SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs476393 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:735182 | aaaaaaaatcattat[A/T]tgaaaaagatacatc | 7525 |
rs480645 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:771355 | ctggggaataagagc[A/C]aaactttgtctcaaa | 7525 |
rs489167 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:754713 | agagactcccaatcc[A/C]aaaaaaaaaaaaaaa | 7525 |
rs490678 | snp | G/T | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:773707 | AGTTGGAACAAAGTT[G/T]GCTAAAAGAAGTGGG | 7525 |
rs492056 | snp | C/T | 0.0126979 | 0.078662 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722894 | TCAGGAGATCGAGAC[C/T]ATCCTGGCTAACACG | 7525 |
rs492937 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:748988 | tttttagtagagacc[A/C]ggtttcaccatgttg | 7525 |
rs508143 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:744537 | ccaggcgtggtggca[A/T]gcacctgtaggctca | 7525 |
rs523762 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | YES1 | GRCh38.p7 | 18:761893 | agccATGATGTTAAC[A/G]TTTCTAAGACAACCC | 7525 |
rs532618 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:791866 | ttgagaacagcctga[C/G]caacatggtgaaacc | 7525 |
rs537141 | snp | A/G | 0.00532576 | 0.0513275 | synonymous-codon | YES1 | GRCh38.p7 | 18:724612 | GCTCCACTTGTTCTA[A/G]TACTTCACGGTTCAC | 7525 |
rs541436 | snp | C/T | 0.375 | 0.216506 | intron-variant | YES1 | GRCh38.p7 | 18:779909 | CAATGTATGTAGTCC[C/T]TTTTTTTTTTTTTTC | 7525 |
rs557308 | snp | A/C/G | 0.00438332 | 0.0466095 | downstream-variant-500B | YES1 | GRCh38.p7 | 18:721554 | aaaaaaaaacaaaac[A/C/G]aaacaaaaaaaaaAG | 7525 |
rs558535 | snp | G/T | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:743855 | gcagtggcgcaattt[G/T]ggctcactgcaacct | 7525 |
rs564942 | snp | A/G | 0.426507 | 0.177046 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722868 | GAGGCCGAGGCGGGC[A/G]GATCACAAGGTCAGG | 7525 |
rs572600 | snp | A/T | 0.0225045 | 0.103662 | intron-variant | YES1 | GRCh38.p7 | 18:774498 | ttaacatttatcgag[A/T]tggggaagattgcag | 7525 |
rs581987 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:771365 | ttttttttttttgga[A/G]acaaagtttggctct | 7525 |
rs605199 | snp | A/C | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:735812 | aagaactAGTTTCCC[A/C]AAAACTATTGAAAAA | 7525 |
rs631811 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:773719 | GAAACATAGGAAAGT[G/T]GGAACAAAGTTGGCT | 7525 |
rs642892 | snp | G/T | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:773549 | CTTTCCTCACTGTCT[G/T]ACCAGCCTTTTAATT | 7525 |
rs661509 | snp | A/C | | | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:775634 | agacctcatctctac[A/C]aaaagtaaaaaaatt | 7525 |
rs668277 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:744471 | ACCTGGGAGGTGGAA[A/G]TTGCAGTGAGCTGAG | 7525 |
rs681792 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:743831 | gcaacctctgcctcc[G/T]gggttcatgcgatcc | 7525 |
rs694301 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:793752 | GTTTTGTAAtatacc[A/C]aaaatagttataaag | 7525 |
rs1060910 | snp | A/G | 0.495095 | 0.0492773 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722830 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCC | 7525 |
rs1060922 | snp | A/G | 0.49917 | 0.0203505 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722402 | ATTCTGTGCCATGGC[A/G]TATATGTTCAAATTC | 7525 |
rs1061035 | snp | C/T | 0.234692 | 0.249531 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722118 | TTTATGTACTAAATC[C/T]AATCAGGAAAGTAAG | 7525 |
rs1274882 | snp | A/T | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:771032 | aaaaTCTGAAAAGTT[A/T]AAACCTAGAAAAACA | 7525 |
rs1274883 | snp | A/C | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:779006 | TTTAGATATACAAAC[A/C]ATTGACCTTAAAGTA | 7525 |
rs1275321 | snp | A/G | 0.230896 | 0.249269 | intron-variant | YES1 | GRCh38.p7 | 18:800088 | TCAAGTAGAATGCTT[A/G]TTTGAAATTCATCCT | 7525 |
rs1275322 | snp | C/G | 0.0225045 | 0.103662 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:813888 | GGGAGTCCAAGACAG[C/G]AGGATCACTTGAGTC | 7525 |
rs1290012 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:747448 | gggtcttggctctgt[C/T]gcccaggctagagtg | 7525 |
rs1298066 | snp | A/C | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:773764 | AATACAATCTGATCC[A/C]ATGCTGACTAATAAA | 7525 |
rs1298343 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:747418 | gcagtggcgtgatct[C/G]ggctcactgcaacct | 7525 |
rs1298706 | snp | A/T | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:752075 | TACAGAGTTTTATAA[A/T]TTGTAGAATACAGTA | 7525 |
rs1298709 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:744617 | agatcacttgaggtc[A/G]ggagtttgagaccag | 7525 |
rs1299123 | snp | A/C | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:773754 | ATTCACTTAAAATAC[A/C]ATCTGATCCCATGCT | 7525 |
rs1299134 | snp | G/T | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:783111 | tataGCCACTAGGTT[G/T]ggtggcacatgtctg | 7525 |
rs1299583 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:747383 | ctcccaggctcaagc[A/T]attctcctgcctcag | 7525 |
rs1547856 | snp | G/T | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:796971 | TAGAGCTAAATGACT[G/T]GTAAGACAAAACAAA | 7525 |
rs1547857 | snp | G/T | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:797101 | acatggaaaagtctt[G/T]gcaacataaagacaa | 7525 |
rs1630319 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:732436 | ttttttttttttttt[A/T]aaacacagtcttgct | 7525 |
rs1675153 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:777807 | gtgagactctggctt[A/T]aaaaaaaaaaaaaaa | 7525 |
rs1675154 | snp | A/C | | | downstream-variant-500B | YES1 | GRCh38.p7 | 18:721559 | AAAACAAAACAAAAC[A/C]AAAAAAAAAGAAAAT | 7525 |
rs1675157 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:761130 | CTTAAGCCTGAAGGC[A/C]AAATTGTAACAATCA | 7525 |
rs1784804 | snp | G/T | | | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:776163 | gatgatgtaaagcaa[G/T]ggtaattctcatgct | 7525 |
rs1784805 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:773823 | gggaaaaGTGTTTAA[A/G]GGAAGAGAGAGAGAG | 7525 |
rs1784806 | snp | A/C | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:734579 | aacaaaacaaaaaaa[A/C]CCAGGAGCAACTACA | 7525 |
rs1784807 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:734915 | gtaatcccagcgctt[G/T]gggaagccaaggcgt | 7525 |
rs1785227 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | YES1 | GRCh38.p7 | 18:789839 | ctgaggcaggcagat[C/T]gcctgaggtcagaag | 7525 |
rs1785228 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:790489 | TCCTCTTATTATAAC[A/G]AAAAATCTAGTATAG | 7525 |
rs1785231 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:751816 | TACCTTGGTCTTTTT[C/T]CCCTCTGATAGGTGG | 7525 |
rs1785232 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:738075 | AAAACAAAAATGGAT[G/T]GCCAACCTCCCCTAC | 7525 |
rs1785233 | snp | G/T | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:738178 | AAAGCTTTTCTGAAT[G/T]GTCAGATTCTGTGGA | 7525 |
rs1785585 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:728511 | atgctcaaaaagttt[G/T]ggattttggagcatt | 7525 |
rs1785586 | snp | G/T | | | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:775985 | tgtttccagtttttt[G/T]gctattagaataatg | 7525 |
rs1785590 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:744410 | agagtgagactccat[C/T]tccaaaaaaaaaaaa | 7525 |
rs1785591 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:785136 | tctgtgcataacttt[G/T]gggatatccgccacc | 7525 |
rs1940293 | snp | A/G | 0.387642 | 0.208697 | intron-variant | YES1 | GRCh38.p7 | 18:809504 | AGACCAGCCTGGCCA[A/G]CGTGGTGAAACCCCA | 7525 |
rs1940628 | snp | C/T | 0.48679 | 0.0801892 | intron-variant | YES1 | GRCh38.p7 | 18:785430 | CCAGCTTTACTTGTT[C/T]CTCTTTCTCCCCCCT | 7525 |
rs2305994 | snp | C/T | 0.242775 | 0.249896 | intron-variant | YES1 | GRCh38.p7 | 18:747825 | ACACACACAGAATTA[C/T]ATACCAGTCTTAATA | 7525 |
rs2846587 | snp | C/T | 0.389903 | 0.207189 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:813221 | CAGCTGGAATCGTGT[C/T]CGTCTGAATACACGC | 7525 |
rs2846831 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:810073 | GACTTATGCCCAAAC[A/C]ATTTTTTAAGTGATG | 7525 |
rs2846832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:807162 | acttttagtagagac[A/G]gggtttcaccatgtt | 7525 |
rs3214047 | snp | G/T | 0.203987 | 0.24574 | intron-variant | YES1 | GRCh38.p7 | 18:745884 | ATTTTGAGAAAGATA[G/T]AGTGAAAGTATTTAT | 7525 |
rs3786347 | snp | A/G | 0.492902 | 0.0591488 | intron-variant | YES1 | GRCh38.p7 | 18:743226 | TTAATCCACAGCTAA[A/G]CAATGACAGAAAACA | 7525 |
rs3786348 | snp | C/T | 0.491758 | 0.0636642 | intron-variant | YES1 | GRCh38.p7 | 18:743436 | TAAATGAATAAACTA[C/T]ACTGTAATATCAATT | 7525 |
rs3840903 | in-del | -/A | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:739919 | CAAAATTTAAAAAAA[-/A]TGAAAAGCTAAGAAG | 7525 |
rs3865403 | snp | A/T | 0.496583 | 0.0411924 | intron-variant | YES1 | GRCh38.p7 | 18:756085 | AAACTGTCTGAGCTT[A/T]AGGATTTTTCTTTTT | 7525 |
rs3865404 | snp | C/T | 0.472522 | 0.113946 | intron-variant | YES1 | GRCh38.p7 | 18:755862 | AAAAGCATCCTGATA[C/T]GGGACCCTTTACAAA | 7525 |
rs3865405 | snp | A/G | 0.455144 | 0.142885 | intron-variant | YES1 | GRCh38.p7 | 18:740876 | AAAAAAGATATTGGA[A/G]CATAAGAAATATAAT | 7525 |
rs3875086 | snp | C/T | 0.476314 | 0.106217 | intron-variant | YES1 | GRCh38.p7 | 18:798446 | TCTCCTTCTGACTTA[C/T]AGTGCA | 7525 |
rs3875087 | snp | C/T | 0.47614 | 0.106587 | intron-variant | YES1 | GRCh38.p7 | 18:798268 | AAGTTTCCTGAACTA[C/T]AGATTCATGACTTCT | 7525 |
rs3897601 | snp | A/G | 0.441568 | 0.160629 | intron-variant | YES1 | GRCh38.p7 | 18:767209 | ggctggagtacagtg[A/G]catgataatgggtca | 7525 |
rs3911636 | snp | A/C | 0.200801 | 0.245111 | intron-variant | YES1 | GRCh38.p7 | 18:746846 | TAGCCATTGGGGAAC[A/C]TAGTTGTAGGGTTTA | 7525 |
rs3911637 | snp | A/C | 0.243061 | 0.249904 | intron-variant | YES1 | GRCh38.p7 | 18:746779 | CAACTTTTAAAAAGT[A/C]AAAATTCACCTTCAG | 7525 |
rs3911638 | snp | C/T | 0.243061 | 0.249904 | intron-variant | YES1 | GRCh38.p7 | 18:746578 | GGTGCTTCTTACTTT[C/T]TGTTTTGTCCTTTTG | 7525 |
rs3915597 | snp | C/T | 0.15665 | 0.231917 | intron-variant | YES1 | GRCh38.p7 | 18:805318 | TTCTACATTTAGTTA[C/T]GTTTAAATACACAAA | 7525 |
rs3915598 | snp | A/G | 0.437965 | 0.164831 | intron-variant | YES1 | GRCh38.p7 | 18:805149 | gttcacataatgtca[A/G]aattgcctaatgagg | 7525 |
rs3915753 | snp | A/G | 0.437824 | 0.164991 | intron-variant | YES1 | GRCh38.p7 | 18:797195 | TTGCTCATAATCTTT[A/G]CCAGTTTTACTATTG | 7525 |
rs3915754 | snp | C/T | 0.436408 | 0.16659 | intron-variant | YES1 | GRCh38.p7 | 18:796757 | GAAGACTCTGTCTCA[C/T]AAAATAAATAAATAA | 7525 |
rs4084145 | snp | C/G | 0.00835062 | 0.0640748 | intron-variant | YES1 | GRCh38.p7 | 18:732812 | TTGCATTTTATAGCT[C/G]TTGGTTATCTCATGA | 7525 |
rs4084146 | snp | C/T | 0.466515 | 0.124985 | intron-variant | YES1 | GRCh38.p7 | 18:758487 | CACAGGGCATATGCA[C/T]TGGGGAAACAAGATT | 7525 |
rs4085840 | snp | A/G | 0.480144 | 0.097642 | intron-variant | YES1 | GRCh38.p7 | 18:804013 | AGAAACTAAAATTAC[A/G]GTGTTCTGAAAGTTT | 7525 |
rs4085841 | snp | A/C | 0.499872 | 0.0079862 | intron-variant | YES1 | GRCh38.p7 | 18:803838 | ATTTTCTGACTGATT[A/C]TCAGTTTTTGCCTGG | 7525 |
rs4085842 | snp | C/G | 0.499866 | 0.0081858 | intron-variant | YES1 | GRCh38.p7 | 18:803577 | CACCTGCTTGCTAGT[C/G]GCAGTGAAACCTGCC | 7525 |
rs4121508 | snp | A/G | 0.469937 | 0.118861 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:813553 | TTCTAGGAACTTAAG[A/G]AAATGCATATAAGGG | 7525 |
rs4121513 | snp | G/T | 0.499992 | 0.00199679 | intron-variant | YES1 | GRCh38.p7 | 18:809772 | CATGAATTTGTTGTT[G/T]TTTTTTTAAGGAATC | 7525 |
rs4121550 | snp | A/G | 0.499784 | 0.0103811 | intron-variant | YES1 | GRCh38.p7 | 18:784547 | gttcagaagtctgac[A/G]ccggtgtccctggac | 7525 |
rs4121551 | snp | C/G | 0.479744 | 0.0985793 | intron-variant | YES1 | GRCh38.p7 | 18:784612 | ctggagattcaaaga[C/G]aaaatcagttcttgc | 7525 |
rs4121552 | snp | A/G | 0.479824 | 0.098392 | intron-variant | YES1 | GRCh38.p7 | 18:800536 | TAAGCTAGTATTCCC[A/G]CTAGAAAACAATGTT | 7525 |
rs4369751 | snp | A/G | 0.46855 | 0.121392 | intron-variant | YES1 | GRCh38.p7 | 18:730329 | AGATTAGAACTGACC[A/G]AGGACCCAAGAGGAT | 7525 |
