | snp | C/T | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149598384 | ttcctcttcctcttc[C/T]tcctcttcctctcct | 389337 |
rs13181783 | snp | C/T | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149598417 | ctcttcctcttctcc[C/T]tcttctccttctcct | 389337 |
rs13184089 | snp | C/T | 0.340333 | 0.233109 | upstream-variant-2KB, intron-variant | CSNK1A1, ARHGEF37 | GRCh38.p7 | 5:149553005 | AAGCCCAACCAACAC[C/T]CAGGGTGCCCAACTC | 389337 |
rs13184845 | snp | C/T | 0.32885 | 0.23724 | upstream-variant-2KB, intron-variant | ARHGEF37 | GRCh38.p7 | 5:149581123 | CACTAAGAATTAAAT[C/T]GAGGCCCAGCCCTAC | 389337 |
rs13361215 | snp | G/T | 0.0228947 | 0.104514 | intron-variant, upstream-variant-2KB | ARHGEF37 | GRCh38.p7 | 5:149595739 | acattttattttgtt[G/T]tggccactcagaatt | 389337 |
rs17654288 | snp | C/T | 0.184838 | 0.241358 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149609795 | ATTCGTGCTGCTTCA[C/T]GAGTGTTGCTCTGTC | 389337 |
rs17724261 | snp | A/G | 0.280785 | 0.248097 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149628459 | AGGCAGTCCTGGGGA[A/G]AGGAAGCAGCTCTTG | 389337 |
rs28406004 | snp | A/G | 0.371582 | 0.218444 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149618687 | AAACAGAAACTCCGA[A/G]AGGGTAAAACCCTTG | 389337 |
rs28444959 | snp | C/T | 0.337614 | 0.234145 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149584017 | CTCCCACCTCAGCCT[C/T]CCAAAGTGCTGGGAT | 389337 |
rs28445711 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149604844 | TGCGCCACCACGCCC[A/G]GCTAATTTTTGTATT | 389337 |
rs28469375 | snp | A/G | 0.371987 | 0.218218 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149618685 | GAAAACAGAAACTCC[A/G]AGAGGGTAAAACCCT | 389337 |
rs28547951 | snp | C/T | 0.288646 | 0.246995 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149621378 | CTGACAGGTAGGCTG[C/T]GGTGAGCTGTGATTG | 389337 |
rs33975902 | in-del | -/AAAGT | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149586239 | TTCAAGCAGAGAAGT[-/AAAGT]GACAAATTTTATGTT | 389337 |
rs34062323 | in-del | -/G | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149599965 | CACTTAACACCAGGG[-/G]ATATGTTTTGAGGAA | 389337 |
rs34084231 | in-del | -/T | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149590594 | CTTTTTTTTTTTTTT[-/T]GAGGCAGAATTTCAC | 389337 |
rs34088372 | in-del | -/GAGA | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149584372 | TCCAGGAAAGAGAGA[-/GAGA]ATGTGTATGTCTGTC | 389337 |
rs34107862 | in-del | -/TTTA | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149556400 | TTATTTATTTATTTA[-/TTTA]TTTTGAGATGGAGTC | 389337 |
rs34166602 | in-del | -/TTCA | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149629245 | TCATTCATTCATTCA[-/TTCA]ATATTTGCCAGGCAC | 389337 |
rs34220379 | in-del | -/C | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149598750 | CTCATATATATATAT[-/C]TATATATAGATATAG | 389337 |
rs34322237 | in-del | -/T | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149613349 | TTTTTTTTTTTTTTT[-/T]GAGACGGAGTTTTGC | 389337 |
rs34336983 | in-del | -/T | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149629835 | CAACGCGAGCTCTTT[-/T]GTACAATGGAATATT | 389337 |
rs34343291 | in-del | -/T | 0.372592 | 0.217879 | intron-variant, upstream-variant-2KB | ARHGEF37 | GRCh38.p7 | 5:149595946 | GTGTGGATAGCTGCA[-/T]TTTTTTTTTTTTTTC | 389337 |
rs34356323 | in-del | -/A | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149617189 | CTGATTGGCTTAGGT[-/A]CTGGGTTATGTGCCC | 389337 |
rs34363940 | in-del | -/A | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | CSNK1A1, ARHGEF37 | GRCh38.p7 | 5:149550526 | ATTAAAAAAAAAAAA[-/A]CATGGGAATCACTGA | 389337 |
rs34397621 | snp | A/G | 0.0941369 | 0.195465 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149561443 | GACTTTTACTCTTCA[A/G]CGTAGTCTAATCCTT | 389337 |
rs34471125 | in-del | -/A | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149589809 | AGGTGTGAGCCACCA[-/A]TGCCCGGCCGCCTGG | 389337 |
rs34525755 | in-del | -/T | 0 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149587902 | TTTTTTTTTTTTTTT[-/T]GGAGACAAAGTCTCA | 389337 |
rs34559689 | in-del | -/T | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149626160 | GCAGAGTCTGTGGCC[-/T]AAATGTTCCTGAAGG | 389337 |
rs34564721 | in-del | -/G | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149563132 | GCTGTCTGATCCCGG[-/G]TTACTCACCTCTGTC | 389337 |
rs34594110 | snp | A/G | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149568745 | GGCACCTGGGAGGCA[A/G]AGGTTGCAGTGACCT | 389337 |
rs34647122 | in-del | -/A | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149592677 | TGAGTTACACAGAAA[-/A]GTGTATGTTTTATTT | 389337 |
rs34686189 | in-del | -/A | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149596791 | TGCAAGTATGGAGAA[-/A]GAGCGCTCAACTCTC | 389337 |
rs34737789 | in-del | -/C | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149577751 | GACATTTGTCATTTT[-/C]CCTGGCTGCCCAGCC | 389337 |
rs34784339 | in-del | -/C | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149561024 | CACGCCTGTAATCCC[-/C]AGCACTTTGGGAGGC | 389337 |
rs34811230 | in-del | -/C | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149571996 | CCAAAACAACCCTGG[-/C]AAAATAAGAACAAAC | 389337 |
rs34816076 | in-del | -/T | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149593727 | TTATTTAAAAAATCA[-/T]GGAGAAGAGAAAAAA | 389337 |
rs34821745 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149615787 | ATCCCAGCTACTCGG[A/G]AGGCTGAGGCAGGAG | 389337 |
rs34861230 | in-del | -/C | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149616938 | CTGGCTCCAGTTCCC[-/C]TGTAACTCCCTTGTC | 389337 |
rs34862330 | in-del | -/C | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149587850 | GGTAGCCAGGGTCCC[-/C]TATGTGCACATTCTT | 389337 |
rs34871504 | in-del | -/G | 0 | 0 | intron-variant, upstream-variant-2KB | ARHGEF37 | GRCh38.p7 | 5:149595995 | TTGTGGCTGGGGGGG[-/G]TCCCAGTTCTGTGAA | 389337 |
rs34943811 | snp | A/C | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149615555 | TTTTTACCCCTAAAT[A/C]CTTTAAATAAATCTC | 389337 |
rs34953047 | snp | C/T | 0.432504 | 0.170857 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149577538 | GATTAAAAAAAATGG[C/T]ATGGGAAGAAAGTAT | 389337 |
rs35015798 | in-del | -/C | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149585609 | GCAACCTCCGCCTCC[-/C]TGGGTTCTAGCGAGT | 389337 |
rs35020736 | snp | C/T | 0.430434 | 0.173042 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149560230 | AAGTGATTCACCTGC[C/T]TCAGCCTCCCAAGTA | 389337 |
rs35071982 | in-del | -/T | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149593727 | TATTTAAAAAATCAT[-/T]GGAGAAGAGAAAAAA | 389337 |
rs35095261 | in-del | -/G | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149631008 | CAATGTCCTGAAGGG[-/G]ATGGGACCATTCCCT | 389337 |
rs35217743 | in-del | -/T | 0.43978 | 0.162738 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149614123 | TTAGACTATGGTTTA[-/T]TTGGCCATTCCTCTA | 389337 |
rs35237101 | snp | A/G | 0.030665 | 0.119967 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149592396 | ATGGAATCACACAGT[A/G]TGTGACCTTTAAAGA | 389337 |
rs35255200 | snp | A/G | 0.107694 | 0.205546 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149628485 | TCTTGCTCTGGGCAG[A/G]CACCAGAGGGGCATG | 389337 |
rs35298658 | in-del | -/T | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149561667 | CTGCATTTCGCCTGT[-/T]GTTTCCTATCCCACT | 389337 |
rs35332196 | in-del | -/G | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149557651 | CCTGGCCTAACAGGG[-/G]AGTTGCTTTAGCCTC | 389337 |
rs35336600 | snp | A/G | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149559649 | CTTAAAATTCCTTGT[A/G]TCATAAACAACAATT | 389337 |
rs35342997 | in-del | -/G | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149617780 | TGAGTCAGGACCGGG[-/G]AAGCGTGGCTCCCAG | 389337 |
rs35436322 | snp | C/G | 0.433236 | 0.170072 | utr-variant-5-prime, intron-variant | ARHGEF37 | GRCh38.p7 | 5:149581578 | GCGCTGTTGCCCGGG[C/G]GGCCGACCTCCGTGC | 389337 |
rs35477644 | in-del | -/C | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149612557 | GTCATAGTAATTCCC[-/C]AGTATTATGATATAT | 389337 |
rs35560041 | in-del | -/A | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149597111 | GTGGGATGGGGTGTA[-/A]GGGGGACCACTGGGA | 389337 |
rs35571373 | in-del | -/C | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149559499 | ATCTAACCAATCCTC[-/C]GTTGAGTATTCTGGT | 389337 |
rs35685128 | in-del | -/G | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149601997 | CTAACTGTGATGGGG[-/G]AGCCACTGGACAGTT | 389337 |
rs35751308 | in-del | -/C | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149568234 | GTTTCGCCATATTGC[-/C]TAGGTTGGTCTTGAA | 389337 |
rs35821132 | in-del | -/TA | 0.375 | 0.216506 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149577421 | TATTTACTTGACTCA[-/TA]GCATTGCGCGTATTG | 389337 |
rs35852760 | snp | C/T | 0.472429 | 0.114129 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149602987 | ACCCAGGCTGGAGTG[C/T]GATGGCATGATCTCG | 389337 |
rs35879891 | snp | A/T | 0.434253 | 0.168969 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149602798 | TGTCAGATTCACTAC[A/T]GTGGCAGAAAGGAGG | 389337 |
rs35884018 | snp | A/C | 0.473726 | 0.111565 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149562844 | ATGTCCTGTCCAGAG[A/C]TTTCTGCCTGTTCTA | 389337 |
rs35992063 | in-del | -/C | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149566821 | GTCATTCTACTCCCC[-/C]ACTTTCAATTTTATA | 389337 |
rs55634793 | snp | C/T | 0.0861826 | 0.188849 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149624419 | TTAAGTGAAATTAGA[C/T]GTAATGATGGGCAAC | 389337 |
rs55647643 | snp | C/T | 0.410737 | 0.191478 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149621540 | GCACTCTGTTAAGCT[C/T]ATTACATGCATCGTC | 389337 |
rs55658358 | snp | A/C | 0.0854556 | 0.188216 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149620014 | GGAGGCAGAGATTGC[A/C]ATGAGCCAAGATCAT | 389337 |
rs55696751 | in-del | -/A | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149589207 | CTTAAAAAAAAAAAA[-/A]GTTTTGAATATTGTT | 389337 |
rs55710354 | snp | C/T | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149598333 | TCTTCTTCTTTCTTC[C/T]TCTTCCTCTTCCTCT | 389337 |
rs55743857 | snp | A/G | 0.0861826 | 0.188849 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149585490 | AAGAAAGCCCCAGGC[A/G]AAAAACACTACATAG | 389337 |
rs55872372 | in-del | -/CC | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149598338 | TTCTTTCTTCCTCTT[-/CC]TCTTCCTCTTCTTCT | 389337 |
rs55915030 | snp | C/T | 0.165979 | 0.235458 | missense | ARHGEF37 | GRCh38.p7 | 5:149624064 | AGCTGGTGGAGGACG[C/T]ACTGGGCCGGACGAG | 389337 |
rs55996106 | snp | A/G | 0 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149558741 | TGTGTGTGTGTGTAT[A/G]TATATTTTTATATGT | 389337 |
rs56031520 | snp | C/T | 0.432504 | 0.170857 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149583425 | ACAGGCGTGAGCCAC[C/T]GTGCCTGGCCTATAG | 389337 |
rs56203037 | snp | A/G | 0.093417 | 0.194889 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149586649 | CAGGAGAAAGGTGGT[A/G]GAGGTTTAGACCCAG | 389337 |
rs56225846 | snp | C/T | 0.209997 | 0.246779 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149627663 | GGACCCTGGCTACAC[C/T]GCCAGAAGTCTGATG | 389337 |
rs56280149 | in-del | -/T | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149598328 | CTTCTTCTTCTTCTT[-/T]CTTCCTCTTCCTCTT | 389337 |
rs56331206 | in-del | -/CTC | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149598363 | TTCTTCTTCCTCTTC[-/CTC]TTCTTCCTCTTCCTC | 389337 |
rs56342926 | snp | C/T | 0.432504 | 0.170857 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149583610 | TAAACAGTGCCTTGG[C/T]TGATTCTGCCCTAGA | 389337 |
rs56396517 | in-del | -/CTGTCT | 0 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149576951 | ACAGAGTGAGAGACT[-/CTGTCT]GAAAAAAAAAATTGA | 389337 |
rs56822099 | snp | A/T | 0.453453 | 0.145282 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149592238 | TAAATTACAGAATAT[A/T]CTGTTGTAGACAATA | 389337 |
rs56862092 | in-del | -/TT | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149602073 | TCTTTTTTTTTTTTT[-/TT]GAGACGGAGTCTCAC | 389337 |
rs57077174 | snp | C/T | 0.254105 | 0.249966 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149607958 | TATTTTTAGTAGAGA[C/T]GGGATTTCATTGTGT | 389337 |
rs57165531 | snp | A/T | 0.396546 | 0.202545 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149555952 | AACATAGACCACATC[A/T]CTACAAAAATGTTTT | 389337 |
rs57292511 | snp | A/G | 0.0559525 | 0.157625 | synonymous-codon | ARHGEF37 | GRCh38.p7 | 5:149616765 | GATGCGCAAGGAAGT[A/G]GGTAAGGACTTGGGC | 389337 |
rs57382702 | snp | A/G | 0.0879971 | 0.190408 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149584918 | TGAGCCACCATGCCC[A/G]GCCTTCTTTATATGT | 389337 |
rs57459308 | snp | C/T | 0.0785177 | 0.181917 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149629947 | GTCAGATGCAAAAGG[C/T]CACATAGGATTCCAT | 389337 |
rs57536109 | snp | G/T | 0.108402 | 0.206034 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149616459 | GAGAGGGGGTGACTT[G/T]CCTGAGATCACACAG | 389337 |
rs57600055 | in-del | -/CTCT | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149604715 | TGAGACAGAATCTCT[-/CTCT]GTCGCCCAGGCTGGA | 389337 |
rs57656451 | in-del | -/AAAAAAAAAAA/AAAAAAAAAAAA | 0 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149620836 | TCCTTCTCAAAAAAA[-/AAAAAAAAAAA/AAAAAAAAAAAA]GAAGTCAGGCACTTT | 389337 |