rs4474771 | snp | C/T | 0.237593 | 0.249692 | intron-variant | YES1 | GRCh38.p7 | 18:765688 | TAAATTGGCCGGGTG[C/T]GGTGGCTCACGCCTG | 7525 |
rs4520909 | snp | C/T | 0.44252 | 0.159487 | intron-variant | YES1 | GRCh38.p7 | 18:811699 | TGGGGGTCTGTGTAT[C/T]GGCCGACGCCGGTAG | 7525 |
rs4798578 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | YES1 | GRCh38.p7 | 18:779193 | aatcacttgagtcca[A/G]cagttcaggaccagc | 7525 |
rs5009288 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | YES1 | GRCh38.p7 | 18:808138 | TATATCCTGGTCTGC[A/G]TTGGGTTTACCTTTA | 7525 |
rs5822576 | in-del | -/A | 0.480382 | 0.097079 | intron-variant | YES1 | GRCh38.p7 | 18:749859 | GCAAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 7525 |
rs5822577 | in-del | -/G/GG | 0.492237 | 0.0618148 | intron-variant | YES1 | GRCh38.p7 | 18:756282 | TACAGTGGGGGGGGG[-/G/GG]CTCAATAACTATTTG | 7525 |
rs5822579 | in-del | -/T | 0.48378 | 0.0885831 | intron-variant | YES1 | GRCh38.p7 | 18:785154 | AGTTATGCACAGACC[-/T]TTTTTTTTTTTTAAC | 7525 |
rs5822580 | in-del | -/T | 0.499087 | 0.0213463 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:813659 | CGATGCTGTATTTTC[-/T]TTAGCTACTAAAACT | 7525 |
rs6506474 | snp | A/G | 0.46703 | 0.124089 | downstream-variant-500B | YES1 | GRCh38.p7 | 18:721198 | CTGGTATAATTTTAA[A/G]AAGAAGAAAATACTT | 7525 |
rs6506475 | snp | A/C | 0.46845 | 0.121572 | downstream-variant-500B | YES1 | GRCh38.p7 | 18:721459 | AGGAGAATGGCGTGA[A/C]CCCGGGAGGCGGAGC | 7525 |
rs6506476 | snp | A/G | 0.468148 | 0.122112 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:721698 | ATTCAGAATATATCA[A/G]TTTTTAAAAAACGAA | 7525 |
rs6506488 | snp | A/G | 0.450609 | 0.149185 | intron-variant | YES1 | GRCh38.p7 | 18:731694 | ATTTTGAggccaggc[A/G]cggtggctcacgcct | 7525 |
rs6506489 | snp | C/G | 0.49928 | 0.018956 | intron-variant | YES1 | GRCh38.p7 | 18:731794 | aacacggtgaaaccc[C/G]gtctctactaaaaat | 7525 |
rs6506511 | snp | C/T | 0.455024 | 0.143057 | intron-variant | YES1 | GRCh38.p7 | 18:750937 | AGTATGTCTGGGTAT[C/T]AGAGTTAGAAGAGGG | 7525 |
rs6506537 | snp | C/T | 0.451359 | 0.148171 | intron-variant | YES1 | GRCh38.p7 | 18:794272 | gcctcaaattcataa[C/T]ctaaatcaaatcatg | 7525 |
rs7226492 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | YES1 | GRCh38.p7 | 18:768239 | AAACCATGCATGAGG[G/T]Tctttgcatttccat | 7525 |
rs7227222 | snp | C/T | 0.499451 | 0.0165644 | intron-variant | YES1 | GRCh38.p7 | 18:763432 | aggtgtggcggctca[C/T]gtctgtaatctcagc | 7525 |
rs7227300 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:804926 | ctcaaaaaaaaaaaa[A/C]acaaaccaaaaaCCT | 7525 |
rs7227492 | snp | C/T | 0.381113 | 0.21286 | intron-variant | YES1 | GRCh38.p7 | 18:772063 | CATGGAATTTCACTC[C/T]TGTTGCCCAGGCTGG | 7525 |
rs7228015 | snp | A/G | 0.439918 | 0.162576 | intron-variant | YES1 | GRCh38.p7 | 18:770395 | CCCTCTGTGACCTCT[A/G]ATGTCTGTCAGTTCA | 7525 |
rs7228136 | snp | C/T | 0.469148 | 0.120308 | intron-variant | YES1 | GRCh38.p7 | 18:732017 | AAAGGGAAACACTTT[C/T]ATTTTTCCTCTTTAT | 7525 |
rs7228839 | snp | A/T | 0.15665 | 0.231917 | intron-variant | YES1 | GRCh38.p7 | 18:802973 | tggctcacacctgtt[A/T]tcccagcactttggg | 7525 |
rs7230203 | snp | A/G | 0.493881 | 0.054972 | intron-variant | YES1 | GRCh38.p7 | 18:735616 | ctactcgggaggctg[A/G]ggcaggagaatcgct | 7525 |
rs7230318 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:790698 | GGCTAACTAGGCaaa[A/T]aaaaattaataaaaa | 7525 |
rs7230710 | snp | A/T | 0.030665 | 0.119967 | intron-variant | YES1 | GRCh38.p7 | 18:810710 | TTTTAGCTAATGTCC[A/T]AAAATAAAAATACAA | 7525 |
rs7231360 | snp | A/G | 0.0547245 | 0.156101 | intron-variant | YES1 | GRCh38.p7 | 18:761890 | TATGGGTTGTCTTAG[A/G]AACGTTAACATCATg | 7525 |
rs7232858 | snp | C/T | 0.380333 | 0.213338 | intron-variant | YES1 | GRCh38.p7 | 18:773091 | GGTCTCCTAGATTGA[C/T]CTTGCTTTAATAGCT | 7525 |
rs7233153 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | YES1 | GRCh38.p7 | 18:803326 | AAATGTGATAATGCA[C/T]ATAAAAGTATGGCAT | 7525 |
rs7233166 | snp | C/T | 0.15665 | 0.231917 | intron-variant | YES1 | GRCh38.p7 | 18:803353 | GCATAGCACCTATCA[C/T]AGGACAGGCTTTCTT | 7525 |
rs7233932 | snp | C/G | 0.470327 | 0.118136 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:812712 | TGGAGCGCTCCGATT[C/G]TGCCCCTCTGCCTTT | 7525 |
rs7234709 | snp | A/G | 0.474723 | 0.109542 | intron-variant | YES1 | GRCh38.p7 | 18:736118 | gtcaaggctgcagtg[A/G]gctgaaatcacgcca | 7525 |
rs7235988 | snp | A/G | 0.103794 | 0.20279 | intron-variant | YES1 | GRCh38.p7 | 18:745322 | TAGGAAAGCTTATGC[A/G]ATCCAGCCCATGCAG | 7525 |
rs7236252 | snp | A/G | 0.498714 | 0.0253268 | intron-variant | YES1 | GRCh38.p7 | 18:732476 | aaCACCAATCACACT[A/G]CTGGGAAAGAACAGT | 7525 |
rs7236738 | snp | A/C | 0.0322114 | 0.122752 | intron-variant | YES1 | GRCh38.p7 | 18:808599 | ATGGAAGATCTTACT[A/C]AAACTTCCTGTAAAT | 7525 |
rs7237758 | snp | A/G | 0.478104 | 0.102316 | intron-variant | YES1 | GRCh38.p7 | 18:780321 | gatcatgaggactcc[A/G]cccttattaataaat | 7525 |
rs7240839 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:792554 | CTCTCTCtctCTCTC[C/T]CCCTCTGtatatgtg | 7525 |
rs7240974 | snp | A/G | 0.499382 | 0.017561 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:812421 | ACCGGAACTCGGGCC[A/G]CGCCGGCCCGGCTCC | 7525 |
rs7241258 | snp | C/T | 0.475877 | 0.107142 | intron-variant | YES1 | GRCh38.p7 | 18:769988 | gacggagtcttgctc[C/T]atcgcccagactggg | 7525 |
rs7241568 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | YES1 | GRCh38.p7 | 18:801417 | AATCCTCACTTCCTC[C/T]AGAAGTATAGCCTTG | 7525 |
rs7242129 | snp | C/T | 0.460925 | 0.134204 | intron-variant | YES1 | GRCh38.p7 | 18:780110 | gctgtggcacgcacc[C/T]gctacttgggaggat | 7525 |
rs7242400 | snp | C/T | 0.48692 | 0.0798058 | intron-variant | YES1 | GRCh38.p7 | 18:771861 | AAAAGTATTTCCTTA[C/T]GTATCTGCTTGGTAA | 7525 |
rs7242820 | snp | A/G | 0.331874 | 0.236213 | intron-variant | YES1 | GRCh38.p7 | 18:751066 | TAGAAGGATATGACC[A/G]TATTTTATGTTCCGG | 7525 |
rs7242861 | snp | A/C | 0.132409 | 0.220618 | intron-variant | YES1 | GRCh38.p7 | 18:731708 | cacggtggctcacgc[A/C]tgtaatcccagcatt | 7525 |
rs7243185 | snp | G/T | 0.47852 | 0.101384 | intron-variant | YES1 | GRCh38.p7 | 18:796460 | ACAGCATCAAGCTAT[G/T]TGGTATTGGCATAGA | 7525 |
rs7243499 | snp | A/C | 0.441295 | 0.160954 | intron-variant | YES1 | GRCh38.p7 | 18:770678 | cagggtgggtgggtg[A/C]ctgtaaagctcactt | 7525 |
rs7244065 | snp | A/T | 0.252421 | 0.249988 | intron-variant | YES1 | GRCh38.p7 | 18:728938 | atttcactgagttta[A/T]ttttcttgtttgagg | 7525 |
rs7244795 | snp | A/C | 0.472522 | 0.113946 | intron-variant | YES1 | GRCh38.p7 | 18:737869 | GGACTTAGGCATGCG[A/C]CACCACACCCAGCTA | 7525 |
rs7343001 | snp | A/C | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:740151 | CTGAATCAAGAATTC[A/C]GACAACTAGGAATAT | 7525 |
rs7343014 | snp | A/G | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:739966 | CCAAATAATTATCTA[A/G]GTCCTAGAAGAGGTC | 7525 |
rs7504637 | snp | C/G | 0.430285 | 0.173197 | intron-variant | YES1 | GRCh38.p7 | 18:765486 | TCAGTGCAACCTCCC[C/G]CTCCCCGGTTCAAGC | 7525 |
rs8084192 | snp | C/T | 0.330947 | 0.236533 | intron-variant | YES1 | GRCh38.p7 | 18:753630 | AGCTGGGATTACAGG[C/T]GTGCACCTCCACGCC | 7525 |
rs8085970 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | YES1 | GRCh38.p7 | 18:757332 | cacggtgaaaccccg[C/T]ctctactaaaaatgc | 7525 |
rs8087143 | snp | A/T | 0.498871 | 0.0237351 | intron-variant | YES1 | GRCh38.p7 | 18:738990 | caccacgcctggcta[A/T]ttttcagtattttta | 7525 |
rs8087495 | snp | A/G | 0.0655868 | 0.168795 | intron-variant | YES1 | GRCh38.p7 | 18:731962 | acagagcgagactcc[A/G]tttcaaaaaaaaaaa | 7525 |
rs8089002 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:793142 | cctcccgggttcaag[C/T]gatactcctgcctca | 7525 |
rs8089584 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | YES1 | GRCh38.p7 | 18:757346 | gcctctactaaaaat[A/G]caaaaaattagccgg | 7525 |
rs8090148 | snp | G/T | 0.475259 | 0.108435 | intron-variant | YES1 | GRCh38.p7 | 18:727654 | CTTGGTTTATTGTAT[G/T]TTACTCAAAATAAGT | 7525 |
rs8091095 | snp | C/T | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:747178 | AAACCTTAAAGAATG[C/T]AAGTCTTTGggccag | 7525 |
rs8091546 | snp | C/T | 0.499121 | 0.020948 | intron-variant | YES1 | GRCh38.p7 | 18:747464 | ACAGAGCCAAGACCC[C/T]GTCTCAAAAAAAAGA | 7525 |
rs8092146 | snp | G/T | 0.0581099 | 0.160244 | intron-variant | YES1 | GRCh38.p7 | 18:784403 | tatgtcacaaaacta[G/T]taagtgacagagcca | 7525 |
rs8092541 | snp | C/G | 0.441158 | 0.161117 | intron-variant | YES1 | GRCh38.p7 | 18:793171 | cagcctcccaagtag[C/G]tgggactacaggcgc | 7525 |
rs8092717 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | YES1 | GRCh38.p7 | 18:757340 | aaccccgcctctact[A/G]aaaatgcaaaaaatt | 7525 |
rs8093142 | snp | C/G | 0.452473 | 0.146644 | intron-variant | YES1 | GRCh38.p7 | 18:793547 | tcactaaattgctca[C/G]gctggtctcaaactc | 7525 |
rs8093439 | snp | A/G | 0.0314385 | 0.121371 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:812970 | TCCTTCCGAGGCAGG[A/G]ATCCTGTCCCTGCCC | 7525 |
rs8093865 | snp | G/T | 0.487049 | 0.0794222 | intron-variant | YES1 | GRCh38.p7 | 18:765919 | TAAGTTGAAGAATAA[G/T]AAGTGAGCCATGAAA | 7525 |
rs8094573 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | YES1 | GRCh38.p7 | 18:802959 | CAggctgggcatggt[A/G]gctcacacctgtttt | 7525 |
rs8094760 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | YES1 | GRCh38.p7 | 18:788670 | acgcctgtaatcccc[A/G]gcactttgggaggcc | 7525 |
rs8096858 | snp | C/T | 0.254944 | 0.249951 | intron-variant | YES1 | GRCh38.p7 | 18:761354 | CAGCATTAATTATTA[C/T]ATAAATTATACTTTG | 7525 |
rs8096895 | snp | A/C/G/T | 0.480236 | 0.215277 | intron-variant | YES1 | GRCh38.p7 | 18:757299 | acgaggtcaggagat[A/C/G/T]gagaccatcctggct | 7525 |
rs8098380 | snp | A/C | 0.466515 | 0.124985 | downstream-variant-500B | YES1 | GRCh38.p7 | 18:721563 | CAAAACAAAACAAAA[A/C]AAAAAGAAAATTGAC | 7525 |
rs8099748 | snp | C/G | 0.472709 | 0.11358 | intron-variant | YES1 | GRCh38.p7 | 18:744114 | ACTTAGTATGTTCCA[C/G]TATTGTGCTAAATTA | 7525 |
rs9635864 | snp | C/T | 0.243633 | 0.249919 | intron-variant | YES1 | GRCh38.p7 | 18:733474 | GCATTATGCTAATCA[C/T]TATGGAAACCTAAAA | 7525 |
rs9635865 | snp | C/T | 0.243633 | 0.249919 | intron-variant | YES1 | GRCh38.p7 | 18:733501 | AAAAAGCATGGCTTT[C/T]GGCCGGGCGCGGTGG | 7525 |
rs9635866 | snp | C/T | 0.243919 | 0.249926 | intron-variant | YES1 | GRCh38.p7 | 18:733643 | AAAAAATTAGCTGGG[C/T]GAGGTGGCAGGAGCC | 7525 |
rs9635867 | snp | A/G | 0.243633 | 0.249919 | intron-variant | YES1 | GRCh38.p7 | 18:734017 | ggcacagtggctcac[A/G]cctataatcccagca | 7525 |
rs9646493 | snp | G/T | 0.0437281 | 0.141251 | intron-variant | YES1 | GRCh38.p7 | 18:737083 | TAGAAGGAGATGATG[G/T]TAACAGGGTATAGTC | 7525 |
rs9675377 | snp | C/T | 0.156319 | 0.231784 | intron-variant | YES1 | GRCh38.p7 | 18:809383 | TAGCTCACCGCAATC[C/T]CTGTCTCCCGGGTTC | 7525 |
rs9944537 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | YES1 | GRCh38.p7 | 18:774297 | tttggtgatatcacc[C/T]agtcttatatcttta | 7525 |
rs9945217 | snp | C/T | 0.47517 | 0.10862 | intron-variant | YES1 | GRCh38.p7 | 18:774904 | actcctactactgtg[C/T]cccaacttgcctcac | 7525 |
rs9945303 | snp | A/G | 0.173643 | 0.238054 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:813556 | TAGGAACTTAAGGAA[A/G]TGCATATAAGGGTTT | 7525 |
rs9945495 | snp | A/T | 0.187369 | 0.242028 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:813787 | CACTAAATAGAGATA[A/T]TTTCGTCTTCCTAAA | 7525 |
rs9945719 | snp | C/G | 0.0513262 | 0.151752 | intron-variant | YES1 | GRCh38.p7 | 18:777790 | ccagcctggacaaca[C/G]agtgagactctggct | 7525 |
rs9945807 | snp | C/G | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:777882 | AGCATGTTTAGTAAA[C/G]CTATAACAAATTTGA | 7525 |
rs9946749 | snp | A/C | 0.0154597 | 0.0866004 | intron-variant | YES1 | GRCh38.p7 | 18:757313 | ttgagaccatcctgg[A/C]taacacggtgaaacc | 7525 |
rs9947493 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | YES1 | GRCh38.p7 | 18:731690 | CTTAATTTTGAggcc[A/G]ggcacggtggctcac | 7525 |
rs9947962 | snp | C/G | 0.499859 | 0.0083854 | intron-variant | YES1 | GRCh38.p7 | 18:805558 | AAATTGCAAAACTAA[C/G]GCCTAGGGAGTTTAC | 7525 |
rs9948030 | snp | C/T | 0.479663 | 0.0987666 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:775500 | gcttgtaaggcttct[C/T]ataaatggaatcacg | 7525 |
rs9948113 | snp | A/G | 0.185788 | 0.241613 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:814173 | GATTTCTTTTTTAGT[A/G]TATTCATCAATGTCA | 7525 |
rs9948497 | snp | C/T | 0.187053 | 0.241946 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:813923 | AGTTGGAGACCAGCC[C/T]GGGCAACATGGGAGA | 7525 |
rs9948550 | snp | A/G | 0.45946 | 0.136478 | intron-variant | YES1 | GRCh38.p7 | 18:786994 | TAGAACATAACTAGC[A/G]CAAATAATGAGAACT | 7525 |
rs9949560 | snp | C/T | 0.0584853 | 0.160693 | intron-variant | YES1 | GRCh38.p7 | 18:798232 | GAGATAAACTATGTG[C/T]TCTGTGTCACCTATT | 7525 |
rs9951100 | snp | C/T | 0.185472 | 0.241529 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:814148 | TTTTTTTTTTATTAC[C/T]ACATTCCCTGATTTC | 7525 |
rs9951960 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | YES1 | GRCh38.p7 | 18:794004 | gagctacacattcag[C/T]acacgtatcccagaa | 7525 |
rs9952321 | snp | A/G | 0.132409 | 0.220618 | intron-variant | YES1 | GRCh38.p7 | 18:809910 | cacttcagaagccag[A/G]tccctatcacaatct | 7525 |
rs9952902 | snp | A/T | 0.441295 | 0.160954 | intron-variant | YES1 | GRCh38.p7 | 18:792078 | TAAAAAAAATAGTGT[A/T]TTCTCAGTATGCAAG | 7525 |
rs9952996 | snp | C/T | 0.482384 | 0.0921818 | intron-variant | YES1 | GRCh38.p7 | 18:792172 | agccaagtgtggtgg[C/T]gcatgcctgtaatcc | 7525 |
rs9953536 | snp | C/T | 0.493568 | 0.0563433 | intron-variant | YES1 | GRCh38.p7 | 18:789653 | GAACTACAGCAAAGG[C/T]TGTATTCAGAGCAAA | 7525 |
rs9954727 | snp | A/G | 0.173965 | 0.238157 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:813621 | AAGGTAGGCGTAGGC[A/G]TTAAAGAGACACATA | 7525 |
rs9954735 | snp | G/T | 0.173965 | 0.238157 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:813629 | CGTAGGCGTTAAAGA[G/T]ACACATAATGTGGAA | 7525 |
rs9957428 | snp | A/T | 0.473081 | 0.112848 | intron-variant | YES1 | GRCh38.p7 | 18:734839 | cattcaatccagcaa[A/T]cccactactgggtat | 7525 |
rs9957772 | snp | C/T | 0.460813 | 0.134379 | intron-variant | YES1 | GRCh38.p7 | 18:781513 | CCTGCCCCCACACCA[C/T]TTATGACACTGAATT | 7525 |
rs9958334 | snp | A/G | 0.477684 | 0.103247 | intron-variant | YES1 | GRCh38.p7 | 18:789916 | tacaaaaaattagct[A/G]ggcatggtggcacat | 7525 |
rs9958540 | snp | A/G | 0.499831 | 0.00918375 | intron-variant | YES1 | GRCh38.p7 | 18:810514 | CAGCAAAACCTAACT[A/G]CGAAATTAAAGCCAT | 7525 |
rs9958583 | snp | A/G | 0.47743 | 0.103805 | intron-variant | YES1 | GRCh38.p7 | 18:782910 | ATATTAGCCACTCCT[A/G]ACCTGAAGTGATCCA | 7525 |
rs9959614 | snp | C/T | 0.132409 | 0.220618 | intron-variant | YES1 | GRCh38.p7 | 18:734122 | tgtctgtaccaaaaa[C/T]acaaaacttagccag | 7525 |
rs9960351 | snp | C/T | 0.132066 | 0.220435 | intron-variant | YES1 | GRCh38.p7 | 18:734888 | atcagccaggtgtgg[C/T]ggctcacgcctgtaa | 7525 |
rs9960806 | snp | C/T | 0.131038 | 0.219882 | intron-variant | YES1 | GRCh38.p7 | 18:779236 | aggagacccccgtcc[C/T]ggcaaaaaatttttt | 7525 |
rs9961091 | snp | C/G | 0.459914 | 0.13578 | intron-variant | YES1 | GRCh38.p7 | 18:787846 | AGTGTGGATAAAAAA[C/G]ACTGATATTAATCCA | 7525 |
rs9961702 | snp | A/G | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:811461 | CAAGAAGAAAAACAC[A/G]CTTTAAGACAATTTT | 7525 |
rs9961743 | snp | C/T | 0.472989 | 0.113031 | intron-variant | YES1 | GRCh38.p7 | 18:742858 | AAGTCTATATGCATA[C/T]AAATCAAGACTCTTA | 7525 |
rs9962212 | snp | C/T | 0.0581099 | 0.160244 | intron-variant | YES1 | GRCh38.p7 | 18:767426 | aaagtgatgggatta[C/T]agacataagccacaa | 7525 |
rs9962284 | snp | C/T | 0.441021 | 0.161279 | intron-variant | YES1 | GRCh38.p7 | 18:790345 | GGCGTCACTGAACTC[C/T]AGCCTCGGCAACAAG | 7525 |
rs9964147 | snp | C/T | 0.440746 | 0.161604 | intron-variant | YES1 | GRCh38.p7 | 18:783324 | ACTCAAACTAGTACA[C/T]CCTAAATGTCTTCTC | 7525 |
rs9964705 | snp | A/C | 0.454423 | 0.143914 | intron-variant | YES1 | GRCh38.p7 | 18:754415 | TCTCACTTATCAAAT[A/C]TCAGCTCAAggctgg | 7525 |
rs9965976 | snp | C/T | 0.0520825 | 0.152737 | intron-variant | YES1 | GRCh38.p7 | 18:791792 | aggcgtggtggctca[C/T]gtctgtaatcccagc | 7525 |
rs9966644 | snp | C/T | 0.185472 | 0.241529 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:814120 | ACTGAGTTTGCTTCT[C/T]TTCGCCCTCCCTTTT | 7525 |
rs9966850 | snp | A/G | 0.477937 | 0.102688 | intron-variant | YES1 | GRCh38.p7 | 18:790311 | AACCCGAGAGGCGGA[A/G]GTTGCAATGAGCCGA | 7525 |
rs9966897 | snp | A/C | 0.472522 | 0.113946 | intron-variant | YES1 | GRCh38.p7 | 18:737431 | GCACTCCAGCCTGGG[A/C]AACAGAGCGAGACTC | 7525 |
rs9967082 | snp | A/T | 0.0517044 | 0.152246 | intron-variant | YES1 | GRCh38.p7 | 18:790581 | AAAGGGAGAGTACAC[A/T]GTATTAGGTATGAGA | 7525 |
rs10164116 | snp | A/G | 0.0633504 | 0.166319 | intron-variant | YES1 | GRCh38.p7 | 18:736208 | aaCATTACAGATAGG[A/G]AGGCATTCCAGATGG | 7525 |
rs10460020 | snp | A/G | 0.466308 | 0.125343 | intron-variant | YES1 | GRCh38.p7 | 18:758443 | ACTTTATTTCCTACT[A/G]TCCTCATACTTACGC | 7525 |
rs10617278 | in-del | -/CCCC | | | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:812336 | TCCTCCGCCCCCCCC[-/CCCC]GGCCCCGCCCCCTGA | 7525 |
rs10645789 | in-del | -/TT | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:769958 | TCTTTTTTTTTTTTT[-/TT]GAGACGGAGTCTTGC | 7525 |
rs10853356 | snp | A/C | 0.460365 | 0.13508 | intron-variant | YES1 | GRCh38.p7 | 18:778383 | TCAACCTATGGCACA[A/C]TCTACTAACTTTGGA | 7525 |
rs11081309 | snp | G/T | 0.0197687 | 0.0974348 | intron-variant | YES1 | GRCh38.p7 | 18:730855 | GTTGCATGGCTGTGT[G/T]GTTTTTTTCTAGCCC | 7525 |
rs11081316 | snp | C/T | 0.498871 | 0.0237351 | intron-variant | YES1 | GRCh38.p7 | 18:742501 | GGGGAAAAAAGTTCC[C/T]AGAAGTCCTGAATAT | 7525 |
rs11081327 | snp | C/G | 0.199812 | 0.24491 | intron-variant | YES1 | GRCh38.p7 | 18:749136 | ACTGGACTCCAGCCT[C/G]GGCTACAGAGCGAGA | 7525 |
rs11081340 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | YES1 | GRCh38.p7 | 18:759886 | CACGACAAGCCCCGG[C/T]GTATGATGTTCCCCT | 7525 |
rs11081341 | snp | C/G | 0.226188 | 0.248863 | intron-variant | YES1 | GRCh38.p7 | 18:759899 | GGTGTATGATGTTCC[C/G]CTTCCTGTGTCCAAG | 7525 |
rs11081342 | snp | A/T | 0.499859 | 0.0083854 | intron-variant | YES1 | GRCh38.p7 | 18:760548 | GTGCACAGGTTATAT[A/T]CAAATACATGCCATT | 7525 |
rs11324966 | in-del | -/T | 0.454423 | 0.143914 | intron-variant | YES1 | GRCh38.p7 | 18:770269 | CCCGGCCCTTTTATC[-/T]TTTTTTTTTTTTTTT | 7525 |
rs11356301 | in-del | -/G | 0.468963 | 0.120644 | intron-variant | YES1 | GRCh38.p7 | 18:792861 | CTCAATAAAAGCCAA[-/G]GGGGGGGAAAAAGCT | 7525 |
rs11372019 | in-del | -/T/TT | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:748374 | CTTTTTTTTTTTTTT[-/T/TT]AAAGCTTTAAGGTGT | 7525 |
rs11382218 | in-del | -/A | 0.162253 | 0.234095 | intron-variant | YES1 | GRCh38.p7 | 18:809764 | GATTCCTTAAAAAAA[-/A]CAACAACAAATTCAT | 7525 |
rs11412031 | in-del | -/T | 0.460365 | 0.13508 | intron-variant | YES1 | GRCh38.p7 | 18:791083 | TGAAACCCCATCTCT[-/T]ATTAAAAATACAAAA | 7525 |
rs11432383 | in-del | -/T | | | intron-variant | YES1 | GRCh38.p7 | 18:744395 | TCTTTTTTTTTTTTT[-/T]GAGATGGAGTCTCAC | 7525 |
rs11460599 | in-del | -/A | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:732443 | AAAAAAAAAAAAAAA[-/A]AAAAACACCAATCAC | 7525 |
rs11548679 | snp | C/T | 0 | 0 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723778 | ACATTAATATTCATG[C/T]TCATGGAACTGAAAG | 7525 |
rs11659287 | snp | A/G | 0.0829062 | 0.185956 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722821 | ATGTAggctgggcgc[A/G]gtggctcacgcctgt | 7525 |
rs11660899 | snp | C/T | 0.460813 | 0.134379 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:776018 | agcaatgaacattcc[C/T]gagccctccttggta | 7525 |
rs11662461 | snp | A/G | 0.499137 | 0.0207489 | intron-variant | YES1 | GRCh38.p7 | 18:761127 | ATACTTAAGCCTGAA[A/G]GCAAAATTGTAACAA | 7525 |
rs11662984 | snp | C/T | 0.477768 | 0.103061 | intron-variant | YES1 | GRCh38.p7 | 18:778883 | AGCAAACAAAGAACT[C/T]CATTTTCCAAGAGTC | 7525 |
rs11663085 | snp | A/G | 0.105569 | 0.204058 | intron-variant | YES1 | GRCh38.p7 | 18:782897 | acagggtttcgccat[A/G]ttagccactcctaac | 7525 |
rs11664027 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:807367 | agccaggcatggtgg[G/T]gcacacctgtggtcc | 7525 |
rs11664175 | snp | C/T | 0.472989 | 0.113031 | intron-variant | YES1 | GRCh38.p7 | 18:760281 | ttgagaccagcctgg[C/T]caacatggtgaaacc | 7525 |
rs11664455 | snp | A/G | 0.106787 | 0.205446 | intron-variant | YES1 | GRCh38.p7 | 18:793667 | ACAAAAAAAGTAAGA[A/G]AATTAACTGAAAAGC | 7525 |
rs11664589 | snp | C/G | 0.475437 | 0.108066 | intron-variant | YES1 | GRCh38.p7 | 18:785964 | TCTCTCTCTCCCTCA[C/G]TCTAACCCTCTCTCA | 7525 |
rs11875644 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:789615 | ccccaaaacaaaaaa[A/C]CCCAACAACGTTCTA | 7525 |
rs11876666 | snp | A/G | 0.0584853 | 0.160693 | intron-variant | YES1 | GRCh38.p7 | 18:805638 | ATCTAGATAGTGTTA[A/G]TGCTCTACCTTCCAG | 7525 |
rs11876917 | snp | G/T | 0.0532157 | 0.154195 | intron-variant | YES1 | GRCh38.p7 | 18:765295 | atatatatatatatC[G/T]GTAGCAATTTTTTCA | 7525 |
rs11877582 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | YES1 | GRCh38.p7 | 18:771420 | ATTTCTTAAATGAAC[C/T]TGTGTTTAACTTTTT | 7525 |
rs12185416 | snp | C/T | 0.469346 | 0.119947 | intron-variant | YES1 | GRCh38.p7 | 18:729030 | tttttaaaaatgttg[C/T]tactgtttcattttt | 7525 |
rs12185420 | snp | C/T | 0.251859 | 0.249993 | intron-variant | YES1 | GRCh38.p7 | 18:729377 | ccaagatcgtgccac[C/T]gtactccagcctggg | 7525 |
rs12185469 | snp | A/C | 0.213635 | 0.247341 | intron-variant | YES1 | GRCh38.p7 | 18:731442 | GATAAAATTTGATGG[A/C]ATTAGATCTACAGCT | 7525 |
rs12185470 | snp | C/T | 0.228547 | 0.249078 | intron-variant | YES1 | GRCh38.p7 | 18:731456 | GCATTAGATCTACAG[C/T]TGGAGGGAACTGTAG | 7525 |
rs12185477 | snp | A/G | 0.251296 | 0.249997 | intron-variant | YES1 | GRCh38.p7 | 18:729370 | cagtgaaccaagatc[A/G]tgccactgtactcca | 7525 |
rs12232748 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | YES1 | GRCh38.p7 | 18:796883 | GTGAAAATAGATTTA[A/G]TAACTAGCAGTAGTG | 7525 |
rs12326411 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | YES1 | GRCh38.p7 | 18:728115 | acagggcaggcaaat[C/T]gcttgagcctaggat | 7525 |
rs12326724 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | YES1 | GRCh38.p7 | 18:727922 | TATATaggctgagta[A/T]cccttatctgaaatg | 7525 |
rs12327321 | snp | G/T | 0.0146672 | 0.084371 | intron-variant | YES1 | GRCh38.p7 | 18:728064 | ttatgagccaggcac[G/T]gtggctcgcacctgt | 7525 |
rs12327478 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | YES1 | GRCh38.p7 | 18:726147 | ACTTCACTCAAAggc[C/T]gggtgcggtggctca | 7525 |
rs12454861 | snp | C/G | 0.461923 | 0.132621 | intron-variant | YES1 | GRCh38.p7 | 18:771286 | gcatgagactcattt[C/G]aacctaggaggcgga | 7525 |
rs12456072 | snp | A/C | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:763957 | aaaacccgtttctac[A/C]aaaaatagaaaaaat | 7525 |
rs12456826 | snp | C/T | 0.5 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:771237 | ctgggcatggtggtg[C/T]atgcctgtaatccca | 7525 |
rs12458128 | snp | A/G | 0.441295 | 0.160954 | intron-variant | YES1 | GRCh38.p7 | 18:763918 | tgaggtcaggagatc[A/G]agaccatcctggcta | 7525 |
rs12604489 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:765584 | tttgtatttttagta[A/G]agacacggtttcacc | 7525 |
rs12607170 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:779365 | gttatgatcgcacca[C/G]tgcactccagcctcg | 7525 |
rs12607313 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | YES1 | GRCh38.p7 | 18:749959 | TTATAACACATAAGC[C/T]GTCATTTTTTCAAAA | 7525 |
rs12954187 | snp | C/T | 0.234692 | 0.249531 | intron-variant | YES1 | GRCh38.p7 | 18:744760 | GCTGTTCTTGAACTC[C/T]TGGCCTCAAGTGATC | 7525 |
rs12955086 | snp | A/C | 0.0748431 | 0.178382 | intron-variant | YES1 | GRCh38.p7 | 18:799585 | caaggtggtgcatgc[A/C]cgtaatgagcaactc | 7525 |
rs12955492 | snp | A/T | 0.42 | 0.183303 | intron-variant | YES1 | GRCh38.p7 | 18:781287 | aaaaaaaaaaaaaaa[A/T]aaGAGGGCCTTGTAT | 7525 |
rs12955537 | snp | A/C | 0.489608 | 0.0713316 | intron-variant | YES1 | GRCh38.p7 | 18:732458 | AAAAAAAAAAAAAAA[A/C]AAAACACCAATCACA | 7525 |
rs12955644 | snp | C/G | 0.332799 | 0.23589 | intron-variant | YES1 | GRCh38.p7 | 18:771046 | TAAAACCTAGAAAAA[C/G]ATTTCATTCCCCGGT | 7525 |