rs57679147 | snp | C/T | 0.473818 | 0.111381 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149554075 | TGGGAGGCTGAGGCA[C/T]GAGAATCGCTTGAAC | 389337 |
rs57745588 | in-del | -/TTTATTTATTTA/TTTATTTATTTATTTATTTATTTATTTATTTA | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149599457 | TTATTTATTTATTTA[lengthTooLong]CAGGAGACAGGGTCT | 389337 |
rs57846231 | snp | C/G | 0.473726 | 0.111565 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149554404 | TTTTTTTTAGAACTT[C/G]TGTAAGCCCATTAAA | 389337 |
rs57933199 | in-del | -/GC | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149626288 | CACACACACACACAC[-/GC]CTCTCTCAAGACATA | 389337 |
rs58068266 | snp | G/T | 0.0221141 | 0.102801 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149594008 | CATGCTATTTTAAAT[G/T]GATATATAATAGTTG | 389337 |
rs58189209 | snp | C/T | 0.118933 | 0.212888 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149586900 | AGATACACTGGACTA[C/T]AGCATTCCTTTGATC | 389337 |
rs58190588 | in-del | -/A | | | upstream-variant-2KB, intron-variant | CSNK1A1, ARHGEF37 | GRCh38.p7 | 5:149553435 | CTTAAAAAAAAAAAA[-/A]GCCAAGTTTAAGCAT | 389337 |
rs58263212 | in-del | -/ACACAC | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149626282 | CACACACACACACAC[-/ACACAC]GCCTCTCTCAAGACA | 389337 |
rs58298279 | in-del | -/AA | | | upstream-variant-2KB, intron-variant | CSNK1A1, ARHGEF37 | GRCh38.p7 | 5:149552243 | AAAAAAAAAAAAAAA[-/AA]GAATCGTATGTTGGT | 389337 |
rs58319998 | snp | A/G | 0.18325 | 0.240924 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149600605 | CCCACTGAGTACTCC[A/G]TCTGTTCCTCTCTTC | 389337 |
rs58424921 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | CSNK1A1, ARHGEF37 | GRCh38.p7 | 5:149550494 | TAATTGGAACAAGAG[A/G]CCCAGTAGAATTAAG | 389337 |
rs58450062 | snp | C/T | 0.106633 | 0.204807 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149592739 | GGCTGTACCATTTTA[C/T]GTTTTCTTGTTTTTT | 389337 |
rs58720743 | in-del | -/T | | | intron-variant, upstream-variant-2KB | ARHGEF37 | GRCh38.p7 | 5:149595960 | TTTTTTTTTTTTTTT[-/T]CCTGATCCACCATTT | 389337 |
rs58921723 | snp | A/G | 0.0648419 | 0.167978 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149600350 | CTTTCCCACTTGAAT[A/G]TGTGTCCAGCACATC | 389337 |
rs58959997 | in-del | -/GTGTGTGTGTGTGT | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149558725 | TGTGTGTGTGTGTGT[-/GTGTGTGTGTGTGT]ATATATATTTTTATA | 389337 |
rs59260971 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149577521 | CAGCAAGTGATTCTA[A/G]TGATTAAAAAAAATG | 389337 |
rs59331907 | in-del | -/A | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149598798 | TAGATATAGATATAT[-/A]GATATATATATGTGT | 389337 |
rs59484704 | in-del | -/TTTA | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149585535 | TTATTTATTTATTTA[-/TTTA]GAGACGGATTCTTGC | 389337 |
rs59529358 | snp | A/G | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149558630 | TAAAGTGCTGGGATT[A/G]CAGGCGTGAGCCACT | 389337 |
rs59567777 | snp | A/G | 0 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149558739 | TGTGTGTGTGTGTGT[A/G]TATATATTTTTATAT | 389337 |
rs59844382 | snp | C/T | 0.473174 | 0.112665 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149554453 | CTTCTGGAAACCCTT[C/T]TAACCCTGAGATTCT | 389337 |
rs59883777 | snp | A/G | 0.339234 | 0.235883 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149585448 | TACATGCTTCCATAC[A/G]AATGGATCTCAAAAT | 389337 |
rs60009445 | in-del | -/TTCATTCA | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149629241 | TCATTCATTCATTCA[-/TTCATTCA]ATATTTGCCAGGCAC | 389337 |
rs60129185 | snp | C/G | 0.375 | 0.216506 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149558229 | AGACAGGGACTGACC[C/G]GGCACCATGGCTTAC | 389337 |
rs60692796 | snp | G/T | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149621282 | ACTGTGGGCAACATA[G/T]ACCCTGTCTCTACAA | 389337 |
rs60711347 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149599299 | TCATGGACACAGAGG[C/T]CTGCTCAGCCACAGG | 389337 |
rs60715194 | in-del | -/ATTT/ATTTATTT | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149556403 | TTTATTTATTTATTT[-/ATTT/ATTTATTT]TGAGATGGAGTCTCG | 389337 |
rs60829450 | snp | C/T | 0.208474 | 0.246527 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149585540 | TTATTTATTTAGAGA[C/T]GGATTCTTGCTCTGT | 389337 |
rs61191880 | snp | A/T | 0.0310518 | 0.120672 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149562462 | TTATTTATTTATTTA[A/T]TTTTGAGACGGAGTC | 389337 |
rs61396754 | in-del | -/GA | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149598791 | AGATATATAGATATA[-/GA]TATATAGATATATAT | 389337 |
rs61619155 | in-del | -/GTGTGTGTGTATAT | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149558729 | TGTGTGTGTGTGTGT[-/GTGTGTGTGTATAT]ATATTTTTATATGTA | 389337 |
rs62377976 | snp | G/T | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149575594 | TTGAAAAGACACAAA[G/T]TAGAGATGGCCCTTT | 389337 |
rs62377977 | snp | A/G | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149583618 | GCCTTGGCTGATTCT[A/G]CCCTAGATCAAATAA | 389337 |
rs62377978 | snp | G/T | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149587913 | TTTTTTTTTTTTTTT[G/T]GGAGACAAAGTCTCA | 389337 |
rs62377979 | snp | G/T | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149587915 | TTTTTTTTTTTTTTG[G/T]AGACAAAGTCTCACT | 389337 |
rs62378010 | snp | C/T | 0.371987 | 0.218218 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149620841 | TCTCAAAAAAAGAAG[C/T]CAGGCACTTTACACA | 389337 |
rs66748416 | snp | C/T | 0.421209 | 0.182174 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149611802 | TCAGTGCCATGCTCC[C/T]TTGTTATAACAAATA | 389337 |
rs66849337 | multinucleotide-polymorphism | CGG/TGA | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149598542 | CTGACAGTGACTTTG[CGG/TGA]TCGAATAAAGAGACC | 389337 |
rs66915990 | snp | A/G | 0.144969 | 0.226867 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149629796 | AGAAACAACCCACAG[A/G]CCCATCAATATGAAT | 389337 |
rs66982663 | in-del | -/TGGCAG | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149626959 | GGGTGGGCCCTTCAG[-/TGGCAG]AGTTAGGATCAGGCC | 389337 |
rs66996935 | in-del | -/AAAAAAAAAA/TAAAAAAAAAAA | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149620830 | GTGAGACTCCTTCTC[-/AAAAAAAAAA/TAAAAAAAAAAA]AAAAAAAGAAGTCAG | 389337 |
rs67057970 | snp | A/G | 0.147656 | 0.228091 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149618817 | CAGCTTTGGGGTTGC[A/G]AGAACCAGCTCTGGT | 389337 |
rs67079479 | in-del | -/AAAA | 0.375 | 0.216506 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149607777 | GCAAGACTCCATCTC[-/AAAA]AAAAAAAAAAAAAAA | 389337 |
rs67170555 | snp | C/G | 0.412416 | 0.190055 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149610183 | TTGGAGAAGCGGAAA[C/G]GTTTGGGAACAGTGC | 389337 |
rs67190306 | snp | A/G | 0.409382 | 0.192607 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149587339 | AACTTCATACATCTG[A/G]TCAATGGTAATGCTA | 389337 |
rs67630385 | in-del | -/CTCTGT | 0.409891 | 0.192184 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149576949 | CAACAGAGTGAGAGA[-/CTCTGT]CTGAAAAAAAAAATT | 389337 |
rs70973528 | in-del | -/AC | 0 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149558737 | TATAAAAATATATAT[-/AC]ACACACACACACACA | 389337 |
rs70973530 | in-del | -/AATT | 0 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149589342 | AGATCCTGTCTTATA[-/AATT]AATTAATTAATTAAT | 389337 |
rs70973531 | in-del | -/AAG | 0 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149598327 | AGAGGAAGAGGAAGA[-/AAG]AAGAAGAAGAAGAAG | 389337 |
rs70973532 | in-del | -/ATCTATATCTATAT | 0 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149598765 | TATCTATATCTATAT[-/ATCTATATCTATAT]CTATATCTATATATA | 389337 |
rs70973533 | in-del | -/AAA | 0 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149624916 | GTGAAACTCCATCTC[-/AAA]AAAAAAAAAAAAAAA | 389337 |
rs71274354 | in-del | ACTTC/GCTTCTTTTTTTTTTT | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149620837 | TGTGTAAAGTGCCTG[ACTTC/GCTTCTTTTTTTTTTT]TTTTTTTGAGAAGGA | 389337 |
rs71274355 | in-del | -/AC | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149598823 | TATACATATATATAT[-/AC]ACACACACACACACA | 389337 |
rs71584000 | multinucleotide-polymorphism | CA/TG | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149554075 | TGGGAGGCTGAGGCA[CA/TG]AGAATCGCTTGAACT | 389337 |
rs71584001 | in-del | -/A | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149561261 | CTGGGCAACAGAGCA[-/A]GACTCTGTCTCAAAA | 389337 |
rs71586128 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149594401 | GCAGATCACGGGGTG[C/T]GTTTGGGAGCCAGAA | 389337 |
rs71586129 | snp | A/G | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149608246 | GGATATGATGGCTTA[A/G]CTTGTGCTCAGAGGC | 389337 |
rs71586130 | snp | A/C/G | 0.000248396 | 0.0111416 | missense, utr-variant-5-prime | ARHGEF37 | GRCh38.p7 | 5:149609644 | TGGTGGACACGTACC[A/C/G]GAAGGAGCCGGAGCT | 389337 |
rs71586131 | snp | A/G | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149609990 | GCAGCCACTGTCTGG[A/G]ATATTGCCAGTAACT | 389337 |
rs71586412 | multinucleotide-polymorphism | CTC/TTT | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149618685 | CAAGGGTTTTACCCT[CTC/TTT]GGAGTTTCTGTTTTC | 389337 |
rs71586413 | in-del | CATATA/TATATATATCTATATATC | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149598791 | ACACACACACACACA[CATATA/TATATATATCTATATATC]TATATCTATATATCT | 389337 |
rs71587780 | in-del | -/T | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149589338 | AATTAATTAATTAAT[-/T]AATTTATAAGACAGG | 389337 |
rs71587781 | multinucleotide-polymorphism | AAA/TTT | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149597269 | TTATCTATTAAAAAA[AAA/TTT]TTTTTTTTGTAAGAA | 389337 |
rs71587782 | in-del | -/CTC | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149598263 | TGCTTAAACTGACTC[-/CTC]TTCTTCTTCTTCTTC | 389337 |
rs71587783 | in-del | -/T | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149602493 | TCTCCTTTGGTTTAA[-/T]TTTTTTTTTTTTGAG | 389337 |
rs71587785 | in-del | -/T | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149615320 | TTTTTTTTTTTTTTT[-/T]GAAGCAGAGGTCATG | 389337 |
rs71905423 | in-del | -/ATTCATTC | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149629216 | AGCAGGGCAAGTGAG[-/ATTCATTC]ATTCATTCATTCATT | 389337 |
rs71932310 | in-del | -/C/TCT | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149598264 | CTTCTTCTTCTTCTT[-/C/TCT]CTTCTTCTTCTTCTT | 389337 |
rs72101227 | in-del | -/ATTC | 0.491346 | 0.0652092 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149629216 | AGCAGGGCAAGTGAG[-/ATTC]ATTCATTCATTCATT | 389337 |
rs72166213 | in-del | -/CTTT | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149631172 | TTCCTTCCTTCCTTT[-/CTTT]TTTTCTTTTTTTTTT | 389337 |
rs72241642 | in-del | -/TCTC | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149604710 | TTTTTTGAGACAGAA[-/TCTC]TCTCTGTCGCCCAGG | 389337 |
rs72285782 | in-del | -/AT | 0.428937 | 0.17459 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149577420 | GTATTTACTTGACTC[-/AT]AGCATTGCGCGTATT | 389337 |
rs72335484 | in-del | -/AGAG | 0.449853 | 0.150196 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149584365 | TTTTTCCTCCAGGAA[-/AGAG]AGAGAGAATGTGTAT | 389337 |
rs72823574 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149563073 | TCATCGTGTCTGAAT[C/T]TCAAACCCAGCAGTT | 389337 |
rs72823588 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149601991 | GTTTATTCTAACTGT[C/G]ATGGGGAGCCACTGG | 389337 |
rs72828312 | snp | C/T | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149627443 | AGTTTAGAGTGACTC[C/T]GTGGGACATGAAAAG | 389337 |
rs72828313 | snp | G/T | 0.0614824 | 0.164198 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149627499 | TTGCAGGGTCTACCA[G/T]GAAGCACCTATGGTG | 389337 |
rs73267830 | snp | C/T | 0.17461 | 0.238362 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149568179 | GTGTGCACCACCACG[C/T]CTGGCTAATTTTTTT | 389337 |
rs73267837 | snp | G/T | 0.0861826 | 0.188849 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149582346 | TGCTACTCAGGCAGG[G/T]TGGTTTCAGAGCACT | 389337 |
rs73267839 | snp | A/C | 0.104149 | 0.203046 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149583320 | TTTTTGTATTTTAGT[A/C]GAGATGGGGTTTCAC | 389337 |
rs73267876 | snp | A/G | 0.421368 | 0.182025 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149603142 | TTCACCATGTTGGCC[A/G]GGCTGGTCTCGAGCT | 389337 |
rs73267879 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149605885 | CTTGACCATGCTGCC[C/T]CCCTTTCTCTCCTTT | 389337 |
rs73267892 | snp | C/T | 0.156319 | 0.231784 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149613663 | AGAATTTTTATGAGG[C/T]TGCTTCTATACATGC | 389337 |
rs73267895 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149614866 | AGAGGCACGAGTATC[A/G]TCAGGGAGGGCCCAG | 389337 |
rs73269946 | snp | A/T | 0.0452528 | 0.143452 | downstream-variant-500B | ARHGEF37 | GRCh38.p7 | 5:149635327 | CCTGGAAGAGGTGAT[A/T]TCCAAGCTGAGGCCC | 389337 |
rs73796203 | snp | A/G | 0.209997 | 0.246779 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149628179 | CAGCTCCACCACTTT[A/G]CTGACTGTGTGATCT | 389337 |
rs73798249 | snp | A/C | 0.0551013 | 0.156571 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149607455 | CCAAGTACATCCCCC[A/C]CCATTTTCTAACTCT | 389337 |
rs73798250 | snp | C/T | 0.0170013 | 0.090618 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149609740 | CCTACCCCACTGACC[C/T]GGTTCAGGAGCAGCT | 389337 |