rs12956481 | snp | A/T | 0.456095 | 0.141508 | intron-variant | YES1 | GRCh38.p7 | 18:743916 | GACTCGAAAAAAAAA[A/T]AAATATATATATATA | 7525 |
rs12956482 | snp | A/T | 0.465052 | 0.127485 | intron-variant | YES1 | GRCh38.p7 | 18:743918 | CTCGAAAAAAAAAAA[A/T]ATATATATATATATA | 7525 |
rs12958089 | snp | C/T | 0.451732 | 0.147663 | intron-variant | YES1 | GRCh38.p7 | 18:755317 | GCAGTGGCGCAATCT[C/T]GGCTCACTGCAATCT | 7525 |
rs12959870 | snp | C/T | | | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:812351 | ccccggccccgcccc[C/T]TGACTTCTAGCGGGG | 7525 |
rs12960947 | snp | C/G | 0.0106949 | 0.0723399 | intron-variant | YES1 | GRCh38.p7 | 18:780433 | agagatcttagctta[C/G]cacaatagcacactc | 7525 |
rs12961275 | snp | A/G | 0.295854 | 0.245759 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723072 | ACTCCAGCCTGGGCG[A/G]CAGAGCGAGACTCCG | 7525 |
rs12962324 | snp | A/G | 0.077417 | 0.180873 | intron-variant | YES1 | GRCh38.p7 | 18:805472 | AACAACTTCAACTGC[A/G]GCAGAGCACACATTT | 7525 |
rs12962375 | snp | C/T | 0.480931 | 0.0957637 | intron-variant | YES1 | GRCh38.p7 | 18:768997 | atgagccactgtgcc[C/T]ggccctagatatgtt | 7525 |
rs12962742 | snp | A/T | 0.077417 | 0.180873 | intron-variant | YES1 | GRCh38.p7 | 18:807788 | AGAAGTTATCCCTCT[A/T]GAAGGCCTTCCACTT | 7525 |
rs12963050 | snp | C/T | 0.466308 | 0.125343 | intron-variant | YES1 | GRCh38.p7 | 18:807974 | TTGAACAAGAGAAAC[C/T]GAAGGGCATTGCTAC | 7525 |
rs12967001 | snp | A/G | 0.084728 | 0.187577 | intron-variant | YES1 | GRCh38.p7 | 18:737535 | TGGTTAGGAGAAGAG[A/G]TAAATCACAAGGTAA | 7525 |
rs12967818 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:787074 | AAAAACTGTGATACA[A/T]ACTGTCTTTTttttt | 7525 |
rs12967820 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:787081 | GTGATACATACTGTC[C/T]TTTtttttttttttt | 7525 |
rs12968093 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:741434 | tttgtagagatgggg[A/T]ttcaccatgttgctc | 7525 |
rs12968094 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:741436 | tgtagagatggggtt[C/T]caccatgttgctcag | 7525 |
rs12968123 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:741483 | GGCCCTCCCTTCCCC[C/T]CTGGTTCATCTAATA | 7525 |
rs12968865 | snp | A/G | 0.43978 | 0.162738 | intron-variant | YES1 | GRCh38.p7 | 18:772621 | ATTTTTAGTAGAGAC[A/G]GAGTTTCACCATGTT | 7525 |
rs12969606 | snp | A/C | 0.496583 | 0.0411924 | intron-variant | YES1 | GRCh38.p7 | 18:726161 | CCGGGTGCGGTGGCT[A/C]ATGCCTGTAATCCCA | 7525 |
rs12969944 | snp | A/G | 0.495671 | 0.0463237 | intron-variant | YES1 | GRCh38.p7 | 18:764796 | GGAGTGCAGTGGCGC[A/G]ATCTCGACTCACTGT | 7525 |
rs12970189 | snp | G/T | 0.0901694 | 0.192235 | intron-variant | YES1 | GRCh38.p7 | 18:789091 | CCTATACATGCTTTA[G/T]TTGCTTCTGATTGGA | 7525 |
rs12970623 | snp | A/G | 0.498734 | 0.0251279 | intron-variant | YES1 | GRCh38.p7 | 18:729159 | tctatgcattacctt[A/G]gatactttgttaatg | 7525 |
rs13313619 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | YES1 | GRCh38.p7 | 18:781472 | TCTTCCTTGATCTCC[C/T]ATGTGCTCACACAGT | 7525 |
rs13313625 | snp | A/G | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:779355 | gctgcggtaagttat[A/G]atcgcaccactgcac | 7525 |
rs13381986 | snp | A/C | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:760627 | tctagaaggctctac[A/C]atttcccatggatct | 7525 |
rs16949799 | snp | G/T | 0.0887219 | 0.191022 | intron-variant | YES1 | GRCh38.p7 | 18:746282 | ACTACTCAATGTGTC[G/T]CTCAAAACTCCACCT | 7525 |
rs16950778 | snp | A/G | 0.15665 | 0.231917 | intron-variant | YES1 | GRCh38.p7 | 18:807819 | CCTAGGAGAAAGTAG[A/G]GTCCAAAGAACCTAT | 7525 |
rs17516202 | snp | A/G | 0.234692 | 0.249531 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722644 | CTGAGTTACTCTTAA[A/G]AATTAGTCTTATTTT | 7525 |
rs17516216 | snp | A/G | 0.237593 | 0.249692 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722875 | AGGCGGGCAGATCAC[A/G]AGGTCAGGAGATCGA | 7525 |
rs17516223 | snp | A/G | 0.304438 | 0.244001 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723024 | GTGAACCTGGGAGGC[A/G]GAGCTTGCAGTGAGC | 7525 |
rs17516230 | snp | A/G | 0.252421 | 0.249988 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723036 | GGCRGAGCTTGCAGT[A/G]AGCCGASATCGYGCC | 7525 |
rs17516244 | in-del | -/A | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723104 | CTCAAAAAAGAAAAC[-/A]AAAAAAAGTGAATGT | 7525 |
rs17551206 | snp | C/T | 0.313082 | 0.241911 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722814 | GAAGTGAATGTAGGC[C/T]GGGCGCGGTGGCTCA | 7525 |
rs17551213 | snp | A/G | 0.239326 | 0.249772 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722819 | GAATGTAGGCTGGGC[A/G]CGGTGGCTCACGCCT | 7525 |
rs17551227 | snp | A/G | 0.00318978 | 0.0398085 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722831 | GGCRCGGTGGCTCAY[A/G]CCTGTAATCCCAGCA | 7525 |
rs17551234 | snp | C/G | 0.278399 | 0.248382 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723043 | CTTGCAGTRAGCCGA[C/G]ATCGYGCCACTGCAC | 7525 |
rs17551241 | snp | C/T | 0.284995 | 0.247539 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723048 | AGTGAGCCGAGATCG[C/T]GCCACTGCACTCCAG | 7525 |
rs17551248 | snp | A/G | 0.249603 | 0.25 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723069 | TGCACTCCAGCCTGG[A/G]YGRCAGAGCGAGACT | 7525 |
rs17551255 | snp | C/T | 0.24932 | 0.249999 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723070 | GCACTCCAGCCTGGG[C/T]GACAGAGCGAGACTC | 7525 |
rs28375888 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:787057 | CAAAATTATGTTTTT[A/T]AAAAAACTGTGATAC | 7525 |
rs28379083 | snp | A/G | 0.0592355 | 0.161582 | intron-variant | YES1 | GRCh38.p7 | 18:798546 | ATGGTGAGAAGATGC[A/G]TAGGGGAGCCGCTTT | 7525 |
rs28397183 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | YES1 | GRCh38.p7 | 18:755646 | CTTTTGCACCCACTG[A/G]CTGTTAATGAGGACA | 7525 |
rs28428835 | snp | A/G | 0.0558544 | 0.157504 | intron-variant | YES1 | GRCh38.p7 | 18:755300 | GTCACCTAGGCTGGA[A/G]TGCAGTGGCGCAATC | 7525 |
rs28525517 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:735668 | GCAGTGAGCCGAGAT[C/T]GTGCCGCTACACTCC | 7525 |
rs28560341 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:748719 | ATAGCATGTCTATCA[C/G]TAGTTCATTCTTTAC | 7525 |
rs28621567 | snp | C/T | | | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:775965 | CATAGGTAAGGGATA[C/T]GAATTGTTTCCAGTT | 7525 |
rs28716335 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | YES1 | GRCh38.p7 | 18:735676 | CCGAGATCGTGCCGC[C/T]ACACTCCAGCCTGGG | 7525 |
rs28722141 | snp | A/G | 0.244205 | 0.249933 | intron-variant | YES1 | GRCh38.p7 | 18:737036 | ACAATTATGGTTAAT[A/G]TCAAATTGTGTCACT | 7525 |
rs28806909 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:769154 | GCTGTACCATCTAGG[C/T]TTATGTAAGCACACT | 7525 |
rs34097423 | in-del | -/T | | | intron-variant | YES1 | GRCh38.p7 | 18:758082 | ATAATTTTAAATTTT[-/T]CTAATTTAGTGTAGC | 7525 |
rs34146975 | in-del | -/G | | | intron-variant | YES1 | GRCh38.p7 | 18:750824 | AAAGGAAAGAAATGG[-/G]AAAGATGAGAAATCA | 7525 |
rs34175587 | in-del | -/C | | | intron-variant | YES1 | GRCh38.p7 | 18:789809 | CAAGCCTGTAATCCC[-/C]AGCACTTTGGGAGGC | 7525 |
rs34197266 | in-del | -/T | | | intron-variant | YES1 | GRCh38.p7 | 18:789089 | ACCTATACATGCTTT[-/T]AGTTGCTTCTGATTG | 7525 |
rs34197309 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:744407 | TTCTTTTTTTTTTTT[G/T]GAGATGGAGTCTCAC | 7525 |
rs34204766 | in-del | -/G | | | intron-variant | YES1 | GRCh38.p7 | 18:756149 | TCGCTACTCTACTGT[-/G]CATTTAATTAACATC | 7525 |
rs34207897 | in-del | -/TCT | | | intron-variant | YES1 | GRCh38.p7 | 18:727596 | GGCTTTTTGTCTTCT[-/TCT]CTTGTTATTTTAGTA | 7525 |
rs34293878 | in-del | -/T | | | intron-variant | YES1 | GRCh38.p7 | 18:747777 | TAGTTATTAATTTTT[-/T]AAGTAACATCTATTA | 7525 |
rs34302612 | in-del | -/T | 0.5 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:773839 | TAAAACACTTTTCCC[-/T]TTTTTTTTTTGAGAC | 7525 |
rs34311794 | in-del | -/G | | | intron-variant | YES1 | GRCh38.p7 | 18:725926 | TTTTACTAACAGTGG[-/G]AAATACAACTAGAAG | 7525 |
rs34345157 | in-del | -/A | | | intron-variant | YES1 | GRCh38.p7 | 18:807528 | CACAAAAACACAAAA[-/A]GATGCGACTGCTGCT | 7525 |
rs34365852 | in-del | -/C | | | intron-variant | YES1 | GRCh38.p7 | 18:753164 | CAGGTTAAAAACTCC[-/C]ATAATATATTAATAT | 7525 |
rs34368519 | in-del | -/A | | | intron-variant | YES1 | GRCh38.p7 | 18:738042 | GCTCACAAAACCTAA[-/A]TTTTTTTTTTTTTTT | 7525 |
rs34413141 | snp | A/T | 0.379746 | 0.213696 | intron-variant | YES1 | GRCh38.p7 | 18:777281 | TTTTATATATGTATA[A/T]AAAGACATTCATTTA | 7525 |
rs34440107 | in-del | -/A | | | intron-variant | YES1 | GRCh38.p7 | 18:751881 | GCCAAAAAAAAAAAA[-/A]GCTTAAGGATAGTTT | 7525 |
rs34461070 | in-del | -/A | | | intron-variant | YES1 | GRCh38.p7 | 18:787722 | TCAAAAAAAAAAAAA[-/A]TATTCTGTTGAATTA | 7525 |
rs34478842 | in-del | -/T | | | intron-variant | YES1 | GRCh38.p7 | 18:803552 | CTGTCCTATAGGGTT[-/T]AGAGTATGAGGCAGG | 7525 |
rs34520535 | in-del | -/G | | | intron-variant | YES1 | GRCh38.p7 | 18:747103 | ATATTCTTTCATGGG[-/G]CATATTACTTTTATA | 7525 |
rs34580680 | snp | C/T | 0.00871863 | 0.0654469 | missense | YES1 | GRCh38.p7 | 18:745840 | CATCCCAATCACGAA[C/T]AGAAAGGGAATAAGC | 7525 |
rs34621909 | in-del | -/G | | | intron-variant | YES1 | GRCh38.p7 | 18:763611 | GGAGGTTGAGGTGGG[-/G]AAGATCACCTGAGCC | 7525 |
rs34663012 | in-del | -/A | | | intron-variant | YES1 | GRCh38.p7 | 18:772363 | CAGGTCTTGATACTA[-/A]GGTAAACATTGCTTT | 7525 |
rs34717750 | in-del | -/A | | | intron-variant | YES1 | GRCh38.p7 | 18:807332 | AGTGATACTTCATCA[-/A]AAAAAAAAAAAAAAA | 7525 |
rs34720616 | in-del | -/C | | | intron-variant | YES1 | GRCh38.p7 | 18:780945 | CCCCCTCTTTCTCCC[-/C]AATATAAAGTCCAAA | 7525 |
rs34736830 | in-del | -/A | | | intron-variant | YES1 | GRCh38.p7 | 18:778929 | GTTAGCAATGGACAA[-/A]CTGATCTTGCAGGGG | 7525 |
rs34753979 | in-del | -/G | 0.308166 | 0.243139 | intron-variant | YES1 | GRCh38.p7 | 18:736335 | GGGGGGAAGGGGGGG[-/G]TTTGCCTGCACATTT | 7525 |
rs34756879 | in-del | -/T | | | intron-variant | YES1 | GRCh38.p7 | 18:773820 | GTTCTCTCTCTCTCT[-/T]CCTTAAAACACTTTT | 7525 |
rs34760851 | in-del | -/T | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:783051 | TAACTTTTTTTTTTT[-/T]AAGAAAAGTATGTAA | 7525 |
rs34769090 | in-del | -/AC | 0.481917 | 0.0933517 | intron-variant | YES1 | GRCh38.p7 | 18:783391 | GGTTATGTAGGGGAA[-/AC]ACACACACACACACA | 7525 |
rs34784111 | in-del | -/G | | | intron-variant | YES1 | GRCh38.p7 | 18:796387 | AGTATTTATACAGGG[-/G]ACTGTCACACAGTCA | 7525 |
rs34834803 | in-del | -/C | | | downstream-variant-500B | YES1 | GRCh38.p7 | 18:721287 | CACGCCTGTAATCCC[-/C]AGCACTTTGGGAGGC | 7525 |
rs34840844 | in-del | -/C | | | intron-variant | YES1 | GRCh38.p7 | 18:791228 | CACTCCAGCCTGGCC[-/C]AACAAGAGTGAAACT | 7525 |
rs34878895 | in-del | -/AC/ACAC/CA | 0.0786417 | 0.184972 | intron-variant | YES1 | GRCh38.p7 | 18:783392 | TTATGTAGGGGAAAC[-/AC/ACAC/CA]ACACACACACACACA | 7525 |
rs34970099 | in-del | -/A/AAA | 0.499824 | 0.00938333 | intron-variant | YES1 | GRCh38.p7 | 18:728322 | TCAAAAAAAAAAAAA[-/A/AAA]TTCATTTATGTTTCA | 7525 |
rs35003724 | in-del | -/A | | | intron-variant | YES1 | GRCh38.p7 | 18:779419 | AAAAAAAAAAAAAAA[-/A]GAAAGAAAGAAATGT | 7525 |
rs35073440 | in-del | -/A | | | intron-variant | YES1 | GRCh38.p7 | 18:777826 | AAAAAAAAAAAAAAA[-/A]TTAAAAAAAGAATTA | 7525 |
rs35078982 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:808560 | TGAACTGAAGGTGAC[C/T]TAAGCCATGTAGGGT | 7525 |
rs35119453 | in-del | -/TG | | | intron-variant | YES1 | GRCh38.p7 | 18:735576 | AAAATTAGCTGGGTG[-/TG]GTGGTACGAGCCTGT | 7525 |
rs35126906 | snp | C/T | 1.64787e-05 | 0.00287038 | missense | YES1 | GRCh38.p7 | 18:743295 | CATCCTTGTCCTAGT[C/T]TAACCTCTAGTCGCA | 7525 |
rs35186688 | in-del | -/A | | | intron-variant | YES1 | GRCh38.p7 | 18:735737 | AAACAAACAAAAAAA[-/A]CCTACATATTGGGTA | 7525 |
rs35188047 | in-del | -/AA | 0.499053 | 0.0217445 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722010 | AAATGAATACACATT[-/AA]GTTAGTGTTTTATCC | 7525 |
rs35200359 | in-del | -/G | | | intron-variant | YES1 | GRCh38.p7 | 18:782887 | TTAGTAGAGACAGGG[-/G]TTTCGCCATATTAGC | 7525 |
rs35217977 | in-del | -/A | | | intron-variant | YES1 | GRCh38.p7 | 18:785779 | ACAAAAGGAAAAAAA[-/A]AAAAAAAGCCAGGCG | 7525 |
rs35222892 | in-del | -/C | | | intron-variant | YES1 | GRCh38.p7 | 18:724694 | CTAGGAAAACATAAC[-/C]AAACCCCCTAGCCAC | 7525 |
rs35270236 | in-del | -/T | | | intron-variant | YES1 | GRCh38.p7 | 18:779712 | TCAAGAATCTTTATT[-/T]CTCTCAGATTTTCAC | 7525 |
rs35276880 | in-del | -/G | | | intron-variant | YES1 | GRCh38.p7 | 18:736080 | GGAGGCTGAGGTGGG[-/G]AGGATCACCTGAGCC | 7525 |
rs35424900 | in-del | -/TC | | | intron-variant | YES1 | GRCh38.p7 | 18:758624 | ACAAATGTTACTTTT[-/TC]CCATTCAGGCTTTCC | 7525 |
rs35443320 | in-del | -/G | | | intron-variant | YES1 | GRCh38.p7 | 18:735485 | TAATGGACTTTGGGG[-/G]AGTAAGGGGGAAAGG | 7525 |
rs35481075 | in-del | -/A | 0.494526 | 0.0520291 | intron-variant | YES1 | GRCh38.p7 | 18:748798 | TTACTCATTTTAGAT[-/A]AAAAAAAAAATCACA | 7525 |
rs35530008 | in-del | -/A | 0.418491 | 0.184691 | intron-variant | YES1 | GRCh38.p7 | 18:754713 | AGAGACTCCAACTCC[-/A]AAAAAAAAAAAAAAA | 7525 |
rs35650990 | in-del | -/G | | | intron-variant | YES1 | GRCh38.p7 | 18:763631 | CACCTGAGCCCAGGG[-/G]AGGTCAAGGCTGCAG | 7525 |
rs35701098 | in-del | -/G | | | intron-variant | YES1 | GRCh38.p7 | 18:797091 | TATGCACAGACATGG[-/G]AAAAGTCTTTGCAAC | 7525 |
rs35743931 | in-del | -/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:776199 | TCTTTTTTTTTTTTT[-/T]GAGATGGAGTCTCCC | 7525 |
rs35784531 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:726431 | CTCCATCTCAAAAAC[A/C]CAAAAACAAAAACAA | 7525 |
rs35789125 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:738139 | GTGGCATATGCCTGT[G/T]GCCTATGTATAGTTT | 7525 |
rs35791131 | in-del | -/G | | | intron-variant | YES1 | GRCh38.p7 | 18:755294 | CGCTCTGTCACCTAG[-/G]CTGGAATGCAGTGGC | 7525 |
rs35903752 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:755982 | GCTATTCTCTAAAAG[C/G]ATATAATAATGTAAT | 7525 |
rs35944475 | in-del | -/A | | | intron-variant | YES1 | GRCh38.p7 | 18:753131 | ATCTCAGTGTTAAAA[-/A]TTATTCAAGGCAGGT | 7525 |
rs36004586 | in-del | -/A | 0.0626037 | 0.165477 | intron-variant | YES1 | GRCh38.p7 | 18:769040 | CTTACCATTGTGTTA[-/A]CAACTGCCTACAGCA | 7525 |
rs36125135 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:736268 | AAGAAAGCACTATGT[C/T]TAAAGCAGGGTTTCT | 7525 |
rs55771020 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723565 | CTAGTTTTTAAAAAG[A/G]GCTTTTAAAATGCTG | 7525 |
rs55771515 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:730960 | AGAGAAGGGTGAAAT[A/C]AGCAAAGGAGTGATT | 7525 |
rs55786323 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:752797 | AAAATACAAAAATTA[A/G]CCAGGCATGGTGGCG | 7525 |
rs55834938 | in-del | -/CC | | | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:812338 | CTCCGCCCCCCCCCC[-/CC]GGCCCCGCCCCCTGA | 7525 |
rs55836893 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:783824 | TCACCATGTTGGCCA[G/T]GCTAGTCTTGAACGC | 7525 |
rs55997550 | snp | C/T | 0.359364 | 0.22481 | intron-variant | YES1 | GRCh38.p7 | 18:783619 | TATCAATTTTTCTCT[C/T]TTTTTTTTTTTTTTG | 7525 |
rs56044917 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:771760 | TTGTCATGTTGCCCA[G/T]GCTGGGCACAGGGAT | 7525 |
rs56069306 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:752294 | TTTGTATTTTTAGTA[C/G]AGACAGGGTTTCACT | 7525 |
rs56103667 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:752707 | CAGCACTTTGGGAGG[C/T]CGAGGTGGGCAAATC | 7525 |
rs56158078 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:752741 | TGAGGCCAGGAGTTC[A/G]AGACCAGCCTGGTCA | 7525 |
rs56171861 | snp | C/T | 0.5 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:755682 | TGCTTGATTTGATGC[C/T]GGCAGCTGTTTTGCC | 7525 |
rs56260033 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | YES1 | GRCh38.p7 | 18:751064 | AGTAGAAGGATATGA[A/C]CATATTTTATGTTCC | 7525 |
rs56262734 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:752748 | AGGAGTTCGAGACCA[A/G]CCTGGTCAACAGGGC | 7525 |
rs56301539 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:752776 | GGCGAAACCCTGTCT[C/G]TACTAAAAATACAAA | 7525 |
rs56303611 | snp | C/T | 0.241627 | 0.24986 | intron-variant | YES1 | GRCh38.p7 | 18:752041 | TAGTCTTAAACTCTC[C/T]GAAGACCTTCCATAA | 7525 |
rs56329509 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:752812 | GCCAGGCATGGTGGC[A/G]CATGCCTGTAATCTC | 7525 |
rs56342716 | in-del | -/AT | 0.449218 | 0.151037 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723394 | TTGTAAAACTTTCAC[-/AT]TTTCTTTTCTCGTAT | 7525 |
rs56385527 | in-del | -/AA | | | intron-variant | YES1 | GRCh38.p7 | 18:752793 | CTAAAAATACAAAAA[-/AA]TTAGCCAGGCATGGT | 7525 |
rs56410052 | in-del | -/CACA/CACACACA | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:786537 | ACACACACACACACA[-/CACA/CACACACA]GAGTTGCTCCTCATT | 7525 |
rs56748581 | in-del | -/AAAAAAAAA/AAAAAAAAAAA | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:804925 | CTCAAAAAAAAAAAA[-/AAAAAAAAA/AAAAAAAAAAA]CACAAACCAAAAACC | 7525 |
rs56793935 | snp | C/G | 0.084364 | 0.187256 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722918 | TAACACGGTGAAACT[C/G]CGTCTCTACTAAAAA | 7525 |
rs57239746 | snp | C/T | 0.0372196 | 0.131242 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722280 | CCTCTTGGTAGAGAG[C/T]GTCAATACTAAGCAG | 7525 |
rs57321321 | snp | C/G | 0.15665 | 0.231917 | intron-variant | YES1 | GRCh38.p7 | 18:785546 | TGGCATTACATCCAG[C/G]CTGTTCAGATGATAC | 7525 |
rs57896154 | in-del | -/A | | | intron-variant | YES1 | GRCh38.p7 | 18:804630 | AAAAAAAAAAAAAAA[-/A]GGCCAGCTGAGGTGG | 7525 |
rs57905842 | snp | C/G/T | 0.000153988 | 0.00877328 | synonymous-codon, missense | YES1 | GRCh38.p7 | 18:739735 | TATATATACAGATAC[C/G/T]TGAGCAGCCATATCA | 7525 |
rs58064430 | in-del | -/A | | | intron-variant | YES1 | GRCh38.p7 | 18:804630 | AAAAAAAAAAAAAAA[-/A]GGCCAGCTGAGGTGG | 7525 |
rs58178670 | snp | A/C | 0.029116 | 0.117091 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722914 | TGGCTAACACGGTGA[A/C]ACTGCGTCTCTACTA | 7525 |
rs58213671 | snp | C/T | 0.200182 | 0.244986 | intron-variant | YES1 | GRCh38.p7 | 18:743797 | TGTAGTCTCAGCTAC[C/T]AAGGAAGCTGAGGCA | 7525 |
rs58238073 | snp | A/T | 0.460477 | 0.134905 | intron-variant | YES1 | GRCh38.p7 | 18:766847 | CTAACACTATTATAT[A/T]CTTTATATATTCTGG | 7525 |
rs58322434 | in-del | -/AA | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:726814 | AAAAAAAAAAAAAAA[-/AA]TTCACATGGTAAATA | 7525 |
rs58595025 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | YES1 | GRCh38.p7 | 18:735385 | TTATTCTAAGTGAAG[C/T]AACTCAGGGATGGAA | 7525 |
rs58789989 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | YES1 | GRCh38.p7 | 18:754565 | CAAAAAAAATTAGCC[A/G]GGTGCCGTGGTGTTT | 7525 |
rs58895273 | snp | A/C | 0.0770498 | 0.180522 | intron-variant | YES1 | GRCh38.p7 | 18:760656 | CTTGAGGGATGACTA[A/C]AGTGAAAATATTGTA | 7525 |
rs58976039 | snp | C/T | 0.154661 | 0.231107 | intron-variant | YES1 | GRCh38.p7 | 18:810979 | ATTAGATTTACCATG[C/T]ACTTTTCCTTAAATG | 7525 |
rs58982033 | snp | A/G | 0.157642 | 0.232314 | intron-variant | YES1 | GRCh38.p7 | 18:796121 | CACAATGAAGTTCAC[A/G]TGAAAAAGTAAATGC | 7525 |
rs59022424 | in-del | -/AAT | | | intron-variant | YES1 | GRCh38.p7 | 18:728001 | TATTTGCATATACAT[-/AAT]GAGATATCTTAAGGG | 7525 |
rs59032922 | snp | A/G | 0.243633 | 0.249919 | intron-variant | YES1 | GRCh38.p7 | 18:735283 | AGTGGATAAAAAAAA[A/G]TGTGGCATATATACA | 7525 |
rs59184545 | snp | A/T | 0.185155 | 0.241444 | intron-variant | YES1 | GRCh38.p7 | 18:786369 | CTTCACATAAGAGTG[A/T]CAAGTTTGAGGGACA | 7525 |
rs59360060 | in-del | -/CT/GGGCAAGGTAACT/GGTAACT | | | intron-variant | YES1 | GRCh38.p7 | 18:730961 | AGAAGGGTGAAATCA[-/CT/GGGCAAGGTAACT/GGTAACT]GCAAAGGAGTGATTA | 7525 |
rs59582095 | in-del | -/AAAA | 0.472896 | 0.113214 | intron-variant | YES1 | GRCh38.p7 | 18:742460 | CCCCAGTCTCTATTT[-/AAAA]AAAAAAAAAAAAAGA | 7525 |
rs59710020 | snp | C/T | 0.0041672 | 0.0454559 | intron-variant | YES1 | GRCh38.p7 | 18:751837 | GACCAAGGTAAATTA[C/T]GTAGCTAACTTAACA | 7525 |
rs59787531 | in-del | -/TTTTT | | | intron-variant | YES1 | GRCh38.p7 | 18:730358 | ATTTTTTTTTTTTTT[-/TTTTT]GAGACAGGGTCTTGC | 7525 |
rs59892406 | snp | C/T | 0.156319 | 0.231784 | intron-variant | YES1 | GRCh38.p7 | 18:810477 | ATGAACAGAAAGGAA[C/T]CAATTTTGTGGTTTA | 7525 |
rs60315447 | snp | A/G | 0.089084 | 0.191327 | intron-variant | YES1 | GRCh38.p7 | 18:749733 | GACGTGGTGGCGGGC[A/G]CCTGTAGTCCCAGCT | 7525 |
rs60377646 | snp | C/T | 0.199873 | 0.244923 | intron-variant | YES1 | GRCh38.p7 | 18:740726 | AGGACTTTTGTTATC[C/T]TGTATTCTAAATCTC | 7525 |
rs60542745 | in-del | -/AGATA | | | intron-variant | YES1 | GRCh38.p7 | 18:810960 | GCACTGTGATAGTTA[-/AGATA]TTAGATTTACCATGC | 7525 |
rs60612957 | snp | A/G | 0.0232847 | 0.105357 | downstream-variant-500B | YES1 | GRCh38.p7 | 18:721407 | GCCGGGCGTGGTAGC[A/G]GGCGCCTGTAGTCCC | 7525 |
rs60798182 | in-del | -/GG | 0.46885 | 0.12085 | intron-variant | YES1 | GRCh38.p7 | 18:730958 | CAGAGAAGGGTGAAA[-/GG]TCAGCAAAGGAGTGA | 7525 |
rs61052658 | snp | A/G | 0.132751 | 0.2208 | intron-variant | YES1 | GRCh38.p7 | 18:757270 | GCACTTTGGGAGGCC[A/G]AGGCGGGCGGATCAC | 7525 |
rs61125455 | in-del | -/AAT | | | intron-variant | YES1 | GRCh38.p7 | 18:726814 | AAAAAAAAAAAAAAA[-/AAT]TCACATGGTAAATAC | 7525 |
rs61216473 | in-del | -/GGGCAAGGT | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:730957 | TCAGAGAAGGGTGAA[-/GGGCAAGGT]ATCAGCAAAGGAGTG | 7525 |
rs61439561 | in-del | -/TACTTTG | 0.00358779 | 0.0422022 | intron-variant | YES1 | GRCh38.p7 | 18:804360 | CGCCTGTAATCCCAA[-/TACTTTG]GGAGGCCAAGGCAGG | 7525 |
rs61607425 | in-del | -/CACACACACACA/CACACACACACACACA | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:795945 | ACACACACACACACA[lengthTooLong]TAAGACCTATGAGTA | 7525 |
rs61734346 | snp | C/T | 0.000922053 | 0.0214517 | missense | YES1 | GRCh38.p7 | 18:756716 | GACATGGTGACACTG[C/T]AGTGGGTTCTGCTCC | 7525 |
rs62088288 | snp | C/T | 0.199873 | 0.244923 | intron-variant | YES1 | GRCh38.p7 | 18:734171 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 7525 |
rs62088289 | snp | C/T | 0.243633 | 0.249919 | intron-variant | YES1 | GRCh38.p7 | 18:734427 | AGCCGAGCTTGGTGG[C/T]AGGCACCTGTAGTCC | 7525 |
rs62088290 | snp | A/G | 0.243919 | 0.249926 | intron-variant | YES1 | GRCh38.p7 | 18:734809 | AACTCCTTAAAGAAC[A/G]AAAAGCAGAACTACC | 7525 |
rs62088291 | snp | G/T | 0.224412 | 0.248687 | intron-variant | YES1 | GRCh38.p7 | 18:734985 | CAACATGGTGAAACC[G/T]TGTCTCTACTAAAAT | 7525 |
rs62088292 | snp | A/G | 0.243633 | 0.249919 | intron-variant | YES1 | GRCh38.p7 | 18:735026 | GCCGGGCCTGGTGGC[A/G]GGTGCCTGTAATCCC | 7525 |
rs62088293 | snp | A/T | 0.199564 | 0.24486 | intron-variant | YES1 | GRCh38.p7 | 18:739085 | CCACCTCGGCCTCTC[A/T]AAGTGCTCAGATTAC | 7525 |
rs62088294 | snp | C/T | 0.199564 | 0.24486 | intron-variant | YES1 | GRCh38.p7 | 18:742161 | ACATAAAAATCAGGC[C/T]TGTCAGCTTATCTGC | 7525 |
rs62088295 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:743526 | AAACAGAAGTCCTTT[C/T]GAGTTTTACTCTAAA | 7525 |
rs62088296 | snp | A/G | 0.199873 | 0.244923 | intron-variant | YES1 | GRCh38.p7 | 18:749721 | AAAAATTAGCCAGAC[A/G]TGGTGGCGGGCGCCT | 7525 |
rs62088297 | snp | C/T | 0.192401 | 0.243274 | intron-variant | YES1 | GRCh38.p7 | 18:750538 | AACCAAAAATGTCTC[C/T]AGATACTGCCAAATA | 7525 |
rs62088299 | snp | A/C | 0.199564 | 0.24486 | intron-variant | YES1 | GRCh38.p7 | 18:754784 | TGATTAACTGCAGGG[A/C]CTTCACCATCATTCT | 7525 |
rs62088300 | snp | C/T | 0.20111 | 0.245173 | intron-variant | YES1 | GRCh38.p7 | 18:755637 | GGGATTTATCTTTTG[C/T]ACCCACTGGCTGTTA | 7525 |
rs62088301 | snp | C/T | 0.206947 | 0.246265 | intron-variant | YES1 | GRCh38.p7 | 18:758137 | AGGTAAAATTAACTT[C/T]AGTATTTTATTTAAC | 7525 |
rs62088302 | snp | C/T | 0.236724 | 0.249647 | intron-variant | YES1 | GRCh38.p7 | 18:758348 | GACAAAGTAGATCTA[C/T]ACCTTTTCCCTTCCC | 7525 |
rs62088303 | snp | A/G | 0.209388 | 0.246679 | intron-variant | YES1 | GRCh38.p7 | 18:759650 | AAACAACATAGTACA[A/G]TAACTATTTACACTG | 7525 |
rs62088304 | snp | C/G | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:764115 | ACAGAGCGAGACTCC[C/G]TCTCAAAAAAAAAAA | 7525 |
rs62088305 | snp | A/G | 0.467744 | 0.122832 | intron-variant | YES1 | GRCh38.p7 | 18:764284 | CTAGAGCACAATGGT[A/G]CAATCCCGGCACACT | 7525 |
rs62088306 | snp | C/T | 0.466308 | 0.125343 | intron-variant | YES1 | GRCh38.p7 | 18:765056 | ATCTTTTAAAGATAA[C/T]AGAACTCTCAAATAA | 7525 |