rs74294135 | snp | A/C | 0.122064 | 0.214785 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149576264 | GCAAACAAATAAACA[A/C]AGAAATTGTAAAATA | 389337 |
rs74327623 | snp | G/T | 0 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149631198 | TTTTTTTTTTTCGGG[G/T]TCTGGCTCTGTGGCC | 389337 |
rs74353647 | snp | A/G | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149601790 | GAGAATATCTGAAGG[A/G]AGAGTAGAGAGCATA | 389337 |
rs74354702 | snp | A/T | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149628799 | TGCTAACCTTCTGCA[A/T]GCTCCCTAGGACATC | 389337 |
rs74434699 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149614395 | CAGCTCTGTGTATCA[C/T]CTTTCAATTTCTGTT | 389337 |
rs74480837 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149609806 | TTCACGAGTGTTGCT[C/T]TGTCAGAGCCTGTGT | 389337 |
rs74558018 | snp | G/T | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149613780 | TTTTTTTTTTTTTTT[G/T]TGAGACAAGGTCTCA | 389337 |
rs74564350 | snp | A/G | 0.12932 | 0.218944 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149570604 | AAAGTTTGGCCAGGC[A/G]CGGTGGCTCACACCT | 389337 |
rs74677915 | snp | A/T | 0.148996 | 0.228688 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149602800 | TCAGATTCACTACAG[A/T]GGCAGAAAGGAGGAG | 389337 |
rs74770708 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ARHGEF37 | GRCh38.p7 | 5:149596145 | TCAGCTGCTCCCCAC[C/T]GTAGTTTTCAATTCC | 389337 |
rs74776845 | snp | A/T | 0.175897 | 0.238765 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149572927 | CTAGGTAATTTATTT[A/T]AAAAAAAAATTTATT | 389337 |
rs74821431 | snp | C/T | 0.0700422 | 0.173537 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149561673 | TTTCGCCTGTGTTTC[C/T]TATCCCACTCCCATT | 389337 |
rs74824261 | snp | A/G | 0.419776 | 0.18351 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149554076 | GGGAGGCTGAGGCAT[A/G]AGAATCGCTTGAACT | 389337 |
rs74850289 | snp | A/T | 0.172028 | 0.23753 | upstream-variant-2KB, intron-variant | CSNK1A1, ARHGEF37 | GRCh38.p7 | 5:149552894 | TTAACTGCAACTTTG[A/T]AAGGTGGTCAAGTAA | 389337 |
rs74883481 | snp | A/G | 0.081446 | 0.184634 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149564159 | ACAGGGTTTCGCTGT[A/G]TTGACCAGGCTGGTC | 389337 |
rs74951154 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149565522 | AATGGGCAAAAGCAT[A/T]CTGGCTACCAAGAGA | 389337 |
rs75027223 | snp | G/T | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149609984 | CTCACAGCAGCCACT[G/T]TCTGGAATATTGCCA | 389337 |
rs75113392 | snp | C/T | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149631148 | TTTCTTCCTTCCTTC[C/T]TTCCTTCCTTCCTTC | 389337 |
rs75140667 | snp | C/T | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149588227 | TTGTTTGTTTGTTTG[C/T]TTGCTTTGAGACAGA | 389337 |
rs75185680 | snp | A/G | 0.103082 | 0.202275 | upstream-variant-2KB, intron-variant | ARHGEF37 | GRCh38.p7 | 5:149580218 | GGTGTGCACCACCAC[A/G]CCCAGCTAATTTTTC | 389337 |
rs75265029 | snp | G/T | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149600657 | TAATTTTTTTTTTTT[G/T]TGAGATGGAGTCTCG | 389337 |
rs75279585 | snp | A/G | 0.00752376 | 0.060871 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149629004 | GGCTTGCCTCCCATC[A/G]GCCATCCGGACTGTG | 389337 |
rs75346863 | snp | A/T | 0.106987 | 0.205054 | downstream-variant-500B | ARHGEF37 | GRCh38.p7 | 5:149635235 | CGTGTAAGTGTCAGG[A/T]TGAAGTAATGGCAGG | 389337 |
rs75375636 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | CSNK1A1, ARHGEF37 | GRCh38.p7 | 5:149552183 | AAAATTAATTTAACA[A/G]GAGTGAAAAAACTGT | 389337 |
rs75398219 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149616388 | GGCCCAGAACCGTCA[C/T]TGCCTGCCTAACATC | 389337 |
rs75449679 | snp | A/T | 0.000399281 | 0.0141238 | missense, intron-variant | ARHGEF37 | GRCh38.p7 | 5:149620426 | GTGCAGTATTGCAAT[A/T]TGGCAAGAGACCTTC | 389337 |
rs75464155 | snp | A/T | 0.254385 | 0.249962 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149606462 | CCAACACAGACCTTG[A/T]CTGGGTCACAGGTCT | 389337 |
rs75468400 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149554536 | CACCATTCCAACACT[A/G]ACAGTGCCCAGCAAA | 389337 |
rs75468957 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149628751 | CATGGATTTTCTCCC[A/T]CATTAAAAGGGACGG | 389337 |
rs75478176 | snp | A/G | 0.00196693 | 0.0312985 | intron-variant, upstream-variant-2KB | CSNK1A1, ARHGEF37 | GRCh38.p7 | 5:149550797 | GGTGGTGGGGGGAAT[A/G]AGTAAAAGCGCAGCG | 389337 |
rs75624879 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149591681 | GATGGTGCAAAAATG[A/G]TACACATTCAGTAGA | 389337 |
rs75630458 | in-del | -/AAGTA | 0.406641 | 0.194842 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149586235 | GGGTTTCAAGCAGAG[-/AAGTA]AAGTGACAAATTTTA | 389337 |
rs75631873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149564252 | CAGTGCTTTATACAA[C/T]ATTAGTCTTACGTAT | 389337 |
rs75678335 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149625530 | CTGGCCCAAGTGCCG[C/T]GAACATGGGAGACCT | 389337 |
rs75684240 | snp | C/T | 0.00231657 | 0.0339546 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149601253 | AAAAAACCTAAGGAG[C/T]TGTCAGCCTTAGATT | 389337 |
rs75689644 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149593711 | TAGAGAAAAGAAAAC[A/G]TTATTTAAAAAATCA | 389337 |
rs75740782 | snp | C/G | 0.0295035 | 0.117819 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149622937 | TGTGTGTCACAGTCT[C/G]CAGCTCAGCTTTTCC | 389337 |
rs75799689 | snp | A/G | 0.0154464 | 0.0865136 | synonymous-codon, utr-variant-5-prime | ARHGEF37 | GRCh38.p7 | 5:149609654 | GTACCGGAAGGAGCC[A/G]GAGCTGCAGCGGCAC | 389337 |
rs75835733 | snp | A/G | 0.110167 | 0.207236 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149601704 | TCATGGTAACTTCTG[A/G]GTGTGAGGGAAGGCC | 389337 |
rs75849771 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149617052 | TGCACACCACACTTA[C/T]CCGGGTAAGGCAGGG | 389337 |
rs75871958 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149618097 | GGGCCCAAGCAGGTG[C/T]CCAGCCGGGCATGTC | 389337 |
rs75881609 | snp | C/T | 0.0678174 | 0.1712 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149618584 | AGCCCTAAATAGCTA[C/T]TTCTAGCAGCACAGG | 389337 |
rs75885888 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149574931 | CTTCCTAAATGATTT[A/C]TCACCTCAGCCTTAT | 389337 |
rs75959466 | snp | C/T | 0.146985 | 0.227789 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149629877 | GAGACGAATGAAACA[C/T]CGGTACATGCTGCAG | 389337 |
rs76021776 | in-del | -/T | 0.34303 | 0.232046 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149568922 | TAACAACTGTTCTGA[-/T]TTTTTTTTATCATAG | 389337 |
rs76089877 | snp | C/T | | | missense, utr-variant-5-prime, upstream-variant-2KB | CSNK1A1, ARHGEF37 | GRCh38.p7 | 5:149550169 | TCTGAGATTCTAGCT[C/T]CACTGCCACTTCCTG | 389337 |
rs76100063 | snp | C/T | 0.42 | 0.183303 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149555776 | AAATTAGGACAATCA[C/T]GTCCCAGGGATTACT | 389337 |
rs76177022 | snp | A/C | 0.122064 | 0.214785 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149588416 | ATTTTTGTGTCTCAG[A/C]CACCCAAGTAGCTGA | 389337 |
rs76200750 | snp | A/G | 0.122064 | 0.214785 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149584462 | ATTTATCAACACAGA[A/G]AAGTCCTTTTCTGTA | 389337 |
rs76206409 | snp | A/G | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149586239 | TTCAAGCAGAGAAGT[A/G]AAGTGACAAATTTTA | 389337 |
rs76318372 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149610251 | ACCCATGTGTTCCCA[A/T]AGTGATAAGAAGCAG | 389337 |
rs76511535 | snp | A/C | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149628798 | CTGCTAACCTTCTGC[A/C]TGCTCCCTAGGACAT | 389337 |
rs76554597 | snp | A/G | 0.0681886 | 0.171594 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149610630 | GCTCCCAAAAAAACT[A/G]TATTCATTTTCCCTT | 389337 |
rs76576966 | snp | A/G | 0.0528381 | 0.153711 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149610034 | AAAGAGCTCTGGAGA[A/G]TCTAATGCTGGCAAT | 389337 |
rs76589288 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149575447 | TGGCTCTATGCTCAG[A/G]GGACTGACCCAGTGA | 389337 |
rs76624497 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149620180 | TGACTCAGTCTAAGG[C/T]GGAACTTTCTAATCA | 389337 |
rs76641595 | snp | A/C | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149584205 | CTGCTTTAAAAAAAA[A/C]CTGTGTTGTCTCCTT | 389337 |
rs76797980 | snp | A/C | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149591228 | TTGTGTTCCATCTCA[A/C]AAAAAAAAAAAAAGT | 389337 |
rs76829940 | in-del | -/CCTGACATATATAATAAATATATTACATATGTAATA | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149608261 | GCTTGTGCTCAGAGG[lengthTooLong]TGACATATATAATAA | 389337 |
rs76855023 | snp | A/C | 0.172351 | 0.237636 | upstream-variant-2KB, intron-variant | CSNK1A1, ARHGEF37 | GRCh38.p7 | 5:149552895 | TAACTGCAACTTTGA[A/C]AGGTGGTCAAGTAAT | 389337 |
rs76859006 | snp | A/G | 0.0146672 | 0.084371 | utr-variant-3-prime | ARHGEF37 | GRCh38.p7 | 5:149632654 | ACATGGTATCAGGAG[A/G]CATCATAACCAATGA | 389337 |
rs76878779 | snp | A/T | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149560082 | ACAGTGAGCCAAGTA[A/T]GAGAAAAAGTAATCT | 389337 |
rs76892686 | snp | A/C | 0.0123036 | 0.0774623 | utr-variant-3-prime | ARHGEF37 | GRCh38.p7 | 5:149634865 | TGAGGACAAGATTAC[A/C]ATATCAAAAGAAAGA | 389337 |
rs76903554 | in-del | -/C | 0.128976 | 0.218754 | upstream-variant-2KB, intron-variant | CSNK1A1, ARHGEF37 | GRCh38.p7 | 5:149552391 | AGAATCAAATTTTGA[-/C]CACGTTTTGTTTTAC | 389337 |
rs76975328 | snp | C/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | ARHGEF37 | GRCh38.p7 | 5:149579614 | TGGGACAGAGTCTCA[C/G]TCTGTCGCCCAGGCT | 389337 |
rs77063086 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149562008 | TGAGACTAAATTTGG[A/G]AGATGCTTGAGTTGC | 389337 |
rs77130603 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149562299 | TTTATATGGCACTGT[A/G]TAGTTCATAGAGTAT | 389337 |
rs77154863 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149630010 | AGATAGAAGGTGGAT[A/G]AATGGCAGGGGCTGG | 389337 |
rs77311285 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149607365 | AATACTTGGTGCTGC[C/T]CTTCCCTTGCTTGTT | 389337 |
rs77391819 | snp | C/T | 0.0103381 | 0.0711491 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149623966 | AGCCAGGGATCTCAT[C/T]GTCCCCTCTTGCCCA | 389337 |
rs77394904 | snp | C/T | 0.12932 | 0.218944 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149565113 | AGGAGATTGAGCAAA[C/T]CTGTGGTGCTTTCAG | 389337 |
rs77453953 | snp | A/G | 0.247337 | 0.249986 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149572568 | GGACTTGTGAGGGTT[A/G]ACGTATCAACTTGGC | 389337 |
rs77454787 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149584427 | CTGTTGCTGTCTTTC[C/T]GCCTCACTTCCAATC | 389337 |
rs77489920 | snp | A/G | 0.0718919 | 0.175435 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149622334 | GAAGAAGCTTTGCTC[A/G]TACAATGGCAGATCT | 389337 |
rs77584784 | snp | A/G | 0.108402 | 0.206034 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149621455 | AAAAAAAAACAAAAA[A/G]CTTTTTCAAGGTCTT | 389337 |
rs77616515 | snp | A/G | 0.0577344 | 0.159793 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149561582 | AAATTCAAGTCATCA[A/G]TGTTCCATCTACTCA | 389337 |
rs77742583 | snp | C/G | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149628800 | GCTAACCTTCTGCAT[C/G]CTCCCTAGGACATCG | 389337 |
rs77764032 | snp | A/T | 0.107341 | 0.205301 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149629352 | GAGTAGGGAAAACAG[A/T]GATTAAGAAAATAAT | 389337 |
rs77796084 | snp | A/G | 0.123452 | 0.215605 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149579060 | GGGATCCTATAATAC[A/G]GCAGCTGCCCCGGGG | 389337 |
rs77818054 | snp | C/T | 0.0528381 | 0.153711 | upstream-variant-2KB, intron-variant | CSNK1A1, ARHGEF37 | GRCh38.p7 | 5:149553482 | GTTTTCCAGAGATCA[C/T]TCCTTTTCTGCTAAT | 389337 |
rs77823588 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149585965 | TCATTGACAATTTGA[C/T]ATTTATTCTGCCAGT | 389337 |
rs77848381 | snp | C/G | 0.107341 | 0.205301 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149628297 | TGAAGACTATGTAAT[C/G]AAATGCTTGCTCTGT | 389337 |
rs77870785 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149557779 | CATTTATTTCAATTA[A/C]TGTTATTTTTTGAAT | 389337 |
rs77960326 | snp | C/T | 0 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149558303 | TTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 389337 |
rs77983671 | snp | C/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | CSNK1A1, ARHGEF37 | GRCh38.p7 | 5:149552558 | AAATAGAAATGGGGG[C/G]CGGGCGCAGTGGCTC | 389337 |
rs78009044 | snp | A/G | 0.122064 | 0.214785 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149583591 | GATCAGCAGATTACT[A/G]TGGTAAACAGTGCCT | 389337 |
rs78031003 | snp | A/G | 0.0752113 | 0.178743 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149593741 | ATGGAGAAGAGAAAA[A/G]ATGTTTACTATTCGC | 389337 |
rs78140978 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149582459 | ATAGTTTAACCTTTT[C/T]AAGGCCTAGTTTTAT | 389337 |
rs78211769 | snp | A/T | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149609205 | AAACAAAAAAACAAA[A/T]AAACAAGCTAATGGT | 389337 |
rs78295033 | snp | C/T | 0.0528381 | 0.153711 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149563474 | TTCAAGTTCTGTCAT[C/T]CTTCTTAGCCTGTAT | 389337 |
rs78367835 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149553725 | TGAGGATGTGAGAAA[A/T]GTAAGCAATACATCT | 389337 |
rs78380792 | snp | G/T | 0 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149590608 | CTTTTTTTTTTTTTT[G/T]AGGCAGAATTTCACT | 389337 |
rs78412086 | snp | G/T | 0.108402 | 0.206034 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149619161 | AAACCAACCAGATGA[G/T]GTCATCCTGTCTCAT | 389337 |
rs78479898 | snp | A/G | 0.392881 | 0.205147 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149592577 | TTCCAGTTTTTGAAT[A/G]TTACAAATAAAGCTT | 389337 |
rs78611877 | snp | A/T | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149629367 | TGATTAAGAAAATAA[A/T]TTCATGACTAACTGA | 389337 |
rs78618835 | snp | A/G | 0.0125231 | 0.0781326 | missense | ARHGEF37 | GRCh38.p7 | 5:149619019 | CTGAAGAACAACGTG[A/G]CTGCTTACCTGGACA | 389337 |
rs78619339 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149615280 | CTGCCTTAGCCTCCT[G/T]AGTAGCCACCACCAT | 389337 |
rs78637208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149602031 | AGTGGGGAAGTGACA[C/T]GGTTTGATTTATGTT | 389337 |
rs78682810 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149617744 | CTGCTTCTCCATCCT[A/G]CGACAGATCAGTAGG | 389337 |
rs78711777 | snp | C/G | 0.121369 | 0.214369 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149575886 | CCCTGCCGTCCCCCC[C/G]CTCAAAAAATACAAA | 389337 |
rs78792555 | snp | A/T | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149584207 | GCTTTAAAAAAAAAC[A/T]GTGTTGTCTCCTTCC | 389337 |
rs78818953 | snp | A/T | 0.375996 | 0.215928 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149591387 | CGTGCTCGGCCAGCC[A/T]TTGTCTTTTTTTAAG | 389337 |
rs78819112 | snp | G/T | 0.00446286 | 0.0470267 | missense | ARHGEF37 | GRCh38.p7 | 5:149627164 | TGACAAGCAACATCA[G/T]TGGGACTGGGACTCT | 389337 |
rs78820823 | snp | C/T | 0.284665 | 0.2476 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149621720 | CGACTCCCACGCTCA[C/T]GTCTCCCCACAGAAG | 389337 |
rs78826121 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | ARHGEF37 | GRCh38.p7 | 5:149596399 | AACCTCCACCTCCTG[A/G]GTTCAAGTGATTCTC | 389337 |
rs78862797 | snp | C/G | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149589865 | AGAGATGGGGTCTCA[C/G]TGTGTTTCCCAGGCT | 389337 |
rs78919004 | snp | C/G | 0.336702 | 0.234484 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149574496 | TTTCTTTGCCTGCCC[C/G]TTGGTTGTGTTCACC | 389337 |
rs78919139 | snp | A/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | ARHGEF37 | GRCh38.p7 | 5:149595945 | TGTGTGGATAGCTGC[A/T]TTTTTTTTTTTTTTT | 389337 |
rs79065170 | snp | G/T | 0.0498117 | 0.149749 | upstream-variant-2KB, intron-variant | ARHGEF37 | GRCh38.p7 | 5:149580476 | TTCTGAGTGTAGAGT[G/T]GTGGTTAAGCAGCCT | 389337 |
rs79209160 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149612834 | TTCTCAGTCTGCTAT[C/G]ATAGATGGCACCAGG | 389337 |
rs79210122 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149587540 | TGCAGAATCAGCATT[C/T]GAAATGACATTTTTC | 389337 |
rs79232537 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149577563 | AAGTATTAGTGCTAT[A/G]AAGAAGTTCTCTGAT | 389337 |
rs79315610 | snp | C/T | 0.030278 | 0.119257 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149605511 | AGTGCCCAATAGCCA[C/T]GTGTGGCTGGTGACT | 389337 |
rs79320119 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149593050 | GCTGAGATTACAGGT[A/G]TAAGCCGCTGTACCC | 389337 |
rs79344454 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149619716 | TTTTAATGCATTGAT[A/G]TAAATAGGAAAAGTT | 389337 |
rs79352477 | snp | C/T | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149613766 | TCTACAGTGTTTTCT[C/T]TTTTTTTTTTTTTTT | 389337 |
rs79389450 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149582180 | TTACAGTGGGGAAGC[A/G]GACAGCCTGCCCAGG | 389337 |
rs79393945 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149625675 | TGTGCCGTGGGCCCC[A/G]AGACTCGGGGAGAGA | 389337 |
rs79552048 | snp | A/G | 0.0193772 | 0.0965046 | utr-variant-3-prime | ARHGEF37 | GRCh38.p7 | 5:149634277 | CTGGTGCCAGAGATG[A/G]CCATGAGCTGTAAGC | 389337 |
rs79558684 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149583376 | TCCTGAGCTCAGGCA[A/G]TTGCCTACCTCGGCC | 389337 |
rs79642983 | snp | G/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | ARHGEF37 | GRCh38.p7 | 5:149580630 | GATACCTATCTCTTA[G/T]AGAAATTGTGAATGA | 389337 |
rs79642987 | snp | A/G | 0.0833327 | 0.186341 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149601265 | GAGTTGTCAGCCTTA[A/G]ATTCTCATGGAACTG | 389337 |
rs79689246 | snp | A/G | 0.0528381 | 0.153711 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149629755 | ATGCGTGTTCATGGC[A/G]GCATTATTCATTGCA | 389337 |
rs79720240 | in-del | -/CTCA/TTCA | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149629248 | TCATTCATTCATTCA[-/CTCA/TTCA]ATATTTGCCAGGCAC | 389337 |
rs79751727 | snp | C/T | 0.0770498 | 0.180522 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149606518 | GGTCAGCTGGGCTTC[C/T]TGTGGTCCCTGGTTC | 389337 |
rs79804289 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149597652 | TGACTCTGTTTGCAG[C/T]TTAAGATGTTTTTAG | 389337 |
rs79842757 | snp | A/G | 0.107341 | 0.205301 | downstream-variant-500B | ARHGEF37 | GRCh38.p7 | 5:149635343 | TCCAAGCTGAGGCCC[A/G]GTGGGTGGTTAGGTG | 389337 |
rs79862650 | snp | A/G | 0.122411 | 0.214991 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149589040 | TTAGAGACCAGCCTC[A/G]GAAACAAGTGAGACC | 389337 |
rs79863700 | snp | A/T | 0.0356815 | 0.128715 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149629933 | GCTAAGTGAACAAAG[A/T]CAGATGCAAAAGGCC | 389337 |
rs79888176 | snp | C/T | 0.122758 | 0.215196 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149583226 | ACTGCAACCTCCGCC[C/T]CCCGGGTTCAAGCAA | 389337 |
rs79899373 | snp | C/G | 0.030278 | 0.119257 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149581997 | ACAAACAATGGTAAA[C/G]AATCCTTGCCAAGCA | 389337 |
rs79916383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARHGEF37 | GRCh38.p7 | 5:149594789 | GCACAAAACAACAAA[C/T]ACCCACGTACTTACC | 389337 |
rs79935494 | snp | G/T | 0.0236746 | 0.106192 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149563190 | AGACAATGCTGCTTA[G/T]TCCTGCTTCATCAGT | 389337 |
rs79937398 | snp | G/T | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149571930 | AAAAAAAAAAAAGAA[G/T]TTGACAAGCTGATTT | 389337 |
rs79956793 | snp | C/G | 0.0119091 | 0.0762411 | utr-variant-3-prime | ARHGEF37 | GRCh38.p7 | 5:149633498 | TCAAAAACAGTTCCT[C/G]TTCAAGGAGGACTGA | 389337 |
rs79958564 | snp | A/G | 0.0640965 | 0.167152 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149554155 | CCTGGGCAAGAGAGT[A/G]AGACTTTGTCTCAAA | 389337 |
rs80040768 | snp | A/G | 0.158302 | 0.232576 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149630188 | AGTATTATAGAATGT[A/G]AATTATATCTGAAAA | 389337 |
rs80098749 | snp | C/T | 0.119281 | 0.213102 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149576329 | CAGGCTTTGAAGTCA[C/T]ACTTCTGAGGTTTCA | 389337 |
rs80188608 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149610000 | TCTGGAATATTGCCA[A/G]TAACTGTGGCTTAAG | 389337 |
rs80219591 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149600799 | CACCCACCACCATGC[C/T]GAGCTAATTTTTGTA | 389337 |
rs80269407 | snp | A/C | 0.5 | 0 | upstream-variant-2KB, intron-variant | CSNK1A1, ARHGEF37 | GRCh38.p7 | 5:149552210 | CTGTTATGTCCCCTC[A/C]ACCCCACCAAAAAAA | 389337 |
rs80269834 | snp | G/T | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149613782 | TTTTTTTTTTTTTTT[G/T]AGACAAGGTCTCACT | 389337 |
rs80273051 | snp | A/G | 0.0352966 | 0.128072 | upstream-variant-2KB, intron-variant | CSNK1A1, ARHGEF37 | GRCh38.p7 | 5:149553388 | CTGGAGACAGAGCGA[A/G]ACTCCACTCCATCTA | 389337 |
rs80324589 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149578259 | TGGACTCTGGCTAGT[A/G]ACTAGTCTTTAGGTA | 389337 |
rs111306933 | snp | A/G | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149571927 | AAAAAAAAAAAAAAA[A/G]AAGTTGACAAGCTGA | 389337 |
rs111408071 | snp | G/T | 0.444444 | 0.157135 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149575777 | ACCTCTGCCTCCCGG[G/T]TTCAAGCAGTTCTCC | 389337 |
rs111486859 | snp | A/C | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149582674 | GTTCTAGCATAAAGA[A/C]AAATATTTAAAGTGA | 389337 |
rs111493169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149609803 | TGCTTCACGAGTGTT[A/G]CTCTGTCAGAGCCTG | 389337 |
rs111494355 | snp | C/G | 0.0422008 | 0.138995 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149619229 | AGGCCATTATACTGG[C/G]GGCAGCTCCGAGCCC | 389337 |
rs111536823 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149613141 | GATAACCTTCTTTGT[A/T]TTCCTTTATCAGCTA | 389337 |
rs111605134 | snp | C/T | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149605300 | ATTTTCAAGTAGCTA[C/T]ATTAAGAAAATTAAA | 389337 |
rs111648294 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149557522 | TCTCCTTCTGTTGCC[C/T]ATGCTGGAGTGCAGT | 389337 |
rs111671134 | in-del | -/T/TT | 0.337158 | 0.234315 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149554647 | AGAATGGCAAAATTG[-/T/TT]TTTTTTTTTTTTTTT | 389337 |
rs111672590 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149559703 | TGTGGTGATTAAACC[C/T]GTATTCATGGACTAT | 389337 |
rs111675901 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CSNK1A1 | GRCh38.p7 | 5:149549921 | AATTTACTCAGTAAT[C/T]GAGATGACTGACTTA | 389337 |
rs111750588 | snp | A/G | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149569009 | TAGTATGTGCTCTTT[A/G]TGTCCAGCTTCTTTT | 389337 |
rs111777652 | snp | A/G | 0.438386 | 0.164349 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149558737 | TGTGTGTGTGTGTGT[A/G]TATATATATTTTTAT | 389337 |
rs111790943 | snp | C/G | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149614215 | TGTACCTTTATCTTT[C/G]CTCACTTGGGTTTGG | 389337 |
rs111857021 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149593481 | TTTAAGATTCATTCA[A/T]GTTGTAGAACATATG | 389337 |
rs111893805 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149612848 | TGATAGATGGCACCA[A/G]GTTATTAGATTCCTT | 389337 |
rs111948844 | in-del | -/A | 0 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149620687 | TACAGAAAATTAGCC[-/A]GGGCATGGCAGTGTG | 389337 |
rs111955282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149612523 | TAACACCGTTGAAAT[C/T]GGGATTTATAAAAGA | 389337 |
rs111974132 | snp | C/T | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149592797 | TTGTTTGAGATGGAG[C/T]CTCGCTCTGTCATCC | 389337 |
rs112027992 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149575315 | TCTTTGGCTCCCTAA[G/T]TTCCCTATAGAATTG | 389337 |
rs112057100 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149626782 | ACTTACCCTGACGGT[A/G]TGGGCAGAATTTAGG | 389337 |
rs112089644 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149606480 | GGGTCACAGGTCTAG[C/T]CCATGGCTTTGGCAG | 389337 |
rs112280784 | snp | C/T | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149619569 | TGCTGGGTGAGAATA[C/T]GGGCCCAGTTCTTCT | 389337 |
rs112301925 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149574003 | ATAAACATCCTTATG[C/T]GAATATCTTTATATA | 389337 |
rs112314949 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149558102 | GTCTCAAACTCCTGA[C/T]CTCAGGTGATCCACC | 389337 |
rs112357085 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149603090 | GGCGCCCGCCACCAC[A/C]CCCGGTTAATTTTTG | 389337 |
rs112463471 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | CSNK1A1, ARHGEF37 | GRCh38.p7 | 5:149550258 | AGGAGGGAGACATTA[C/G]CAAAACTCCAAGTCG | 389337 |
rs112469197 | snp | A/G | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149623056 | CAGCTGCTGGATGTG[A/G]CCACTCTGCACAGAC | 389337 |
rs112566239 | in-del | -/TT | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149598266 | TGCTTAAACTGACTC[-/TT]CTTCTTCTTCTTCTT | 389337 |
rs112618028 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ARHGEF37 | GRCh38.p7 | 5:149596373 | GCAGTGGCACAATCT[C/T]GGCTCACTGCAACCT | 389337 |
rs112623210 | snp | C/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | ARHGEF37 | GRCh38.p7 | 5:149580310 | GTGATCTGCCCCCCC[C/G]TCAGCTTCCCAAAGT | 389337 |
rs112629591 | snp | C/T | 0.335559 | 0.234904 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149575742 | GCTGGAGTGCAGTGA[C/T]GCAATCTCAGCTCAC | 389337 |
rs112650223 | snp | G/T | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149565861 | TTTTTTTTTTTTTTT[G/T]TTTGTGAGACAGAGT | 389337 |
rs112721268 | snp | A/G | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149618686 | AAAACAGAAACTCCG[A/G]GAGGGTAAAACCCTT | 389337 |
rs112743118 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149590328 | ACTCTGTTGCCCAGG[C/T]TGGAGTGCAGTGGCA | 389337 |
rs112748528 | snp | C/G/T | 0.00636936 | 0.0560724 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149602975 | TCTCGCTCTGTCACC[C/G/T]AGGCTGGAGTGCGAT | 389337 |
rs112755666 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | ARHGEF37 | GRCh38.p7 | 5:149595562 | TGTTTCTGTTTTGGC[C/G]TGTATCTGACTGGTT | 389337 |
rs112818050 | snp | A/G | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149616119 | ATAGGACCAAATGAG[A/G]TCACTAAGAGAAAGT | 389337 |
rs112833884 | in-del | -/G | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149585448 | TACATGCTTCCATAC[-/G]AATGGATCTCAAAAT | 389337 |
rs112862686 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149609080 | ATCCCAGCTACTCAG[A/G]AGGCTGAGGCAGAGA | 389337 |
rs112865436 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | ARHGEF37 | GRCh38.p7 | 5:149595640 | TGGTACTCACTCACA[A/G]GGGCATTCTTATATT | 389337 |
rs112881076 | snp | A/G | 0.000331175 | 0.0128638 | synonymous-codon, upstream-variant-2KB | CSNK1A1, ARHGEF37 | GRCh38.p7 | 5:149550884 | ATAGATGTCCCCGAA[A/G]GAGCCAGACCCGATC | 389337 |