rs62088307 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | YES1 | GRCh38.p7 | 18:765103 | AAATCAAAAGAATTA[A/T]CACAATGTTGGAGGA | 7525 |
rs62088308 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | YES1 | GRCh38.p7 | 18:771310 | AGGCGGAGGTTGCAG[G/T]GAGCCAAGATTGCAC | 7525 |
rs62088309 | snp | C/T | 0.5 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:779907 | AACAATGTATGTAGT[C/T]CTTTTTTTTTTTTTT | 7525 |
rs62088310 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:781776 | TTCCTTTTTTTTTTG[G/T]AGGAATAATACCTAT | 7525 |
rs62088356 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:795868 | TGGCACATGTGTACC[C/T]ATGTAACAAACCTGC | 7525 |
rs62088357 | snp | C/G | 0.208779 | 0.246578 | intron-variant | YES1 | GRCh38.p7 | 18:798400 | TAAGAGCTTCACAAC[C/G]CTCTTTTCTACTTGA | 7525 |
rs62088358 | snp | A/G | 0.103438 | 0.202533 | intron-variant | YES1 | GRCh38.p7 | 18:811723 | ACCCCCAGCCTTTAG[A/G]ACCCAAAGGGGCCGC | 7525 |
rs62088359 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:814129 | GCTTCTCTTCGCCCT[C/T]CCTTTTTTTTTTTAT | 7525 |
rs62091703 | snp | C/T | 0.253824 | 0.249971 | intron-variant | YES1 | GRCh38.p7 | 18:725062 | TTTTGCCAAATATAC[C/T]AACTACATAACTTTA | 7525 |
rs62091704 | snp | A/G | 0.253824 | 0.249971 | intron-variant | YES1 | GRCh38.p7 | 18:725844 | AGCCGAGATTGCGCC[A/G]TAGCACTCCAGCCTG | 7525 |
rs62091705 | snp | C/T | 0.254105 | 0.249966 | intron-variant | YES1 | GRCh38.p7 | 18:727228 | TTTATTATTATGAAA[C/T]GTCCCTTTTTGTCCC | 7525 |
rs62091706 | snp | G/T | 0.252421 | 0.249988 | intron-variant | YES1 | GRCh38.p7 | 18:728485 | AATTTTCCATTTGTG[G/T]TGTTATGTCAATGCT | 7525 |
rs62091707 | snp | C/T | 0.237303 | 0.249677 | intron-variant | YES1 | GRCh38.p7 | 18:730454 | GGCTCAAGCGATCCA[C/T]CCACCTTAGCCTCCC | 7525 |
rs62091708 | snp | C/T | 0.208474 | 0.246527 | intron-variant | YES1 | GRCh38.p7 | 18:731318 | TGTGTATTAAGATGA[C/T]AATGAGTTAAGACAG | 7525 |
rs62091709 | snp | C/T | 0.214541 | 0.247473 | intron-variant | YES1 | GRCh38.p7 | 18:731545 | CTAAAGATTAAATTT[C/T]ATATGCTTTCACTCT | 7525 |
rs62091710 | snp | C/T | 0.201418 | 0.245234 | intron-variant | YES1 | GRCh38.p7 | 18:731923 | AGTGAGCTGAGATCG[C/T]GCCACTGCACTCCAG | 7525 |
rs62091711 | snp | A/G | 0.20111 | 0.245173 | intron-variant | YES1 | GRCh38.p7 | 18:731924 | GTGAGCTGAGATCGT[A/G]CCACTGCACTCCAGC | 7525 |
rs62091712 | snp | C/T | 0.242488 | 0.249887 | intron-variant | YES1 | GRCh38.p7 | 18:733399 | AAAATTTTATTGTAC[C/T]ACTTTTAAAAGTCCA | 7525 |
rs66563455 | snp | C/T | 0.378962 | 0.21417 | intron-variant | YES1 | GRCh38.p7 | 18:786568 | ATTTTGAATTCCATA[C/T]TTATGAATTCACCTG | 7525 |
rs67285587 | snp | A/C | 0.478104 | 0.102316 | intron-variant | YES1 | GRCh38.p7 | 18:780355 | TCCATGTATGGATTA[A/C]TAAAGGATAAATGGA | 7525 |
rs67819665 | in-del | -/T | | | intron-variant | YES1 | GRCh38.p7 | 18:726816 | AAAAAAAAAAAAAAA[-/T]TCACATGGTAAATAC | 7525 |
rs68020784 | in-del | -/T | 0.350109 | 0.229081 | intron-variant | YES1 | GRCh38.p7 | 18:783040 | ACTACAAAGGTTAAC[-/T]TTTTTTTTTTTAAGA | 7525 |
rs71174278 | in-del | -/CTT | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:727599 | TTTTTGTCTTCTCTT[-/CTT]GTTATTTTAGTAGTT | 7525 |
rs71174280 | in-del | -/AAAAAA | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:733805 | AAAAAAAAAAAAAAA[-/AAAAAA]GCATGGCTTTCATGA | 7525 |
rs71174281 | in-del | -/AAAAAAA | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:735174 | GCAAAAAAAAAAAAA[-/AAAAAAA]TCATTATATGAAAAA | 7525 |
rs71174282 | in-del | -/A | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:738712 | AAAAAAAAAAAAAAA[-/A]TTCAGCATACACTTT | 7525 |
rs71174284 | in-del | -/T | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:744715 | TTTTTTTTTTTTTTT[-/T]AAGAGATGAGGTCTT | 7525 |
rs71174285 | in-del | -/TT | 0.465996 | 0.12588 | intron-variant | YES1 | GRCh38.p7 | 18:759703 | ACAATTTATTTATTT[-/TT]CTTTTTTTCTTTTAT | 7525 |
rs71174286 | in-del | -/A | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:763704 | AAAAAAAAAAAAAAA[-/A]GACGAGCTGGAACAG | 7525 |
rs71174288 | in-del | -/ATAT | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:765290 | TATATATATATATAT[-/ATAT]CTGTAGCAATTTTTT | 7525 |
rs71174289 | in-del | -/TGAACTCTTCTGTAAGTC | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:767082 | ACTCTTCTGTAAGTC[-/TGAACTCTTCTGTAAGTC]AGGCCTATCAAGCCA | 7525 |
rs71174290 | in-del | -/T | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:787114 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTCAC | 7525 |
rs71174291 | in-del | -/CC | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:792557 | CTCTCTCTCTCTCCC[-/CC]TCTGTATATGTGTGT | 7525 |
rs71174292 | in-del | -/GTGTGTGT | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:792579 | TATGTGTGTGTGTGT[-/GTGTGTGT]ATATACATATATACA | 7525 |
rs71174293 | in-del | -/TT | 0.170408 | 0.236992 | intron-variant | YES1 | GRCh38.p7 | 18:810010 | GAATTTCCTTGCAGG[-/TT]TTTTTTTTTTTTTAA | 7525 |
rs71352966 | snp | A/T | 0.5 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:732468 | AAAAAAAAAACACCA[A/T]TCACACTGCTGGGAA | 7525 |
rs71352967 | snp | C/T | 0.0850919 | 0.187897 | intron-variant | YES1 | GRCh38.p7 | 18:735289 | TAAAAAAAAATGTGG[C/T]ATATATACACCATGG | 7525 |
rs71352968 | snp | C/T | 0.5 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:786808 | ATATACCTGCATGTT[C/T]TGAAGGACTTCATTC | 7525 |
rs71358757 | snp | A/G | 0.089084 | 0.191327 | intron-variant | YES1 | GRCh38.p7 | 18:787128 | TTGAGACAGAGTCTC[A/G]CTCTGTGGCCCAGGC | 7525 |
rs71363261 | in-del | -/T/TT | 0.197082 | 0.244335 | intron-variant | YES1 | GRCh38.p7 | 18:748360 | CTCAGTATTCTTTTC[-/T/TT]CTTTTTTTTTTTTTT | 7525 |
rs71363262 | in-del | -/TCTGTAAGTCTGAACTCT | 0.425123 | 0.178415 | intron-variant | YES1 | GRCh38.p7 | 18:767054 | TTTTCTACATGTTCA[-/TCTGTAAGTCTGAACTCT]TCTGTAAGTCTGAAC | 7525 |
rs71363264 | in-del | -/CTTAC | 0.093777 | 0.195178 | intron-variant | YES1 | GRCh38.p7 | 18:769422 | ACGTCTTTTTCCCTG[-/CTTAC]CTTATTCACTGACTA | 7525 |
rs71363266 | in-del | -/AAATAA | 0.5 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:781289 | AAAAAAAAAAAAAAA[-/AAATAA]GAGGGCCTTGTATGA | 7525 |
rs71805434 | in-del | -/T | 0.465996 | 0.12588 | intron-variant | YES1 | GRCh38.p7 | 18:783618 | GTATCAATTTTTCTC[-/T]TTTTTTTTTTTTTTT | 7525 |
rs71977266 | in-del | -/TATATATATATATATATATATATATATA | | | intron-variant | YES1 | GRCh38.p7 | 18:765249 | GGAAAGAGTTACAAC[-/TATATATATATATATATATATATATATA]TATATATATATATAT | 7525 |
rs72166719 | in-del | -/TAAGA | 0.157642 | 0.232314 | intron-variant | YES1 | GRCh38.p7 | 18:810958 | AAGCACTGTGATAGT[-/TAAGA]TATTAGATTTACCAT | 7525 |
rs72194254 | in-del | -/TGTTCTAAGTAGCT | | | intron-variant | YES1 | GRCh38.p7 | 18:785463 | TTGTTCTAAGTAGCT[-/TGTTCTAAGTAGCT]GGAAGGAGAGAGAAG | 7525 |
rs72204539 | in-del | -/AC | 0.411074 | 0.191194 | intron-variant | YES1 | GRCh38.p7 | 18:795913 | TATCCCAGAACTTAA[-/AC]ACACACACACACACA | 7525 |
rs72532196 | in-del | -/G | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722365 | TGCATGAAGTCCATC[-/G]TTCACATTTTAAAAA | 7525 |
rs72532197 | in-del | -/CTT | | | intron-variant | YES1 | GRCh38.p7 | 18:727598 | CTTTTTGTCTTYTCT[-/CTT]TSTTATTTTAGTAGT | 7525 |
rs72853881 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:741887 | ATTCCTTCCAAAGAG[C/T]GCCAGGTGCTTTGGG | 7525 |
rs72855238 | snp | C/T | 0.189261 | 0.242509 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:814257 | ACTTGTTTCCAGGAA[C/T]ATTTTTTAAAAAATT | 7525 |
rs72855240 | snp | A/T | 0.189576 | 0.242588 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:814265 | CCAGGAATATTTTTT[A/T]AAAAATTTTTTAATG | 7525 |
rs73370130 | snp | A/T | 0.0391387 | 0.134304 | intron-variant | YES1 | GRCh38.p7 | 18:726853 | TACTGTCAATAAATG[A/T]AAGGATTTCATACCT | 7525 |
rs73370137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:729964 | TCATCTCTTCCCTTC[C/T]TCATATATCTAGTAA | 7525 |
rs73370169 | snp | C/G | 0.0869089 | 0.189476 | intron-variant | YES1 | GRCh38.p7 | 18:748708 | TCATCTAGGTTATAG[C/G]ATGTCTATCAGTAGT | 7525 |
rs73370181 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | YES1 | GRCh38.p7 | 18:758740 | TATATACCATTTTTA[A/G]TTTACTGGTCAAATC | 7525 |
rs73372111 | snp | A/C | 0.0329836 | 0.124112 | intron-variant | YES1 | GRCh38.p7 | 18:773041 | GAAGGTACTATGATG[A/C]CTGGCCTCTTTAGCA | 7525 |
rs73372131 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | YES1 | GRCh38.p7 | 18:788310 | TGGGCTATAAAATGA[C/T]CATTTATATTCAGCT | 7525 |
rs73372137 | snp | G/T | 0.0825414 | 0.185628 | intron-variant | YES1 | GRCh38.p7 | 18:796316 | GTAAAAATAAAGATA[G/T]CAAGAATACTTAACT | 7525 |
rs73372150 | snp | A/T | 0.5 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:809244 | TAAAGAAAACGAACT[A/T]GAACTTTATTTAGAA | 7525 |
rs73372156 | snp | G/T | 0.139564 | 0.224285 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:812660 | CGTCCCTTCCCACCC[G/T]CGAACCCACCGACGC | 7525 |
rs73943168 | snp | C/T | 0.0256215 | 0.110247 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722539 | GTATTTTAAAACATA[C/T]ACACCAGACCTTCAT | 7525 |
rs73943186 | snp | G/T | 0.0232847 | 0.105357 | intron-variant | YES1 | GRCh38.p7 | 18:727221 | TGACCCTTTTATTAT[G/T]ATGAAACGTCCCTTT | 7525 |
rs73943187 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | YES1 | GRCh38.p7 | 18:727246 | CCCTTTTTGTCCCTA[G/T]TACTATTTCTTGCCT | 7525 |
rs73943188 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | YES1 | GRCh38.p7 | 18:727867 | GGCTTCCATATCTGA[C/G]GAAAAGTTAGCTGTC | 7525 |
rs73943189 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:733071 | CTCTACTGTAGTCAT[C/T]AGTGTCAATTCTTTA | 7525 |
rs73943191 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:739371 | GAGGCTGAGGTGGGA[C/G]GATCCTTTGAGCCAA | 7525 |
rs73943199 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | YES1 | GRCh38.p7 | 18:761051 | TTCCCAGTCTTCCAA[A/G]AAATGCACATTATAA | 7525 |
rs73945604 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | YES1 | GRCh38.p7 | 18:805225 | AACCTTGGGCCATAT[A/G]GTATGGCCTATTTCT | 7525 |
rs74336330 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | YES1 | GRCh38.p7 | 18:734895 | AGGTGTGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 7525 |
rs74401461 | snp | A/C | 0.5 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:787711 | TGAGACTCTGTCTCA[A/C]AAAAAAAAAAATATT | 7525 |
rs74463314 | snp | A/C | 0.5 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:745498 | GATATAAGGACCCAA[A/C]TGATGAGAGTCTATT | 7525 |
rs74476115 | snp | A/C | 0.5 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:787710 | GTGAGACTCTGTCTC[A/C]AAAAAAAAAAAATAT | 7525 |
rs74498689 | snp | G/T | 0.5 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:767130 | TTTTAAGCTAATTTT[G/T]GAATATATTATAATA | 7525 |
rs74540657 | snp | A/G | 0.243633 | 0.249919 | intron-variant | YES1 | GRCh38.p7 | 18:734641 | CAAATTAAAACTACA[A/G]TGAGACACTACCTTA | 7525 |
rs74589525 | snp | G/T | 0.5 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:781774 | ATTTCCTTTTTTTTT[G/T]GGAGGAATAATACCT | 7525 |
rs74664706 | snp | A/T | 0.5 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:754731 | AAAAAAAAAAAAAAA[A/T]CTCAGCTCAAATGAT | 7525 |
rs74729114 | snp | G/T | 0.0174175 | 0.0916809 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722355 | CACTGCCAACTTGCA[G/T]GAAGTCCATCTTCAC | 7525 |
rs74756964 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:784054 | TCCCCAAATTTCATA[C/G]TGGCAAAAAAATATT | 7525 |
rs74764242 | snp | A/G | 0.155656 | 0.231515 | intron-variant | YES1 | GRCh38.p7 | 18:797028 | ACATCATCTTCAAGT[A/G]GAGAAAATATTCTTG | 7525 |
rs74803845 | snp | C/T | 0.5 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:779910 | AATGTATGTAGTCCT[C/T]TTTTTTTTTTTTTCT | 7525 |
rs74864857 | snp | A/G | 0.155987 | 0.23165 | intron-variant | YES1 | GRCh38.p7 | 18:811090 | TTTAAAATTATCAAG[A/G]TATCTTTGGCACTGT | 7525 |
rs75039840 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:786364 | GGGAGCTTCACATAA[C/G]AGTGTCAAGTTTGAG | 7525 |
rs75092764 | snp | C/T | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:770269 | CCCGGCCCTTTTATC[C/T]TTTTTTTTTTTTTTT | 7525 |
rs75105448 | snp | C/T | 0.134119 | 0.221521 | intron-variant | YES1 | GRCh38.p7 | 18:767638 | TCATGTCAATGACGA[C/T]AGTCGTCATTACTGT | 7525 |