rs112953858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149599958 | TCTTATGTCACTTAA[C/T]ACCAGGGATATGTTT | 389337 |
rs113089720 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149586515 | TGATCCACCTGCCTC[A/G]GCCTCCCGAAGTGCC | 389337 |
rs113133780 | snp | A/G | 0.235273 | 0.249566 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149570999 | CCAGGCTGGAGTGCA[A/G]TAGCACAATCTTGCC | 389337 |
rs113160397 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149604177 | TGCCTTTGTGCTGGA[A/G]CCACAGAGCCAAAAT | 389337 |
rs113167962 | snp | A/G | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149559198 | TGGTGGCACATGCCT[A/G]TAATCCCAGCTACTC | 389337 |
rs113190610 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | CSNK1A1, ARHGEF37 | GRCh38.p7 | 5:149553479 | TGAGTTTTCCAGAGA[C/T]CACTCCTTTTCTGCT | 389337 |
rs113214526 | snp | A/G | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149560404 | CAGGCGTGAGCCACC[A/G]CACCTGGCCTATATT | 389337 |
rs113220339 | in-del | -/A | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149554975 | TCTATACTAAAAAGT[-/A]CAAAAATTAGCCGGG | 389337 |
rs113232618 | snp | C/T | 0.360842 | 0.224085 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149570571 | ACAAGTGCGAAACTC[C/T]GCCTCAAAAAAAAAA | 389337 |
rs113246631 | snp | C/T | 0.208779 | 0.246578 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149625180 | AAAGTGTTGGAATTA[C/T]AGGCGTGAGCCACCA | 389337 |
rs113257120 | snp | A/G | | | stop-gained | ARHGEF37 | GRCh38.p7 | 5:149627255 | CAACAGCGGCCGCTG[A/G]CTGGTGGACACCGGG | 389337 |
rs113260432 | snp | A/C | 0.5 | 0 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | CSNK1A1, ARHGEF37 | GRCh38.p7 | 5:149550268 | CATTAGCAAAACTCC[A/C]AGTCGCGACTACAAG | 389337 |
rs113261791 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149560130 | TTTTTTGTTTGTTGT[C/T]TTGAGACAGATTTTC | 389337 |
rs113287886 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149563016 | GGGTCTGACTTCCAG[C/T]TGTGCCTGAATTCCC | 389337 |
rs113298655 | snp | A/G | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149562698 | TGATCCGCCCGCCTC[A/G]GCCTCCCAAAGCGCT | 389337 |
rs113304542 | in-del | -/A | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149560766 | TTTGTACTTTCAAAG[-/A]AAAAAAAAAATTGTG | 389337 |
rs113311207 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | ARHGEF37 | GRCh38.p7 | 5:149580385 | TTTCTCTTCTGCAAG[A/C]TATACCACCCCTCTC | 389337 |
rs113313228 | snp | A/G | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149599418 | GCTCGGCTCACCCAG[A/G]AAAGCCCAAGGCAAA | 389337 |
rs113360391 | snp | C/T | 0.444444 | 0.157135 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149588518 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGGCCTCA | 389337 |
rs113403067 | in-del | -/C | 0.0422008 | 0.138995 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149615915 | AACAAAACAAAAAAA[-/C]ACGAACATTTCTTTA | 389337 |
rs113450059 | snp | G/T | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149565863 | TTTTTTTTTTTTTTT[G/T]TGTGAGACAGAGTTT | 389337 |
rs113454050 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | CSNK1A1, ARHGEF37 | GRCh38.p7 | 5:149551732 | TATTGGGAGGAGTCA[C/T]CTTCATGTTTCGTGG | 389337 |
rs113486514 | in-del | -/A | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149591227 | TTTGTGTTCCATCTC[-/A]AAAAAAAAAAAAAAG | 389337 |
rs113504247 | snp | G/T | 0.444444 | 0.157135 | utr-variant-3-prime | ARHGEF37 | GRCh38.p7 | 5:149633963 | TCTGATAAAAATAGA[G/T]AGCATAGGGGAACAG | 389337 |
rs113514672 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149558384 | GTGGCTTGCGCCTAT[-/A]AATCCCAGCTACTCA | 389337 |
rs113530399 | snp | A/C | 0.5 | 0 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | CSNK1A1, ARHGEF37 | GRCh38.p7 | 5:149550279 | CTCCAAGTCGCGACT[A/C]CAAGAAGAAGTGAAA | 389337 |
rs113550991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149619955 | TCACACGCCTGTAGT[C/T]CCAGCTACTCAGGAG | 389337 |
rs113582621 | snp | C/T | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149604200 | GCCAAAATGTTACTT[C/T]GTCTCCTGATCACAC | 389337 |
rs113585803 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | ARHGEF37 | GRCh38.p7 | 5:149595370 | TTTTTCTGTAGAGAC[A/G]AAATCTCACTATGTT | 389337 |
rs113637798 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149599932 | TATAGGCATTAAACA[A/G]GCAAATACAGTCTTA | 389337 |
rs113644804 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149556012 | AAGCCACAGTGTTTA[C/T]TCAAGCAACGGTCAC | 389337 |
rs113688594 | snp | C/G/T | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149613580 | TTGATTTCTTGACCT[C/G/T]GTGATCTGCCAGTCT | 389337 |
rs113701154 | in-del | -/T | 0.5 | 0 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149590594 | CTGGCTATTTTATTC[-/T]TTTTTTTTTTTTTGA | 389337 |
rs113746217 | snp | A/C | 0.233235 | 0.249437 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149570459 | TGGGCACCTGTAATC[A/C]CAGCTACTCAGGAGG | 389337 |
rs113997100 | snp | A/G | 0.067449 | 0.170807 | missense | ARHGEF37 | GRCh38.p7 | 5:149624063 | AAGCTGGTGGAGGAC[A/G]CACTGGGCCGGACGA | 389337 |
rs114028764 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149602516 | TTTTTGAGACGGGAT[C/T]TCACTCTGTTGCCCA | 389337 |
rs114104016 | snp | A/G | 0.0460142 | 0.144533 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149613177 | GTTTGTTTTAAATAT[A/G]AAAGCAACATATGCT | 389337 |
rs114169194 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149613715 | GCTTAACCATAGTAA[C/T]GAATATCTTTTCAGG | 389337 |
rs114184400 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149630912 | AAAAAACCTAAGCAG[C/G]CTGCATTTATTGAGC | 389337 |
rs114280886 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149591595 | GAGTATTGCAAAGAT[A/G]GTGAATAACTTAAGC | 389337 |
rs114329201 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149564109 | AAACATGCACCAACA[C/T]GCCTGGCTAATTTTT | 389337 |
rs114405232 | snp | A/G | 0.00755907 | 0.0610114 | upstream-variant-2KB, intron-variant | CSNK1A1, ARHGEF37 | GRCh38.p7 | 5:149553068 | TGGTGACTCTAAAGC[A/G]TGTTTTGACTAAGTT | 389337 |
rs114437259 | snp | G/T | 0.0528381 | 0.153711 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149598867 | ACACACATTCATATA[G/T]AGAGAGATCCCTCAA | 389337 |
rs114446240 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149600604 | CCCCACTGAGTACTC[C/T]GTCTGTTCCTCTCTT | 389337 |
rs114450475 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149623859 | TCCTAGGTTGTCTGA[C/T]GAAAATGCAAGAGAT | 389337 |
rs114622022 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149565384 | AATAAGTATTTAGTA[A/G]ATATTTTGTGGCTTA | 389337 |
rs114622478 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149572612 | CCTGATAGTTGGTCA[A/G]ACATTATTCTGGATG | 389337 |
rs114633040 | snp | A/C | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149612873 | TTCCTTGGGATTCCA[A/C]AATGCACGCTGACCC | 389337 |
rs114656027 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149613187 | AATATAAAAGCAACA[C/T]ATGCTTATTGAACAA | 389337 |
rs114734261 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149594394 | CAAATCAGCAGATCA[C/T]GGGGTGTGTTTGGGA | 389337 |
rs114737832 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149572597 | GCTGGGCCTCAGTGT[C/T]CTGATAGTTGGTCAA | 389337 |
rs114779826 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149602634 | ATAGTCTTCTTATTC[C/T]GAAATGGTTAGGATG | 389337 |
rs114804244 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149616303 | TAGTCAGTCGTGTCT[A/G]CTGTGGAGAGGCCGA | 389337 |
rs114935288 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149598959 | CAGGAGGCACCAGCT[A/G]TCTTGGGAATCACCT | 389337 |
rs115083592 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149630529 | GTGCTTGTGCCACAC[A/C]CACCGGGAAGGCTGT | 389337 |
rs115126523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149630240 | AAGGGATTTGGCTTT[A/G]CAGGGATGGAGTCCA | 389337 |
rs115256047 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149624299 | TTCTATTTGAGCTGG[A/G]GTGGGGGGACACACC | 389337 |
rs115276713 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149622666 | AGTTCAGCTCCAGGG[C/T]CTGGACTCTGAACCA | 389337 |
rs115354481 | snp | C/T | 0.0119091 | 0.0762411 | utr-variant-3-prime | ARHGEF37 | GRCh38.p7 | 5:149633322 | TGCTGCCCTCCCCCA[C/T]GCCCATGCCTGTGGC | 389337 |
rs115410606 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149611087 | GTCTCTCCTCTTCCC[A/G]CCTGCTAGCTTATTC | 389337 |
rs115658620 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149588611 | CCCCTTTATTCTTCA[A/G]CAGGGTCCTTTGCTC | 389337 |
rs115722204 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149613097 | CAATTCCAGAATGAT[A/G]GCTGAGGCAGCAGAG | 389337 |
rs115880218 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | ARHGEF37 | GRCh38.p7 | 5:149595008 | CATTTACATGAATTT[C/T]GGGAAAGGACACAAT | 389337 |
rs115881571 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149627701 | TGAGGGGAGCGATCA[C/T]CCTGCCCACTCCATA | 389337 |
rs115885998 | snp | A/G | 0.0528381 | 0.153711 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149609844 | GATAGGGCAGGCTGT[A/G]CCACAGAGACAAACA | 389337 |
rs115908541 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149628587 | CTGATCAAAGGGAGT[C/T]GTCTGTCCGGTAGGG | 389337 |
rs115971653 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149553565 | ATAAGGGGATGAGGT[A/G]TACATTTAGACGGAT | 389337 |
rs116032044 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149575883 | ACCCCCTGCCGTCCC[C/T]CCCCTCAAAAAATAC | 389337 |
rs116148001 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149614812 | TGGCTGATCTTTCCT[A/G]GACATTTGGTCTGGA | 389337 |
rs116164467 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149597588 | AGCTGTTACCTGCCT[A/T]TCAATATTGTTCAGG | 389337 |
rs116301461 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149625419 | AAGAGTCAGAAGACA[G/T]CCCTGAGATTCCCCA | 389337 |
rs116318665 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149576240 | ACAAAGCGAGACTCC[A/G]TCTCAAAAGCAAACA | 389337 |
rs116320238 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149585308 | AAACTTCACTCCTAG[A/G]TCCAGCTTTATTGTA | 389337 |
rs116336153 | snp | A/G | 0.0524604 | 0.153226 | intron-variant | CSNK1A1 | GRCh38.p7 | 5:149549816 | AAAGATGACCTGCAC[A/G]CATAACTGCAAATGA | 389337 |
rs116346415 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149629553 | CTCTGCAGAAAAGGC[A/C]CAGTGACAGGAGAGG | 389337 |
rs116373268 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149594262 | GTATTTCTCATGATT[G/T]TATTTATTTAGCAAC | 389337 |
rs116376668 | snp | C/T | 0.0948562 | 0.196037 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149570129 | TAGTCACGGATGATA[C/T]GATTTTGTACATAGG | 389337 |
rs116647383 | snp | C/T | 0.0136677 | 0.0815293 | missense, utr-variant-5-prime | ARHGEF37 | GRCh38.p7 | 5:149609653 | CGTACCGGAAGGAGC[C/T]GGAGCTGCAGCGGCA | 389337 |
rs116713274 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149601534 | ATTCATTCATCCAAC[A/G]GTTATTTAATGAGCA | 389337 |
rs116768476 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149618816 | TCAGCTTTGGGGTTG[C/T]GAGAACCAGCTCTGG | 389337 |
rs116822708 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149612923 | ATGTTCATTCTGTCT[C/T]TTAAGGCAACTCTTC | 389337 |
rs116892354 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149627619 | GGACCACCCTGAAAG[A/G]TGGAGATGGGCACGG | 389337 |
rs116900051 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149601645 | GAAGATAGACAAACA[A/G]CAGAATTGTAGGTAA | 389337 |
rs116954767 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149569124 | TGTTTGGATGTGACA[C/T]AGTTTATCCTTTATA | 389337 |
rs117068986 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149553576 | AGGTATACATTTAGA[C/T]GGATATTTTGGTATT | 389337 |
rs117311236 | snp | A/G | 0.084728 | 0.187577 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149588816 | AGCCTTGGGCAGCTA[A/G]CTGATGGATCCTCAA | 389337 |
rs117354494 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149610418 | TAGAGAATATGTATT[C/T]GAATTTAAATTTTCG | 389337 |
rs117363452 | snp | A/G | 0.0941369 | 0.195465 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149558640 | GGATTACAGGCGTGA[A/G]CCACTGTGCCCAACC | 389337 |
rs117491683 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | CSNK1A1, ARHGEF37 | GRCh38.p7 | 5:149550547 | GAATCACTGAAAGAG[A/G]ATTTTGCCGTTTCCA | 389337 |
rs117735101 | snp | C/T | 0.093777 | 0.195178 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149560272 | AAGCATGCGCCACCA[C/T]GCCCGACTAATTTTG | 389337 |
rs117898621 | snp | C/T | 0.121717 | 0.214577 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149575769 | TCACTGCAACCTCTG[C/T]CTCCCGGGTTCAAGC | 389337 |
rs118002514 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149610164 | TCCTACCACATGTCC[A/G]GGGTTGGAGAAGCGG | 389337 |
rs118041962 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149606381 | TAGGCCCTGGGACTG[C/T]GATCTCCCCATGGGG | 389337 |
rs118080436 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149617295 | TGAGCTAAAGTGAGA[C/T]CAATCTCATCCAAAC | 389337 |
rs118122026 | snp | G/T | 0.093777 | 0.195178 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149559032 | CATTTCTTAAAATTT[G/T]CAAAAACTGGCCAGG | 389337 |
rs118134326 | snp | C/T | 0.109461 | 0.206758 | intron-variant, upstream-variant-2KB | ARHGEF37 | GRCh38.p7 | 5:149595285 | GGCTCAAGCAATCCT[C/T]CTACCTTGGCCTCCT | 389337 |
rs137862998 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149610087 | ATATTAATCACTTCT[C/T]GTAATTCATTGGCCA | 389337 |
rs137884121 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149567499 | TTTCACTGTGGCATC[C/T]GTTAAGGTTTTTCTA | 389337 |
rs137930114 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149572936 | TTATTTTAAAAAAAA[A/T]TTTATTTAGCTCACA | 389337 |
rs138084389 | snp | A/C | 0.0115144 | 0.0749975 | utr-variant-3-prime | ARHGEF37 | GRCh38.p7 | 5:149633998 | TGAAATAGGAAACCC[A/C]CTCGTGGGTTCCACA | 389337 |
rs138125161 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149557091 | TAGGTCTGTGCAAAA[A/G]TACCCCAAAGTCTGA | 389337 |
rs138154884 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149597529 | CTCCCAAAGTGCTGG[A/G]ATTACAGGCATGAGC | 389337 |
rs138202624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149583949 | ACTTTTTGTAGACAC[A/G]GGGTCTTGCTATATT | 389337 |
rs138262764 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149624634 | CAAAAATTAGCTGAG[C/T]GTGGTGGTGTGCACC | 389337 |
rs138300807 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149628175 | ATTCCAGCTCCACCA[C/T]TTTGCTGACTGTGTG | 389337 |
rs138449633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149614546 | ATCTCTTCCAGGACC[C/T]CTTGCTCTCTAATTT | 389337 |
rs138480167 | snp | C/T | 8.27972e-05 | 0.00643364 | synonymous-codon | ARHGEF37 | GRCh38.p7 | 5:149619015 | TGAGCTGAAGAACAA[C/T]GTGGCTGCTTACCTG | 389337 |
rs138530354 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149604891 | TTTCGCCATGTTGGC[C/T]AGGCTGGTTGCAAAC | 389337 |
rs138534291 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149578118 | CCTGGCCTCCCACAG[C/T]GCCTGTCTATATTAC | 389337 |
rs138543916 | snp | C/T | 0.137527 | 0.223271 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149565912 | TAGAGTGCAATGGTG[C/T]GATCTCTGCTCACTG | 389337 |
rs138584965 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149609161 | CACACTCCAGCCTGG[A/G]GGACAAGAGCAAGAC | 389337 |
rs138691570 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149600597 | TTTTCTTCCCCACTG[A/C]GTACTCCGTCTGTTC | 389337 |
rs138794055 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149629479 | CTTTTTCTCAAACAG[A/G]AAGGGAGAGAGGGAA | 389337 |
rs138814111 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149588546 | TCATGTGATCTGCCC[A/G]CCTGACCTTCCAAAG | 389337 |
rs138818164 | snp | A/G | 0.00755907 | 0.0610114 | utr-variant-3-prime | ARHGEF37 | GRCh38.p7 | 5:149632540 | GGCCTGCCTGTGGGC[A/G]TGGGTCACACGGGAT | 389337 |
rs138830737 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149600803 | CACCACCATGCCGAG[A/C]TAATTTTTGTATTTT | 389337 |
rs138861945 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149591777 | ACTCTAGATATTGAA[A/C]ACTTTGTTATAAAAC | 389337 |
rs138919040 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149553873 | AAAATATTCTTGCTC[A/G]GTTAAAAGTTGAGCC | 389337 |
rs138935168 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149614156 | GAAGCATATTTGGGT[C/T]GTTTCCAATTATTTA | 389337 |
rs138957315 | snp | C/G | 0.0209421 | 0.100162 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149556433 | GCTCTTGTTGTCCAA[C/G]CTGGAGTGCAATGGT | 389337 |
rs139035564 | in-del | -/C | 0.124984 | 0.216497 | upstream-variant-2KB, intron-variant | ARHGEF37 | GRCh38.p7 | 5:149580303 | TGACCTCGTGATCTG[-/C]CCCCCCCTCAGCTTC | 389337 |
rs139064407 | snp | G/T | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149598779 | AGATATAGATATAGA[G/T]ATATAGATATAGATA | 389337 |
rs139066736 | snp | C/G/T | 0.00914312 | 0.0669923 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149558649 | GCGTGAGCCACTGTG[C/G/T]CCAACCAGACAACCC | 389337 |
rs139150439 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149593491 | ATTCATGTTGTAGAA[C/T]ATATGAATACAGTTG | 389337 |
rs139218907 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149578522 | TATCCACCCATTCAA[C/T]AAACACTTATTCAGC | 389337 |
rs139236546 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149576326 | ATGCAGGCTTTGAAG[A/T]CATACTTCTGAGGTT | 389337 |
rs139339830 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149569743 | GGCCTCAGCCTCCTA[A/C]CTGAGCAGCTGGGAT | 389337 |
rs139464820 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149554189 | AAAGTTGAAAGCTGC[A/G]TACGGTGGCTCATGC | 389337 |
rs139489230 | snp | A/T | 0.0111196 | 0.0737302 | utr-variant-3-prime | ARHGEF37 | GRCh38.p7 | 5:149634378 | ACAGCCTGTTCTGCC[A/T]GGTCTCAGAATGTAT | 389337 |
rs139499113 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149626985 | GGATCAGGCCCAGTA[C/G]TCCTGGCTGTCAAAA | 389337 |
rs139526604 | snp | A/G | 0.00706705 | 0.0590219 | missense | ARHGEF37 | GRCh38.p7 | 5:149621740 | CCCCACAGAAGCAAC[A/G]GCTAGAAGGCCTGGT | 389337 |
rs139538673 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149631070 | AGGTTAAATATTAGC[C/T]TAATACATGCCCTCC | 389337 |
rs139594630 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149629970 | GATTCCATTATGTGG[A/G]TGTCCAGAATGGGCA | 389337 |
rs139612027 | snp | C/G | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149614998 | GCTACTGGTCATAAT[C/G]AAGAAAAGACTGTGG | 389337 |
rs139614436 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149588761 | AAGAAAGGGAAAGAA[A/G]AAAAATTAAAAATAA | 389337 |
rs139751280 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149554209 | GTGGCTCATGCATGT[A/C]ATCCCAACACTTTGG | 389337 |
rs139751364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149606197 | CCGGCCTAGGTTTCA[C/T]GGCCACACCCAAGCT | 389337 |
rs139755881 | in-del | -/AAACAAAT | 0.122411 | 0.214991 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149609205 | AACAAAAAAACAAAA[-/AAACAAAT]AAACAAGCTAATGGT | 389337 |
rs139795760 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149601982 | GAGTTTGGAGTTTAT[C/T]CTAACTGTGATGGGG | 389337 |
rs139838252 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149606781 | TCAGATCATGTCACC[A/G]TTGCTCAAAGGCCTC | 389337 |
rs140006765 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149584428 | TGTTGCTGTCTTTCC[A/G]CCTCACTTCCAATCA | 389337 |
rs140139707 | in-del | -/ACACACACACAC | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149626242 | CATAGAGCATGGTGA[-/ACACACACACAC]ACACACACACACACA | 389337 |
rs140170130 | snp | A/T | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149599864 | CCAATGTAGATAATG[A/T]AGAAAGTGAAGTACT | 389337 |
rs140173472 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149585915 | AACCAAGAGTTGTGT[A/G]TGACCATATCAGTCT | 389337 |
rs140258826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149631568 | CTCAAACCATTAGAT[C/T]TGGAGAGGGAGAGGG | 389337 |
rs140295747 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149612880 | GGATTCCAAAATGCA[C/T]GCTGACCCCACCCTT | 389337 |
rs140315439 | snp | C/T | 0.108048 | 0.20579 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149615698 | AGATTGAGACCATCC[C/T]GGCCAACATGGTGAA | 389337 |
rs140347041 | snp | C/G | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149590244 | CTAGAATCAGAAGCA[C/G]TAGCTTGCTGCAGAA | 389337 |
rs140374859 | snp | G/T | 0.0228947 | 0.104514 | intron-variant, upstream-variant-2KB | ARHGEF37 | GRCh38.p7 | 5:149594566 | TTCAACAAATACTAA[G/T]ACATCCATAAGAACC | 389337 |
rs140459800 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | ARHGEF37 | GRCh38.p7 | 5:149635441 | TATTCTGAGGGCAGT[G/T]GGGGAGGCATGAAAG | 389337 |
rs140467350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149556286 | GCAACCTCCGCCTCC[C/T]GGGTGCAAGTGATTC | 389337 |
rs140543306 | in-del | -/A | 0.0861826 | 0.188849 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149586443 | TTTCTTTTAATTTTC[-/A]GTAGAGATGGGTTTT | 389337 |
rs140568405 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149631789 | TAGGACAGTGCCAGT[A/C]ACATAGTATGGGCTG | 389337 |
rs140622537 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149590502 | GGTCAGGCTGGTCTC[A/G]AACTCCTGACCTCGT | 389337 |
rs140623310 | snp | C/G | 0.0528381 | 0.153711 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149597402 | TAGCTGGGACTACAG[C/G]AGCCCGCCACCATGC | 389337 |
rs140643767 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149600214 | TTATAATCCTATGAG[A/G]TCACCCTGGTATATG | 389337 |
rs140690629 | snp | A/G | 0.0103295 | 0.0711199 | upstream-variant-2KB | CSNK1A1, ARHGEF37 | GRCh38.p7 | 5:149552034 | TCTTTCCACAGGAGG[A/G]GAAGAAAGAAAGAAG | 389337 |
rs140715807 | in-del | -/CACA | 0.295854 | 0.245759 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149625761 | ACCCTCCCACCTCTC[-/CACA]CACACACACACACAC | 389337 |
rs140760835 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149570176 | AAACACCTACTAAAG[C/T]TAATAAATGAATTTA | 389337 |
rs140788702 | in-del | -/CACACACG | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149626281 | ACACACACACACACA[-/CACACACG]CCTCTCTCAAGACAT | 389337 |
rs140799770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149575441 | GCTACATGGCTCTAT[A/G]CTCAGGGGACTGACC | 389337 |
rs140851754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149564459 | ATTTCTCCCGTTTAT[A/G]CATCTCAGGACTACA | 389337 |
rs140927716 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149577148 | TATAATCTTGGACAA[C/G]TTACTTAATCTTTCT | 389337 |
rs140960008 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149600524 | ACCCTTCAATGACAG[A/T]TGGGGAAACTGAGAG | 389337 |
rs140963767 | snp | C/T | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | ARHGEF37 | GRCh38.p7 | 5:149580843 | AAGGTTTGGTTGCCC[C/T]GATATGAAACTTTAC | 389337 |
rs141065542 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149596751 | ACAGGAGGGGGCATG[A/G]CAAGTGCAAAAGCAG | 389337 |
rs141075912 | snp | C/G | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149622802 | AGACTGGAGTTGATA[C/G]AAGAAAGAACACCCA | 389337 |
rs141113134 | in-del | -/TC | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149598749 | TCTCATATATATATA[-/TC]TATATATAGATATAG | 389337 |
rs141126764 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149577587 | CTCTGATTAGCTAAA[A/C]TTATAAAAGGTTGAG | 389337 |
rs141276477 | snp | C/T | 0.00597247 | 0.0543191 | utr-variant-3-prime | ARHGEF37 | GRCh38.p7 | 5:149633044 | GAATGGCTTGCTTTC[C/T]TGTTTCTGGTTAGAA | 389337 |
rs141328528 | snp | A/G | 0.00914312 | 0.0669923 | downstream-variant-500B | ARHGEF37 | GRCh38.p7 | 5:149635150 | ACAGAAAGAAATCAG[A/G]CAGATGAGGCCCGGT | 389337 |
rs141367264 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149593356 | GGCAATTGCCAATCT[G/T]TCTGTTTCTATCTGT | 389337 |
rs141368375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149604049 | GAATGGAAATTGATA[C/T]AGCCTCAGGCTGAAA | 389337 |
rs141460212 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149556639 | TGATCCACCTGCCTC[A/G]GCCTCCCAAAGTGCT | 389337 |
rs141515934 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149610869 | TAGATAACAAATCAC[C/T]CCCAAAATGTAGTGG | 389337 |
rs141518957 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149583552 | GGAATAGGAGTTGCT[A/G]GCAGTTGGCTCACAT | 389337 |
rs141530592 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149605505 | ATTTCAAGTGCCCAA[C/T]AGCCACGTGTGGCTG | 389337 |
rs141570963 | snp | A/G | 0.00355756 | 0.0420253 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149609534 | ACGACCCCTTGTTGC[A/G]TCTTCACTCTCAGGT | 389337 |
rs141644837 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149601859 | GTTTAAAGGACAGAC[A/G]GAAGGTTGATGTGGC | 389337 |
rs141875574 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149617791 | CCGGGAAGCGTGGCT[A/C]CCAGCTGGCCTGGCT | 389337 |
rs141900035 | snp | C/T | 0.106633 | 0.204807 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149588129 | GTCCTGAACTCCTGA[C/T]CCCGTGATCTGCCCG | 389337 |
rs141986307 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149592100 | TTCCCCAATGGTTAC[A/G]TCTTATTTAAATATA | 389337 |
rs142116296 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149626410 | TGGAAGCAGTATCAT[A/G]CAATGGAAAAACAGG | 389337 |
rs142268760 | snp | C/T | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149614878 | ATCATCAGGGAGGGC[C/T]CAGAGAAAGTTCCTG | 389337 |
rs142288450 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149600768 | CCTCAGCCTCCCGAG[C/T]AGCTGGGATTACAAG | 389337 |
rs142296894 | in-del | -/A | 0.490563 | 0.0680388 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149605227 | GCAAGACTGCATCTC[-/A]AAAAAAAAAAAAAAG | 389337 |
rs142306427 | snp | A/G | 0.0528381 | 0.153711 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149603036 | CTCCTAGGTTCAAGC[A/G]ATTCTCCTGCCTCAA | 389337 |
rs142321888 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149561478 | AAGAGTTACTGTGAA[A/G]TAATGCCGGAGGCTT | 389337 |
rs142337389 | in-del | -/A | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149610463 | TTATAAGATTAAAAA[-/A]CTTTAAAACATCAAA | 389337 |
rs142345063 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149555912 | GAGGATCGCTTGAGG[C/T]CAGGAGTTCAAGACC | 389337 |
rs142345893 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149567652 | AACCTGTTAACGTTT[A/G]TTTTCGTGGTTAAAT | 389337 |
rs142384852 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149574155 | GTGACAAGACCTTGA[A/G]ACTGTATTCCAAGGA | 389337 |
rs142462821 | snp | A/G | 0.0126979 | 0.078662 | utr-variant-5-prime, upstream-variant-2KB | CSNK1A1, ARHGEF37 | GRCh38.p7 | 5:149551354 | GTCACTCCGCGGACG[A/G]CGCCATCTTGTTACT | 389337 |
rs142481053 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149631748 | AATGATAGAATTATT[A/G]TGAGAACCCAAACCC | 389337 |
rs142569694 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149589656 | AGGTACCCGCCATCA[A/C]GCCTGACTAATTTTT | 389337 |
rs142575273 | snp | C/T | 0.00218579 | 0.0329866 | synonymous-codon | ARHGEF37 | GRCh38.p7 | 5:149624026 | GCTGCCCCACCACCA[C/T]GTCCCAGAGCCTGCC | 389337 |