rs75113266 | snp | A/G | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:791274 | AAAGAAAAAAAAAAA[A/G]GAAAGTCTAGAAAGT | 7525 |
rs75156097 | snp | A/C | 0.5 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:771007 | AGATATCCCATCTCA[A/C]AAAAAAAAAAAAATC | 7525 |
rs75185628 | snp | C/T | 0.153997 | 0.230832 | intron-variant | YES1 | GRCh38.p7 | 18:806438 | GAATTAACTTCGAGC[C/T]ATGAAAAAGTATTAA | 7525 |
rs75214569 | snp | A/T | 0.5 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:754729 | AAAAAAAAAAAAAAA[A/T]ATCTCAGCTCAAATG | 7525 |
rs75320654 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | YES1 | GRCh38.p7 | 18:774700 | TAATTCAACAATACT[A/G]AATTATTCTAATAGC | 7525 |
rs75389570 | snp | C/T | 0.5 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:725513 | AACTATTAAAAAAAA[C/T]TCTACATGACATTAC | 7525 |
rs75488367 | snp | A/G | 0.5 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:791251 | GTGAAACTTGAAGAA[A/G]AAAAAAAAAAGAAAA | 7525 |
rs75525933 | snp | A/G | 0.0256215 | 0.110247 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:721645 | TTCTGCTCAGTAGTT[A/G]CAAGTAACTGAACAT | 7525 |
rs75537306 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | YES1 | GRCh38.p7 | 18:757036 | AAGCCCTACTCCAAT[C/T]GCTTCATTCTCCAAC | 7525 |
rs75540229 | snp | C/T | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:759707 | ACAATTTATTTATTT[C/T]TTTTTTTCTTTTATT | 7525 |
rs75588551 | snp | A/G | 0.234401 | 0.249513 | intron-variant | YES1 | GRCh38.p7 | 18:725330 | TCCTTCCCTGCCTGC[A/G]AGTCAGGCCATCCCT | 7525 |
rs75618678 | snp | G/T | 0.5 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:773850 | TCCCTTTTTTTTTTT[G/T]AGACGGAATCTTGCT | 7525 |
rs75634798 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:734029 | CACGCCTATAATCCC[A/C]GCAATTTGAGAGGCC | 7525 |
rs75640783 | in-del | -/AA | 0.190519 | 0.242821 | intron-variant | YES1 | GRCh38.p7 | 18:765236 | CTGGACAGGTTTGGG[-/AA]AGAGTTACAACTATA | 7525 |
rs75679646 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | YES1 | GRCh38.p7 | 18:791603 | AATACAAACCACATA[C/T]GCAATTTTAAATTTT | 7525 |
rs75701561 | snp | C/T | 0.242201 | 0.249878 | intron-variant | YES1 | GRCh38.p7 | 18:732308 | AGCTGGGTGTGGTGG[C/T]GGGTGCCTGTAATCC | 7525 |
rs75752288 | snp | A/G | 0.375 | 0.216506 | intron-variant | YES1 | GRCh38.p7 | 18:767349 | AGCCTAGGCAACATA[A/G]TGAAACCTCATCTCT | 7525 |
rs75774939 | snp | C/T | 0.277778 | 0.248452 | intron-variant | YES1 | GRCh38.p7 | 18:791868 | AGGGTTTCACCATGT[C/T]GGCCAAGCTGGTCTC | 7525 |
rs75822705 | snp | C/T | 0.104504 | 0.2033 | intron-variant | YES1 | GRCh38.p7 | 18:781378 | CTGTTTTCATAAACG[C/T]TTGGCACAACCTCCC | 7525 |
rs75872765 | snp | A/C | 0.5 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:728322 | ACAGAGACCCTGTCT[A/C]AAAAAAAAAAAAATT | 7525 |
rs75919468 | snp | A/G | 0.5 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:791275 | AAGAAAAAAAAAAAA[A/G]AAAGTCTAGAAAGTA | 7525 |
rs75977606 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:773849 | TTCCCTTTTTTTTTT[G/T]GAGACGGAATCTTGC | 7525 |
rs76014047 | snp | A/C | 0.375 | 0.216506 | intron-variant | YES1 | GRCh38.p7 | 18:736216 | AGATAGGAAGGCATT[A/C]CAGATGGAGGTAACT | 7525 |
rs76050640 | snp | A/G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:772563 | TCAGCCTCCTGAGTA[A/G/T]CTGGGATTACAGGCA | 7525 |
rs76054241 | snp | A/T | 0 | 0 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723395 | TTGTAAAACTTTCAC[A/T]TTCTTTTCTCGTATT | 7525 |
rs76143907 | snp | G/T | 0.5 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:809320 | TGACTTTTTTTTTTG[G/T]AGACAGTCTCACTCT | 7525 |
rs76153080 | snp | G/T | 0.242201 | 0.249878 | intron-variant | YES1 | GRCh38.p7 | 18:732157 | TAAAAAAATATACCA[G/T]GATGGGCACGGTGGC | 7525 |
rs76222387 | in-del | -/AT | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723393 | CTTGTAAAACTTTCA[-/AT]CWTTYTTTTCTCGTA | 7525 |
rs76243293 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:754489 | AGGCAGGCACATCCC[C/G]TAAATCAGGAGTTTA | 7525 |
rs76290917 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:782239 | GCCTTTTCGGCTCTT[A/C]ATAAGGTAAAACATG | 7525 |
rs76295281 | snp | A/T | 0.162142 | 0.235643 | intron-variant | YES1 | GRCh38.p7 | 18:789257 | GACCCAATACACTTA[A/T]GTCAAAGAGAGAACA | 7525 |
rs76360297 | snp | A/G | 0.234401 | 0.249513 | intron-variant | YES1 | GRCh38.p7 | 18:725794 | GGGAAGCTGAGGTGG[A/G]AGAATCACTTGAACG | 7525 |
rs76363818 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | YES1 | GRCh38.p7 | 18:741872 | CTGTTTGCAGTAGAC[A/C]TTCCTTCCAAAGAGC | 7525 |
rs76393975 | snp | C/T | 0.0850919 | 0.187897 | intron-variant | YES1 | GRCh38.p7 | 18:801495 | TACTGACAGGGCAAA[C/T]TAGAAAATGGCTATC | 7525 |
rs76419817 | snp | A/G | 0.234692 | 0.249531 | downstream-variant-500B | YES1 | GRCh38.p7 | 18:721487 | AGCTTGCAGTGAGCC[A/G]AGATCGCGCCACTGC | 7525 |
rs76425708 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | YES1 | GRCh38.p7 | 18:739926 | GCTTTTCAWTTTTTT[A/T]AAATTTTGTGCAGTT | 7525 |
rs76504598 | in-del | -/AAAAAA | | | intron-variant | YES1 | GRCh38.p7 | 18:777821 | TAAAAAAAAAAAAAA[-/AAAAAA]TTAAAAAAAGAATTA | 7525 |
rs76538127 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | YES1 | GRCh38.p7 | 18:803739 | GAGGGTGACTGGCAA[A/G]GCTACAGGTTCACCC | 7525 |
rs76639019 | snp | A/T | 0 | 0 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:814142 | CTCCCTTTTTTTTTT[A/T]ATTACTACATTCCCT | 7525 |
rs76650274 | snp | C/T | 0.155987 | 0.23165 | intron-variant | YES1 | GRCh38.p7 | 18:809954 | ATATATTTCCCTTCA[C/T]AGAACCACAGGTATT | 7525 |
rs76880270 | snp | A/G | 0.114036 | 0.209795 | intron-variant | YES1 | GRCh38.p7 | 18:746916 | TATGTGTGTGCATGT[A/G]TATATATACACATGT | 7525 |
rs76918191 | in-del | -/AA | | | intron-variant | YES1 | GRCh38.p7 | 18:791273 | AAAAGAAAAAAAAAA[-/AA]GAAAGTCTAGAAAGT | 7525 |
rs76944303 | snp | A/C | 0.0170251 | 0.090679 | intron-variant | YES1 | GRCh38.p7 | 18:732086 | TAGGTTAGAGAAATA[A/C]AACAAGAAAAGAATC | 7525 |
rs77081756 | snp | C/T | 0.5 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:779922 | CCTTTTTTTTTTTTT[C/T]TCTTAAATCTCTTTA | 7525 |
rs77284350 | snp | G/T | 0.154329 | 0.23097 | intron-variant | YES1 | GRCh38.p7 | 18:808321 | CTCTGAGTTTAGACA[G/T]GAGCTGGATGGTTAG | 7525 |
rs77409079 | snp | G/T | 0.5 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:769970 | TTCTTTTTTTTTTTT[G/T]GAGACGGAGTCTTGC | 7525 |
rs77494401 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:779325 | GGGAGGACAGCTTGA[C/G]CCTGGGAGGTCAAGG | 7525 |
rs77576435 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | YES1 | GRCh38.p7 | 18:728009 | TATACATAATGAGAT[A/G]TCTTAAGGGATGGGA | 7525 |
rs77690741 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | YES1 | GRCh38.p7 | 18:746767 | AGTAGTGTGTCACTG[A/C]AGGTGAATTTTTACT | 7525 |
rs77765790 | in-del | -/GAG | | | intron-variant | YES1 | GRCh38.p7 | 18:734466 | GGGAGGCTTAGGCAG[-/GAG]AATGGCGAGAACCCG | 7525 |
rs77803101 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | YES1 | GRCh38.p7 | 18:769523 | GAGGAAAGTATTTAG[C/T]CCATCACTATTATGT | 7525 |
rs77821257 | snp | A/C | 0.5 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:764121 | CGAGACTCCCTCTCA[A/C]AAAAAAAAAAAAAGA | 7525 |
rs77854655 | snp | A/C | 0.5 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:787709 | AGTGAGACTCTGTCT[A/C]AAAAAAAAAAAAATA | 7525 |
rs77878311 | snp | A/G | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:792567 | TCTCCCTCTGTATAT[A/G]TGTGTGTGTGTGTGT | 7525 |
rs77890744 | in-del | -/C | 0.199873 | 0.244923 | intron-variant | YES1 | GRCh38.p7 | 18:732165 | ATACCATGATGGGCA[-/C]CGGTGGCTCACGCCT | 7525 |
rs78112416 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:732300 | AAAAAATTAGCTGGG[C/T]GTGGTGGTGGGTGCC | 7525 |
rs78142911 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:739919 | CTTCTTAGCTTTTCA[A/T]TTTTTTTAAATTTTG | 7525 |
rs78214454 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | YES1 | GRCh38.p7 | 18:808187 | GTTCCAAGACAACAG[C/T]AGTGCTGCTGCAGCC | 7525 |
rs78380728 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | YES1 | GRCh38.p7 | 18:789747 | TAGGAGCAAACAAAA[C/T]TAGGAGAATTTACAA | 7525 |
rs78413827 | snp | A/G | 0.5 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:791252 | TGAAACTTGAAGAAG[A/G]AAAAAAAAAGAAAAA | 7525 |
rs78431783 | snp | C/T | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:770268 | GCCCGGCCCTTTTAT[C/T]TTTTTTTTTTTTTTT | 7525 |
rs78432246 | snp | G/T | 0.5 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:793058 | GTTTTTTTTTTTTTT[G/T]GAGACAGAGTCTCAC | 7525 |
rs78515215 | snp | C/G | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:731945 | GCACTCCAGCCTGGG[C/G]GACAGAGCGAGACTC | 7525 |
rs78575837 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:782438 | TCCCACCTGAACCAT[C/G]AGATGATAGGAAAGG | 7525 |
rs78634036 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | YES1 | GRCh38.p7 | 18:794535 | CTTGCCACATTTCCT[C/T]TATTGTTCCCTCCTA | 7525 |
rs78826733 | snp | G/T | 0.5 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:772449 | TTTTTTCTTTTTTTT[G/T]GAGATAGAGTCTCAC | 7525 |
rs79060968 | snp | A/G | 0.5 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:738488 | GAGGTCAGGAGATCA[A/G]GACCATCCTGGCGAA | 7525 |
rs79116792 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:775598 | GCCCAGGAGTTTGAG[A/G]CCACCCTGAGCAACA | 7525 |
rs79218339 | snp | C/T | 0 | 0 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:812547 | TCACTTCTCCCGACC[C/T]AACATGGCGGCGGGG | 7525 |
rs79237950 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | YES1 | GRCh38.p7 | 18:774191 | CTTACTGGCTGCTCC[G/T]TCTCAGTCTCCTTTG | 7525 |
rs79327231 | snp | A/C | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:728325 | GAGACCCTGTCTCAA[A/C]AAAAAAAAAATTCAT | 7525 |
rs79416929 | snp | A/G | 0.155325 | 0.23138 | intron-variant | YES1 | GRCh38.p7 | 18:803672 | TGAGTCTCCTAACAG[A/G]GAACTCAAAACAGTG | 7525 |
rs79468730 | snp | A/G | 0.15698 | 0.23205 | intron-variant | YES1 | GRCh38.p7 | 18:811721 | AGACCCCCAGCCTTT[A/G]GGACCCAAAGGGGCC | 7525 |
rs79525137 | snp | A/T | 0.5 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:734404 | CTAAAAATACAAAAA[A/T]AAAAATTAGCCGAGC | 7525 |
rs79559730 | snp | A/C | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:725512 | AAACTATTAAAAAAA[A/C]CTCTACATGACATTA | 7525 |
rs79564753 | snp | A/G | 0.5 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:784033 | CAGGCATAATACGAC[A/G]GAATTTCCCCAAATT | 7525 |
rs79610931 | in-del | -/AAA | | | intron-variant | YES1 | GRCh38.p7 | 18:761257 | TAAAAAAAAAAAAAA[-/AAA]GTTTAACTGTAAAAA | 7525 |
rs79660941 | snp | A/T | 0.469148 | 0.120308 | intron-variant | YES1 | GRCh38.p7 | 18:730961 | GAGAAGGGTGAAATC[A/T]GCAAAGGAGTGATTA | 7525 |
rs79699521 | snp | A/C | 0.122064 | 0.214785 | intron-variant | YES1 | GRCh38.p7 | 18:786293 | TTCCTTCTTTGTCAC[A/C]ATATCAAACATGGAG | 7525 |
rs79830204 | in-del | -/AAA | | | intron-variant | YES1 | GRCh38.p7 | 18:777833 | AAAAAAAAATTAAAA[-/AAA]GAATTACCTATATCA | 7525 |
rs79927192 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | YES1 | GRCh38.p7 | 18:808958 | AAAAACTAAGGCTGA[A/T]ATTACTGATCTAAAG | 7525 |
rs79946736 | snp | C/G | 0.0287284 | 0.116357 | intron-variant | YES1 | GRCh38.p7 | 18:770470 | TGTATGTTCATTCTA[C/G]AATTCAGCAAAAAGT | 7525 |
rs79964049 | snp | A/G | 0.15665 | 0.231917 | intron-variant | YES1 | GRCh38.p7 | 18:803679 | CCTAACAGGGAACTC[A/G]AAACAGTGATTTTTA | 7525 |
rs80050365 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:731835 | AGCTGGGCGTGGTGG[C/T]GGGTGCCTATAGTCC | 7525 |
rs80130545 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:775969 | GGTAAGGGATATGAA[A/T]TGTTTCCAGTTTTTT | 7525 |
rs80144518 | snp | A/T | 0.155325 | 0.23138 | intron-variant | YES1 | GRCh38.p7 | 18:804265 | TGTTAACTGACATCA[A/T]AACTATCCACTTCAA | 7525 |
rs80161838 | snp | A/T | 0.5 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:783420 | ACACACACGGAAAAA[A/T]TAATCACATAACCTA | 7525 |
rs111232601 | snp | A/G | 0.5 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:801133 | CCTGGGCAACAGAGC[A/G]AGACTCCATCTCAAA | 7525 |
rs111232778 | snp | A/T | 0.5 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:727028 | AAAATCGTCAAAGAA[A/T]GACAATGAATGATAA | 7525 |