rs142590133 | in-del | -/TCTT | 0.0509478 | 0.151255 | upstream-variant-2KB | CSNK1A1, ARHGEF37 | GRCh38.p7 | 5:149551825 | TTAACCTTTGATCTT[-/TCTT]CTGGCCGTTCCCCCG | 389337 |
rs142636078 | in-del | -/ATCTATATATAG | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149598748 | ATCTCATATATATAT[-/ATCTATATATAG]ATATAGATATAGATA | 389337 |
rs142637403 | snp | C/T | 0.107341 | 0.205301 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149625184 | TGTTGGAATTACAGG[C/T]GTGAGCCACCACACC | 389337 |
rs142656242 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149627342 | GCCGGTGCAGAGACC[C/T]GGGCACTCTTGTGGG | 389337 |
rs142756314 | snp | C/T | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149598458 | CCTCTTCTTTCTTCT[C/T]CCTCTTCTTTCTTTT | 389337 |
rs142784810 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ARHGEF37 | GRCh38.p7 | 5:149579498 | GTACCAGACTTTTCT[C/T]TGAAGCATCCCTAAT | 389337 |
rs142791834 | snp | C/G/T | 0.00248704 | 0.0351856 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149628777 | GACGGGAAGGTGGCC[C/G/T]GCAGCCTGCTAACCT | 389337 |
rs142802785 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149601048 | TCCTACTCTCAAAAG[C/T]CTGCAAATACATTCT | 389337 |
rs142825123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149553889 | GTTAAAAGTTGAGCC[C/T]GGGTGCAGTGGCTCA | 389337 |
rs142895418 | in-del | -/CTTT | 0.0138799 | 0.0821421 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149606854 | ACTGCACTCCACTTA[-/CTTT]AAGACCCTACATGAT | 389337 |
rs142975972 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149596482 | GCTAATTTTTGTATT[G/T]TGAGTAGAAATGCGG | 389337 |
rs143015181 | snp | C/G/T | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149617573 | CCTCTGAGGTTGGCC[C/G/T]TGTTAGCCCCATTTC | 389337 |
rs143060551 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149577173 | CTTTCTGAGCCTCAA[G/T]TTCATCATCTGTAAG | 389337 |
rs143127844 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149578601 | ATCAATAAGCTAACC[C/G]TGACAGTATACTTTT | 389337 |
rs143171773 | snp | A/G | 0.0944967 | 0.195752 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149570692 | ACCACCCTGGCCAAT[A/G]TGGTGAAACCCCGTC | 389337 |
rs143208714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149553835 | TTATAAAAAGGTGCC[A/G]ATGGTAGATGGTTTT | 389337 |
rs143209805 | snp | C/T | 0.00597247 | 0.0543191 | utr-variant-3-prime | ARHGEF37 | GRCh38.p7 | 5:149632911 | GGGTGTGTGAGGCTG[C/T]TGGCAGCAGGTGAAC | 389337 |
rs143331439 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149624538 | CAGCACTTTGGGAGG[C/T]CGAGGTGGGTGGATC | 389337 |
rs143335488 | in-del | -/TTCCA | | | utr-variant-3-prime | ARHGEF37 | GRCh38.p7 | 5:149632859 | CAAATTCAGAGGCTG[-/TTCCA]GGGAAGAGGGGATTT | 389337 |
rs143457583 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149615048 | TTGACTTGGGGACTC[C/T]GGATGAAATTCCAGA | 389337 |
rs143525611 | snp | C/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | ARHGEF37 | GRCh38.p7 | 5:149634012 | CACTCGTGGGTTCCA[C/G]AGATACCTACCGAAG | 389337 |
rs143628431 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149593678 | ATATGTATTATATAC[C/T]GTATTCTTAAAGTAA | 389337 |
rs143629030 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149598113 | CCCCAGTACTTCTTT[C/T]CCTTGGCCGTGCAAC | 389337 |
rs143730994 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149628144 | AGGCCCCCGAGGCCA[A/G]GAGGACTGGATTTGG | 389337 |
rs143738963 | snp | A/G | 0.00993419 | 0.0697739 | downstream-variant-500B | ARHGEF37 | GRCh38.p7 | 5:149635221 | CATCAATTACGTGCC[A/G]TGTAAGTGTCAGGAT | 389337 |
rs143821631 | in-del | -/C | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149601512 | CTTTAGTCTGTGTCT[-/C]TTTCACATTCATTCA | 389337 |
rs143875110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149599890 | GTACTTCTTTTATTT[C/T]ACCCTCCAGAAATTG | 389337 |
rs143919220 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149614723 | GATGACCAGCGTAGG[C/T]GTCTCCTGATGGGTA | 389337 |
rs143982029 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149557403 | GGGAATTTTCAAGGA[C/T]TTCCTGGAACTGCAG | 389337 |
rs143990240 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149574904 | TGTCTCTCCCTTGGC[C/T]GAATACTACAACTTC | 389337 |
rs144029303 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149578232 | AGAATCAGCTTTTGT[C/T]GCTTGCAACCATGGA | 389337 |
rs144088647 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149620982 | CAGGCTCTATGCTAA[A/G]CCCTTTATATTCCTT | 389337 |
rs144134621 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | ARHGEF37 | GRCh38.p7 | 5:149580353 | GCCGTGAGCCACCGC[A/G]CCCGGCACCCTTGGT | 389337 |
rs144154578 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149584648 | GGAGTCTCGCTCTGT[C/T]GCCCAGGCTGGAGTG | 389337 |
rs144245183 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149584270 | AGAACTGGGGAAATA[C/T]GGCTAAGGACAAACA | 389337 |
rs144275373 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ARHGEF37 | GRCh38.p7 | 5:149594964 | GATTGAATAAAGCCA[A/G]TCCTAAAAGATTACA | 389337 |
rs144300342 | snp | C/T | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149600265 | TGTTATTATGCAGTG[C/T]GTGACTGTATATGTT | 389337 |
rs144364535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149610432 | TCGAATTTAAATTTT[C/T]GAATGGGTAACGTGA | 389337 |
rs144478563 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | ARHGEF37 | GRCh38.p7 | 5:149635076 | ATCTTGTTTGCTCAG[G/T]TGTCCATTTAATGGA | 389337 |
rs144516331 | snp | C/T | 3.33689e-05 | 0.00408453 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149601083 | AACTCCCAACCACCT[C/T]TCATGGCTTCTTTGT | 389337 |
rs144560078 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149589493 | CCACCATGCCTGGCT[A/G]ATTTTTTGTTTTGTT | 389337 |
rs144564105 | in-del | -/AGAAG | 0.423413 | 0.180077 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149590185 | TGTGCCAGTGTGAAC[-/AGAAG]AGAAGAGAGAGAAAA | 389337 |
rs144591209 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149574227 | GACATTTTTCTCATG[A/C]AGTTTCTAGCAGAGG | 389337 |
rs144654314 | in-del | -/TTATTTATTTAT/TTATTTATTTATTTAT/TTATTTATTTATTTATTTAT/TTATTTATTTATTTATTTATTTAT | 0.395453 | 0.203331 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149599434 | AAGCCCAAGGCAAAC[lengthTooLong]TTATTTATTTATTTA | 389337 |
rs144692177 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149620300 | GAAGGGGATTCCAGC[A/G]TAAGATGGCCATGAC | 389337 |
rs144712098 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149578873 | CAACAAGTAGATTGC[C/T]GCTCTTCAAAATCTG | 389337 |
rs144813852 | in-del | -/TGTGTGTGTGTGTATA | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149558726 | GTGTGTGTGTGTGTG[-/TGTGTGTGTGTGTATA]TATATTTTTATATGT | 389337 |
rs144817225 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149574636 | TATATTGCCAGTCCA[A/C]ACTTCCCTCTCTCAG | 389337 |
rs144859136 | snp | C/T | 0.00279162 | 0.0372561 | utr-variant-3-prime | ARHGEF37 | GRCh38.p7 | 5:149634430 | GGGACCTGAACAAAA[C/T]TGGATGTCTTGTAGG | 389337 |
rs144905053 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | CSNK1A1 | GRCh38.p7 | 5:149549975 | ACCCAGGTAACTAAA[A/G]CACCAAGACCCGGAT | 389337 |
rs144941254 | snp | A/C/T | 0.00410292 | 0.045108 | missense, utr-variant-5-prime | ARHGEF37 | GRCh38.p7 | 5:149616569 | CCTTCTCCCTCAGGC[A/C/T]GCAAGCTGGATCTTC | 389337 |
rs145010060 | snp | A/G | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149629402 | AAAGTTAATAGCAGA[A/G]GTAAGTACCAGAGCC | 389337 |
rs145012904 | snp | C/G/T | 0.00433765 | 0.0463682 | synonymous-codon | ARHGEF37 | GRCh38.p7 | 5:149627267 | CTGGCTGGTGGACAC[C/G/T]GGGGGTACGTGAGCC | 389337 |
rs145030032 | snp | C/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | ARHGEF37 | GRCh38.p7 | 5:149632372 | AGTGCTTGGTGTGGT[C/G]GGGGCACAGGAGGCT | 389337 |
rs145080175 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149591765 | ATTCAATTAATTACT[C/G]TAGATATTGAACACT | 389337 |
rs145100857 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149596924 | AGCTACTAAAGTCTT[A/T]CAGCAGGGCACACCA | 389337 |
rs145105024 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149631235 | GGAGTGCAGTGCCAT[A/G]ATCTCGGCTTACTGC | 389337 |
rs145303517 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149613095 | TGCAATTCCAGAATG[A/T]TGGCTGAGGCAGCAG | 389337 |
rs145357626 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149590848 | AAGTGATCCTCCCGC[C/T]TCGTCCTCCCAAAGT | 389337 |
rs145393178 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149571774 | AAAAATAAAAAGTTA[A/G]CTGGGTATGGTGGTG | 389337 |
rs145420283 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149561378 | CTCTGTAAATCTCTT[C/T]TAGTCTGAAAAGTCC | 389337 |
rs145420596 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149611443 | GGCATCTAGCTCAGA[C/T]ATTTAATAAACACTG | 389337 |
rs145421808 | in-del | -/ACACACATCCT | 0.0471551 | 0.14613 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149622128 | GCAGCCCCATCAGCC[-/ACACACATCCT]AGCTGTGTGTAGGGG | 389337 |
rs145433052 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149576780 | GGCCAACATGGTGAA[A/G]ACCCATCTCTACTAA | 389337 |
rs145458927 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149569771 | GATTACAGGTGCGCA[C/T]CACCACGCCCGGCTA | 389337 |
rs145466373 | snp | A/G | 0.00194237 | 0.0311033 | missense | ARHGEF37 | GRCh38.p7 | 5:149621967 | TTTAACCAGCTGGTC[A/G]TGCAGTGGCTGGGCC | 389337 |
rs145468402 | snp | G/T | | | intron-variant, upstream-variant-2KB | ARHGEF37 | GRCh38.p7 | 5:149595510 | TAAAACATTATACAG[G/T]TCTGTATTTTTTGTC | 389337 |
rs145511480 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149582572 | CATAATATATGCTCA[A/G]TAAAAGTGCTGACGA | 389337 |
rs145619771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149576607 | TGTTATGTGATAAAT[A/G]TGTGAGCCACCACGC | 389337 |
rs145627608 | snp | C/T | 0.0554779 | 0.157039 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149592859 | ATCACAACCTCCGTC[C/T]CCTGGGTTCAAGCAA | 389337 |
rs145779259 | snp | G/T | 0.00716266 | 0.059414 | | | GRCh38.p7 | 5:149560679 | TGTAATCCCAACACT[G/T]TGGAGGGCGAGGGGG | 389337 |
rs145813180 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149627867 | TGAGGGGTGCCTGAG[A/G]TTATTGTCAGGGGAT | 389337 |
rs145965542 | in-del | -/ATTC/ATTCATTC/ATTCATTCATTC/CATT | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149629223 | AAGTGAGATTCATTC[lengthTooLong]ATTCATTCATTCATT | 389337 |
rs146043052 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149588721 | CCCCCTTCCTTAAAT[A/G]TTTAAATGGGCTCCT | 389337 |
rs146164695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149567658 | TTAACGTTTATTTTC[A/G]TGGTTAAATTATCCA | 389337 |
rs146177054 | snp | C/T | 0.126564 | 0.217402 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149558393 | CGCCTATAATCCCAG[C/T]TACTCAGGAGGCTGA | 389337 |
rs146200413 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149566218 | AAACCCTATGTGGGA[C/T]AGGCGAGGTGGTTCA | 389337 |
rs146258020 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149603222 | ACAGGTGTGAGCCAC[C/T]GTGCCTGGCCTAAAT | 389337 |
rs146282489 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149625055 | AGGCACCCACCACTA[C/T]GCCTGGCTAATTTTG | 389337 |
rs146406475 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149605772 | CATTTTACCAAAAAC[A/G]TCTCTGAGGCTCAGA | 389337 |
rs146434176 | in-del | -/TG | 0.0941369 | 0.195465 | upstream-variant-2KB, intron-variant | CSNK1A1, ARHGEF37 | GRCh38.p7 | 5:149552738 | AGCTATTCGGGAGTC[-/TG]AGAATCGCTTGAACC | 389337 |
rs146462587 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149576834 | GGTGGTGTACAACTA[C/T]AATCCCAGCTACTAG | 389337 |
rs146490419 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ARHGEF37 | GRCh38.p7 | 5:149580721 | TGACTACTACCAGCA[A/G]TAATAATAAATAATA | 389337 |
rs146588244 | snp | C/T | 0.0115144 | 0.0749975 | upstream-variant-2KB, intron-variant | CSNK1A1, ARHGEF37 | GRCh38.p7 | 5:149552447 | TTAGTAATAATAATG[C/T]TCACGAAAGAAAACT | 389337 |
rs146598186 | snp | C/T | 1.69507e-05 | 0.0029112 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149631967 | CATTTCTGTGTCACT[C/T]CCCATGTGTTTCAGG | 389337 |
rs146608199 | snp | A/G | 0.00517822 | 0.0506191 | downstream-variant-500B | ARHGEF37 | GRCh38.p7 | 5:149635116 | CGCCTCAGGGAGCTG[A/G]CCTGAGCTGCTGGGG | 389337 |
rs146610748 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149555163 | GAAAGAAAGAAAGGA[A/G]TCTTCAAAGAGCAAT | 389337 |
rs146780850 | in-del | -/CCTTGACTTC | 0.107341 | 0.205301 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149631681 | AATTTTGAGTAAGTT[-/CCTTGACTTC]CCTTGACTTCTCTGA | 389337 |
rs146814450 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | ARHGEF37 | GRCh38.p7 | 5:149635285 | GAGGCCTACCTCTGT[C/T]TCAGACTTGGCGGCC | 389337 |
rs146824997 | snp | A/G | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149597113 | TGGGATGGGGTGTAG[A/G]GGGACCACTGGGAGA | 389337 |
rs146891438 | snp | C/T | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149554200 | CTGCGTACGGTGGCT[C/T]ATGCATGTAATCCCA | 389337 |
rs146905806 | snp | A/G | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149587852 | GTAGCCAGGGTCCCT[A/G]TGTGCACATTCTTGT | 389337 |
rs147001365 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149556728 | GAGTTTCTCCGTGTT[A/G]ACCAGGCTGGTCTCA | 389337 |
rs147011219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149563229 | CTTCTGCCTCTTCCC[C/T]GTCAGATTCTAAAGC | 389337 |
rs147103860 | snp | C/T | 0.000698219 | 0.0186714 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149618162 | CGTGCTTCCCCTCTT[C/T]TCTGTCGTTGCAGCC | 389337 |
rs147126567 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149622850 | CTCTCAGATGTCAAC[A/G]TGAGAGCTGAATTGC | 389337 |
rs147145024 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149631445 | CAAAGTGCTGGGATT[A/G]TAGGCGTGAGCCACC | 389337 |
rs147174865 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149594056 | TTTGATACCTGTATA[C/T]AATGTGTAATGATCA | 389337 |
rs147259802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149614782 | TCCCACCTGCTCTGC[C/T]TATTCTTAGCTTCAT | 389337 |
rs147283331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149575281 | TTTCTTTACAGACTC[A/G]GTAGGAAAGGTCACC | 389337 |
rs147293960 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149578512 | CACACTCACTTATCC[A/G]CCCATTCAACAAACA | 389337 |
rs147387905 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149630814 | CTGCAGGACTTGCCC[A/G]GGATCATCCCAGCCC | 389337 |
rs147398805 | snp | A/G | 0.0941369 | 0.195465 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149554032 | AATTAGCCGGGCGTG[A/G]TGGCGCATGCCTGTA | 389337 |
rs147408463 | snp | C/T | 0.00279162 | 0.0372561 | utr-variant-3-prime | ARHGEF37 | GRCh38.p7 | 5:149633427 | ATTCTATGTAGCCAG[C/T]CTCTTTAACTTGGTA | 389337 |
rs147434697 | in-del | -/GGGGGGGG | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149617019 | TAGTAAGTTGTGGCT[-/GGGGGGGG]GTTCCAAGACTCACA | 389337 |
rs147492351 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149611170 | GTCTTAGCTGGGAAC[G/T]GGCACATTGTCATTC | 389337 |
rs147515945 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149614435 | AAAAGCTGCATAAAA[A/G]AGTATTGTCCAAATT | 389337 |
rs147567219 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149586661 | GGTGGAGGTTTAGAC[A/C]CAGATGGTCTCAGAG | 389337 |
rs147576863 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149589957 | CAGGCATGATCCACT[C/G]TGCCCAACCTACATC | 389337 |
rs147615867 | in-del | -/CAGTGG | 0.414741 | 0.188044 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149626956 | TCAGGGTGGGCCCTT[-/CAGTGG]CAGAGTTAGGATCAG | 389337 |
rs147671191 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149561466 | TAATCCTTGGCAAAG[A/G]GTTACTGTGAAATAA | 389337 |
rs147671672 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149611858 | ATATCCTGAAATATA[A/T]GTATAAATAAATATA | 389337 |
rs147681566 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149569777 | AGGTGCGCACCACCA[C/G]GCCCGGCTAATTTTT | 389337 |
rs147742218 | snp | C/T | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149631147 | CTTTCTTCCTTCCTT[C/T]TTTCCTTCCTTCCTT | 389337 |
rs147743302 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149622969 | CATCCAATTCTTTGC[A/T]TGAAAACTCTACTAA | 389337 |
rs147753170 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149627333 | CCCACAGAAGCCGGT[A/G]CAGAGACCCGGGCAC | 389337 |
rs147820026 | in-del | -/TTATTA | 0.122411 | 0.214991 | upstream-variant-2KB, intron-variant | ARHGEF37 | GRCh38.p7 | 5:149579574 | TCCAGGCAACTGATG[-/TTATTA]TTATTATTATTATTA | 389337 |
rs147847760 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149603800 | AATTAGCCAGATGTG[A/G]TGGCACACACTTGTA | 389337 |
rs147857598 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149608397 | TTTTTTTGAGATGGT[A/G]TCTTGCTCTGTTGTG | 389337 |
rs147902312 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149607505 | TTCATGGCACTTATC[A/G]TATGTGTATTGTCTC | 389337 |
rs147963615 | snp | C/T | 0.095934 | 0.196885 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149590369 | TCACAGCAACCTCTG[C/T]CTCCCGGGTTCAAGT | 389337 |
rs147981714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149613138 | GCAGATAACCTTCTT[C/T]GTTTTCCTTTATCAG | 389337 |
rs148003345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149601289 | GGAACTGTTCTCAGC[A/G]AGTGGTCACTGCTTA | 389337 |
rs148058583 | snp | C/T | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149598278 | CTCTTCTTCTTCTTC[C/T]TCTTCTTCTTCTTCT | 389337 |
rs148059767 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149563283 | CTACCCACCAGCCTT[C/T]CTACACCCTTCTTGC | 389337 |
rs148195924 | snp | C/T | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149577291 | AGCACCTGTTTTCAT[C/T]ATTACTATGGAAAGA | 389337 |
rs148266865 | snp | A/G | 0.00676609 | 0.0577691 | utr-variant-3-prime | ARHGEF37 | GRCh38.p7 | 5:149632998 | AACTCTGGGAAGGCG[A/G]TGATAAGGCCTGGTG | 389337 |
rs148344319 | snp | C/T | 0.0763149 | 0.179815 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149624539 | AGCACTTTGGGAGGC[C/T]GAGGTGGGTGGATCA | 389337 |
rs148405708 | in-del | -/TTAT | 0.11963 | 0.213316 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149585516 | ATAGTGCATACTGTA[-/TTAT]TTATTTATTTATTTA | 389337 |
rs148447133 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, utr-variant-5-prime | ARHGEF37 | GRCh38.p7 | 5:149589560 | GCTGGAATGCAGTGG[C/T]GAGATCTCAGCTCGC | 389337 |
rs148496730 | snp | A/G | 4.97442e-05 | 0.00498695 | missense, intron-variant | ARHGEF37 | GRCh38.p7 | 5:149620424 | CAGTGCAGTATTGCA[A/G]TTTGGCAAGAGACCT | 389337 |
rs148519671 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149578878 | AGTAGATTGCCGCTC[A/T]TCAAAATCTGTGTGA | 389337 |
rs148560976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149574689 | TGACACCTTCACTTG[C/T]ATAGCACAGGTATCA | 389337 |
rs148590242 | snp | C/G | 0.00835141 | 0.0640778 | utr-variant-3-prime | ARHGEF37 | GRCh38.p7 | 5:149634487 | TGGAACCAAGTCTAT[C/G]TCATGAAGGGAAAAT | 389337 |
rs148603059 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CSNK1A1, ARHGEF37 | GRCh38.p7 | 5:149550703 | GGACGAGGTTCGTAA[A/G]CCAGGAAAACTAGCT | 389337 |
rs148653749 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149625217 | GCCCCAAATGCTTTT[C/T]AAAAAATGTATTTTC | 389337 |
rs148792990 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149568537 | CACCCCTATCAAGAT[A/G]CAATACATTGGCCGC | 389337 |
rs148835263 | snp | C/T | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149582585 | CAATAAAAGTGCTGA[C/T]GATTATAGGGTGACT | 389337 |
rs148926461 | snp | A/G | 0.0256215 | 0.110247 | utr-variant-3-prime | ARHGEF37 | GRCh38.p7 | 5:149632897 | TACTGTGTTAGGTGG[A/G]GTGTGTGAGGCTGTT | 389337 |
rs148949264 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149560971 | ATACCAATAGATAGG[C/T]AGTTAGAAATTAGAA | 389337 |
rs148953672 | in-del | -/ATTA | 0.427727 | 0.175821 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149589323 | GACACATAATGTTTT[-/ATTA]ATTAATTAATTAATT | 389337 |
rs148979590 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149628043 | TGAGTCAATTAAAAA[A/C]TTAAGAAAGCGGTAC | 389337 |
rs148989545 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149587939 | TCTCACTCTGTCGCC[C/G]AGGCTGGAGTGCAGT | 389337 |
rs149096907 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149612521 | AATAACACCGTTGAA[A/G]TTGGGATTTATAAAA | 389337 |
rs149126376 | snp | C/T | 4.11497e-05 | 0.00453577 | synonymous-codon, intron-variant | ARHGEF37 | GRCh38.p7 | 5:149597886 | TGTCCGGGAGCTCAT[C/T]GACACTGAGGTCTCC | 389337 |
rs149170018 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149602988 | CCCAGGCTGGAGTGC[A/G]ATGGCATGATCTCGG | 389337 |
rs149178688 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149591379 | TGAGCCACCGTGCTC[A/G]GCCAGCCTTTGTCTT | 389337 |
rs149180151 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149555278 | AGAGATCACCTAGTT[C/G]AATAATAATAATTGT | 389337 |
rs149277530 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149566007 | GGCATGTGCCACCAC[A/G]CCTGGCTTTTTTATA | 389337 |
rs149295505 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149630248 | TGGCTTTGCAGGGAT[A/G]GAGTCCATGAGCGGG | 389337 |
rs149305235 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149589339 | ATTAATTAATTAATT[A/T]ATTTATAAGACAGGA | 389337 |
rs149329362 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149608617 | ACCTCGTGATCCACC[C/T]GTCTTGGCCTGCAAA | 389337 |
rs149337426 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149553726 | GAGGATGTGAGAAAA[G/T]TAAGCAATACATCTT | 389337 |
rs149358807 | snp | G/T | 0.0333695 | 0.124785 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149620246 | TCCCTCTCATTGGGG[G/T]TGTGTAGAGAGCCTG | 389337 |
rs149411418 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149614260 | ATTTCTAGGATGGGA[C/T]TGATGGAAGAAAGGG | 389337 |
rs149434707 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149574495 | CTTTCTTTGCCTGCC[C/G]CTTGGTTGTGTTCAC | 389337 |
rs149488363 | snp | A/G | 0.0528381 | 0.153711 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149604832 | GGATTACAGGCGTGC[A/G]CCACCACGCCCGGCT | 389337 |
rs149498007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149557373 | CTGCTGTTACACAAG[A/G]AACATAGATAAACTG | 389337 |
rs149642160 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149610396 | AGAAGCCTCAGGTAG[A/G]AAAATGTAGAGAATA | 389337 |
rs149661397 | snp | C/T | 0.0119091 | 0.0762411 | utr-variant-3-prime | ARHGEF37 | GRCh38.p7 | 5:149634409 | ATTTATTAAGTGCCA[C/T]TAAAAGGGACCTGAA | 389337 |
rs149665856 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149554193 | TTGAAAGCTGCGTAC[A/G]GTGGCTCATGCATGT | 389337 |
rs149683598 | snp | A/G/T | 0.000248486 | 0.0111439 | missense | ARHGEF37 | GRCh38.p7 | 5:149621898 | TACCAGGAGGAGGCC[A/G/T]CCCGGCACACATACC | 389337 |
rs149693228 | snp | C/T | 0.00517822 | 0.0506191 | upstream-variant-2KB, intron-variant | ARHGEF37 | GRCh38.p7 | 5:149581086 | GAGCTGGGGCAAGAA[C/T]CAAGGGCTCCTCGGC | 389337 |
rs149718412 | snp | A/C | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149583343 | GGTTTCACCGTGTTG[A/C]CCAGGCTGATTGCAA | 389337 |
rs149745660 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149576453 | ACACTTATCTTTTAG[G/T]ATCATCTAGCAGAAT | 389337 |
rs149821764 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149560473 | AAATTATCCCTTTAG[G/T]TGGGTATTTAAGGAC | 389337 |
rs149885521 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CSNK1A1 | GRCh38.p7 | 5:149549780 | AAAAAAGGCAGCAGC[C/T]AACCCTTCCGCGTAG | 389337 |
rs149958665 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149612413 | ACCTCGTGATCCGCC[A/C]ACCTCGGCCTCCCAG | 389337 |
rs150029696 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149631816 | GCTGTGGTACTAGCA[A/G]ATGCAGTCATTGCCT | 389337 |
rs150034141 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149602265 | TTTCACCGTATTGGT[C/T]AGACTTGTCTTGAAC | 389337 |
rs150079710 | in-del | -/G | 0.0298908 | 0.118541 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149606298 | GGGTGGTCATGTTCT[-/G]GTCTGGCTCTAGGGG | 389337 |
rs150127138 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149608750 | GCCTCAGGTTACACA[A/G]CTGGGGAAGGGTTGC | 389337 |
rs150137207 | snp | A/G/T | 0.00954224 | 0.0684493 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149564551 | CATCCTCGGCCGGGC[A/G/T]CGGTGGCTCCCGCCT | 389337 |
rs150186867 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149600546 | AACTGAGAGAAGCTA[A/G]CTGGCAGCAGACCTA | 389337 |
rs150209742 | snp | A/C | 0.0322114 | 0.122752 | upstream-variant-2KB, intron-variant | CSNK1A1, ARHGEF37 | GRCh38.p7 | 5:149553322 | GGAGAATCGCTTGAA[A/C]CTGGGAGGCAGAGGT | 389337 |
rs150240628 | snp | G/T | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149624900 | ACCAAATGCTTTTGG[G/T]TTTTTTTTTTTTTTT | 389337 |
rs150262890 | snp | A/C | 0.0333695 | 0.124785 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149627462 | GGACATGAAAAGCCA[A/C]CAAGAGGAATTGAGG | 389337 |
rs150344413 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149604556 | GCTTTTCTTCTCCTC[A/C]GTGCAACTGTGTGCC | 389337 |
rs150393350 | in-del | -/AA | | | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149571906 | TGAGACCCTGTCTCA[-/AA]AAAAAAAAAAAAAAA | 389337 |
rs150398371 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149556324 | TCAGCCTCTTGAGTG[G/T]CTGGGATTACAGGCA | 389337 |
rs150415980 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149624582 | AGTTCGAGACCAGCC[C/T]GGCCAACATGGCAAA | 389337 |
rs150495970 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149577924 | TGTAAAGTTTATTCA[G/T]TAAATTTTAGTGAAT | 389337 |
rs150515549 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149601902 | AGTGAGGGGAGACTG[C/T]TGGGGATAAAATAGA | 389337 |
rs150525669 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149554128 | AGCCGAGATTGTGCC[A/C]CTGCACTCCGGCCTG | 389337 |
rs150576612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149629848 | TTTGTACAATGGAAT[A/G]TTATTCAGCCATAGA | 389337 |
rs150598442 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149614951 | GGCTGAGATTTGAAA[C/T]CTTTGTGGCTTTCTC | 389337 |
rs150630705 | in-del | -/TTCCTTCCTTCT | 0.299158 | 0.245119 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149631137 | TTCTTTCTTTCTTTC[-/TTCCTTCCTTCT]TTCCTTCCTTCCTTC | 389337 |
rs150670326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149606607 | TCCGTCCACCCTCTG[C/T]AGGTAACTAATCTCA | 389337 |
rs150806348 | snp | C/T | 0.0383715 | 0.133092 | upstream-variant-2KB, intron-variant | ARHGEF37 | GRCh38.p7 | 5:149579770 | TATTTTTAGTAGAGA[C/T]GGGGTTTCAACATGT | 389337 |
rs150861568 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149583823 | CTGAGTGCAGTGATG[C/T]AGTCACAACTCACTG | 389337 |
rs150883577 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149569325 | TTATTTATTTATTTA[C/T]TTTTATTTTTGAGAT | 389337 |
rs150964736 | snp | A/T | 0.0185938 | 0.0946107 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149621432 | GACAGAGTGAGACCC[A/T]GTCTCAAAAAAAAAA | 389337 |
rs150986666 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ARHGEF37 | GRCh38.p7 | 5:149608565 | TTTAGTAAAGGCAGG[G/T]TTTTACCATGTTAGC | 389337 |