rs111283766 | snp | A/C | 0.5 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:769752 | AGTAAACCTTGGGAC[A/C]TTTGCATTCTTGAGA | 7525 |
rs111294503 | snp | C/T | 0.5 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:798363 | TCATTGTAAAAATCC[C/T]ATTCATCTTCTGACA | 7525 |
rs111294651 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | YES1 | GRCh38.p7 | 18:731839 | GGGCGTGGTGGCGGG[C/T]GCCTATAGTCCTAGC | 7525 |
rs111361288 | snp | C/T | 0.0839998 | 0.186933 | intron-variant | YES1 | GRCh38.p7 | 18:764010 | CTGTAGTCCCAGCTA[C/T]TCGGGAGGCTGAGGC | 7525 |
rs111403508 | snp | C/T | 0.15665 | 0.231917 | intron-variant | YES1 | GRCh38.p7 | 18:783899 | GATTACAGGTGTGAA[C/T]CACCGCACCTAGCTC | 7525 |
rs111416313 | snp | C/T | 1.65688e-05 | 0.00287821 | missense | YES1 | GRCh38.p7 | 18:751793 | ATAAGGCCACAAATA[C/T]AGTAACACCACCTAT | 7525 |
rs111492845 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:789988 | GCTTGAACCAGGGAG[A/G]TTGAGGATGCAGTGA | 7525 |
rs111521728 | snp | G/T | 0.030278 | 0.119257 | intron-variant | YES1 | GRCh38.p7 | 18:779990 | TGTAATCCCAGCACT[G/T]TGGGAGGCTGAGGAG | 7525 |
rs111542039 | snp | A/G | 0.135825 | 0.222405 | utr-variant-5-prime | YES1 | GRCh38.p7 | 18:812169 | GCTCGAGGTGGCGGA[A/G]GGCGGAGGCGAGGCC | 7525 |
rs111578682 | snp | A/G | 0.0287735 | 0.116442 | intron-variant | YES1 | GRCh38.p7 | 18:756859 | ACAATAAAATATTTT[A/G]AGAGTCAGTTAACAC | 7525 |
rs111612318 | snp | C/T | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:787345 | CTCAGGTGGTCCGCC[C/T]GCCTCGGCCTCCCAA | 7525 |
rs111615362 | snp | C/T | 0.5 | 0 | downstream-variant-500B | YES1 | GRCh38.p7 | 18:721303 | AGCACTTTGGGAGGC[C/T]GAAGCGGACGGATCA | 7525 |
rs111747768 | snp | C/T | 0.155325 | 0.23138 | intron-variant | YES1 | GRCh38.p7 | 18:811927 | GGCGAGCAGGTAGCG[C/T]GGGGAACGAGACAAG | 7525 |
rs111790871 | in-del | -/A | 0.5 | 0 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:775806 | TGCCTCAAATAAATT[-/A]AAAAAAAAAATAGAA | 7525 |
rs111830997 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | YES1 | GRCh38.p7 | 18:749568 | TTATAAAAATGTTAT[C/T]TAGAAGGCTGGGCGC | 7525 |
rs111876808 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | YES1 | GRCh38.p7 | 18:811523 | AACGGGAGGCGGAGT[A/G]GCATGATTCCGTAAA | 7525 |
rs111973701 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | YES1 | GRCh38.p7 | 18:753631 | GCTGGGATTACAGGC[A/G]TGCACCTCCACGCCC | 7525 |
rs112072774 | snp | A/G | 0.5 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:751001 | GTTGTTATCATTGTC[A/G]TTTTCCTTTTATCTT | 7525 |
rs112082973 | snp | C/G | 0.0858192 | 0.188533 | intron-variant | YES1 | GRCh38.p7 | 18:764763 | TTTGAGACGGAGTCT[C/G]GTTCTGTCACCCAGG | 7525 |
rs112129280 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | YES1 | GRCh38.p7 | 18:759389 | GGAGAATTGCTTGAA[C/T]CCAGGAGGCGGAGGT | 7525 |
rs112163023 | snp | C/T | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:766144 | TTACGTTTGCCAAGT[C/T]CTTCAGGGGAGGCTC | 7525 |
rs112231914 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:729649 | TTTTTTTTTTTGAGA[C/G]AGAGTCTCGCTCTGT | 7525 |
rs112310556 | snp | A/G | 0.5 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:774118 | TTACGGGCTTAAGCC[A/G]CGGCGCCTGGCCTTC | 7525 |
rs112328437 | snp | C/T | 0.155325 | 0.23138 | intron-variant | YES1 | GRCh38.p7 | 18:811574 | TTTCCCAACCCCCAA[C/T]CCAAAACAAAGGAAA | 7525 |
rs112339037 | snp | A/G | 0.5 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:765237 | TGGACAGGTTTGGGA[A/G]AGAGTTACAACTATA | 7525 |
rs112390855 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:769916 | TTTGGTATCAGGATG[C/T]TGGCCTCACAAAATG | 7525 |
rs112440143 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | YES1 | GRCh38.p7 | 18:728462 | CTGTCACATGAGGAC[A/G]GGTGTGGAATTTTCC | 7525 |
rs112462503 | snp | C/G | 0.114387 | 0.210022 | intron-variant | YES1 | GRCh38.p7 | 18:725859 | ATAGCACTCCAGCCT[C/G]GGTGACAGAGCGAGA | 7525 |
rs112481414 | snp | A/C | | | intron-variant | YES1 | GRCh38.p7 | 18:763374 | GTTAGACAAGTTATA[A/C]AACTATTCCAACTGA | 7525 |
rs112591747 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | YES1 | GRCh38.p7 | 18:796956 | ATAAAATCCAGAGTA[C/T]AGAGCTAAATGACTT | 7525 |
rs112601504 | snp | C/T | 0.15665 | 0.231917 | intron-variant | YES1 | GRCh38.p7 | 18:785207 | ATTGTATTTTATGTG[C/T]GGCCCAAGATAATTC | 7525 |
rs112601649 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | YES1 | GRCh38.p7 | 18:808714 | AGATCTCTTCTTCAA[C/T]TCTACAACAATGCAA | 7525 |
rs112605495 | snp | A/G | 0.5 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:754435 | CTCAAGGCTGGGTGC[A/G]GTGGCTCACGCATGT | 7525 |
rs112610510 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | YES1 | GRCh38.p7 | 18:800991 | TCTCTACTAAAAATA[C/T]AAAAATTAGCTGGGT | 7525 |
rs112614283 | snp | G/T | 0.0209421 | 0.100162 | intron-variant | YES1 | GRCh38.p7 | 18:809573 | CCTAAAGTGCTGGGA[G/T]TACAGGTGTGAGCCA | 7525 |
rs112622843 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | YES1 | GRCh38.p7 | 18:755201 | TAACATGCATAACTC[C/T]CTAAATGAAGTCTAA | 7525 |
rs112642269 | snp | A/G | 0.130351 | 0.219509 | intron-variant | YES1 | GRCh38.p7 | 18:759371 | ACTTGGGAGGCTGGC[A/G]CAGGAGAATTGCTTG | 7525 |
rs112660515 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:730363 | TTTTTTTTTTTTTTT[C/G]AGACAGGGTCTTGCT | 7525 |
rs112667246 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | YES1 | GRCh38.p7 | 18:734434 | CTTGGTGGCAGGCAC[C/G]TGTAGTCCCAGCTAC | 7525 |
rs112780461 | snp | C/G | 0.444444 | 0.157135 | intron-variant | YES1 | GRCh38.p7 | 18:745565 | TATTACCTGTTCCTC[C/G]CTTTAGAATACAACA | 7525 |
rs112780479 | snp | C/T | 0.0509478 | 0.151255 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723394 | CTTGTAAAACTTTCA[C/T]TTTCTTTTCTCGTAT | 7525 |
rs112827725 | snp | A/G | 0.5 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:734229 | GGTTGCAGTGAGCCA[A/G]GATCATGCCACTTCA | 7525 |
rs112855601 | snp | A/T | 0.00438332 | 0.0466095 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:721690 | AAGAATAAATTCAGA[A/T]TATATCAGTTTTTAA | 7525 |
rs112857658 | snp | A/G | 0.243633 | 0.249919 | intron-variant | YES1 | GRCh38.p7 | 18:734752 | TTTTCCACTGATGGT[A/G]GGAATGTAAATTAGT | 7525 |
rs112925617 | snp | A/G | 0.031825 | 0.122064 | intron-variant | YES1 | GRCh38.p7 | 18:753167 | GGTTAAAAACTCCAT[A/G]ATATATTAATATTCT | 7525 |
rs113016224 | snp | A/C | 0.5 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:750304 | ACTGAATACCTATTA[A/C]GTGACAGACTTTAGA | 7525 |
rs113130126 | snp | C/T | 0.5 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:754665 | TGCAGTGAGCCAAGA[C/T]TGCGCCACTGCACTC | 7525 |
rs113163956 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | YES1 | GRCh38.p7 | 18:781007 | GGGGCGGTGGCTCAC[A/G]CCTTCAATCCCAGCA | 7525 |
rs113216314 | snp | A/G | 0.5 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:751442 | AAATAATACACTTGC[A/G]TGTACTCCCCTCAGT | 7525 |
rs113252640 | snp | A/G | 0.0818113 | 0.184966 | intron-variant | YES1 | GRCh38.p7 | 18:802863 | TGAGGCAAGTGGATC[A/G]CTTGAGCCCAGGAGT | 7525 |
rs113297374 | in-del | -/AG | 0.5 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:793064 | TTTTTTTTTTGAGAC[-/AG]AGTCTCACTGTGTCA | 7525 |
rs113322268 | snp | A/C | 0.0287284 | 0.116357 | intron-variant | YES1 | GRCh38.p7 | 18:801584 | ATTTCTACTAACTCA[A/C]CTAGAAATAAATGAT | 7525 |
rs113404360 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:776343 | GGATTACAGGCTCAT[A/G]CCACCACGCCTGGCC | 7525 |
rs113438318 | snp | C/G | 0.0376037 | 0.131863 | downstream-variant-500B | YES1 | GRCh38.p7 | 18:721280 | CGGTGGCTCACGCCT[C/G]TAATCCCAGCACTTT | 7525 |
rs113473174 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | YES1 | GRCh38.p7 | 18:811764 | CCTACTTCGGCCGTA[A/G]GGGCAAAAATAAACC | 7525 |
rs113593987 | in-del | -/GCTTGTTCTAAGTA | 0.0926964 | 0.194308 | intron-variant | YES1 | GRCh38.p7 | 18:785446 | AACAAGTAAAGCTGG[-/GCTTGTTCTAAGTA]GCTTGTTCTAAGTAG | 7525 |
rs113607854 | snp | A/C | 0.0240643 | 0.107019 | intron-variant | YES1 | GRCh38.p7 | 18:811778 | AGGGGCAAAAATAAA[A/C]CTCTCCTCCCCGTCG | 7525 |
rs113672630 | snp | C/T | 0.5 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:762966 | TGTTATCAGCTCTGC[C/T]TAAAGCACTTAGGAA | 7525 |
rs113690374 | in-del | -/T | 0 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:810009 | GAATTTCCTTGCAGG[-/T]TTTTTTTTTTTTTTT | 7525 |
rs113767987 | snp | A/G | 0.0115144 | 0.0749975 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:813033 | AGCCTTGCCGGGAGG[A/G]GAACCGAAGCTGAGT | 7525 |
rs113811708 | snp | G/T | 0.132409 | 0.220618 | intron-variant | YES1 | GRCh38.p7 | 18:764152 | AAAAGTCATTCATTC[G/T]TCAGTATTTATTGAA | 7525 |
rs113819660 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | YES1 | GRCh38.p7 | 18:739552 | AGGCTCTTCAAGCAC[G/T]GAGCTATCAGTGCAC | 7525 |
rs113912442 | snp | A/G | 0.5 | 0 | intron-variant | YES1 | GRCh38.p7 | 18:751634 | TCTGGATCATCAACC[A/G]GCTCAGTGGTTCCTG | 7525 |
rs113970832 | snp | A/G | 0.143622 | 0.226238 | intron-variant | YES1 | GRCh38.p7 | 18:764107 | CCTGGGCGACAGAGC[A/G]AGACTCCCTCTCAAA | 7525 |
rs114039991 | snp | C/G/T | 0.0193772 | 0.0965046 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:724360 | TTCTTTTGATTCCTG[C/G/T]AGAAAATCTACACAA | 7525 |
rs114056355 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | YES1 | GRCh38.p7 | 18:805780 | AGAAGTCAATACATT[C/T]GCCAGGAAACAATGT | 7525 |
rs114064729 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | YES1 | GRCh38.p7 | 18:754603 | GTTATCTCAGCTACT[C/T]GGGAGGCTAAGGCAA | 7525 |
rs114094942 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | YES1 | GRCh38.p7 | 18:774501 | CAATCTTCCCCAACT[C/T]GATAAATGTTAACGC | 7525 |
rs114168210 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | YES1 | GRCh38.p7 | 18:810625 | GTTTTGTTTTCAGAT[A/C]AAAGGCAATTGTCTT | 7525 |
rs114193072 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | YES1 | GRCh38.p7 | 18:799871 | GCCTGGGCTAAAGAA[C/T]GAGACTCTGTCTCAA | 7525 |
rs114266674 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | YES1 | GRCh38.p7 | 18:761397 | TTGTATGAAGGAGGA[A/G]AAATTATGGGGGAAA | 7525 |
rs114385864 | snp | A/T | 0.0182019 | 0.0936463 | intron-variant | YES1 | GRCh38.p7 | 18:797089 | CATTATGCACAGACA[A/T]GGAAAAGTCTTTGCA | 7525 |
rs114426881 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | YES1 | GRCh38.p7 | 18:735791 | GGTGCACTGAAATCA[A/C]CACTAAAGAACTAGT | 7525 |
rs114450270 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | YES1 | GRCh38.p7 | 18:728021 | GATATCTTAAGGGAT[A/G]GGACCCAAGTCTAAA | 7525 |
rs114470996 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | YES1 | GRCh38.p7 | 18:796664 | CTCAGTTGCTGAGGC[A/G]GGAGAATCACTTGAA | 7525 |
rs114510419 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | YES1 | GRCh38.p7 | 18:785600 | ACCCAAAGTTCACGT[A/G]TTGGAAGCTTAATCC | 7525 |
rs114578330 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | YES1 | GRCh38.p7 | 18:792618 | ATATATACATACATA[C/T]ATATACGCACACACA | 7525 |
rs114582122 | snp | A/T | 0.0345262 | 0.126772 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:812596 | GGGCGGTGCAGGCCG[A/T]GGGGGCGTGAGGAGG | 7525 |
rs114591359 | snp | A/G | 0.0535932 | 0.154675 | intron-variant | YES1 | GRCh38.p7 | 18:789320 | GGCATGGTGACTCAC[A/G]CATGTAATCCCAACA | 7525 |
rs114633786 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | YES1 | GRCh38.p7 | 18:746229 | AATATCACAAATATT[A/C]CTGTTAGAATATACT | 7525 |
rs114670339 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | YES1 | GRCh38.p7 | 18:805787 | AATACATTCGCCAGG[A/G]AACAATGTGAAGTAT | 7525 |
rs114701862 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | YES1 | GRCh38.p7 | 18:727129 | TTAACTAGAATATCC[C/T]GATCATATAAATTTT | 7525 |
rs114740824 | snp | A/T | 0.00499183 | 0.0497091 | intron-variant | YES1 | GRCh38.p7 | 18:742891 | AACATTATCAACACA[A/T]ATACCTAAGGAGATA | 7525 |
rs114741143 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:805848 | CACCTCACCCCAATT[C/T]CTACTTAATGCTAAG | 7525 |
rs114747150 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | YES1 | GRCh38.p7 | 18:753403 | TCCTCCTATCTAAAT[G/T]TTGTATCCTTTAGCC | 7525 |
rs114764425 | snp | A/G | 0.00398564 | 0.0444627 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:724224 | TGGACCCTGAAATAC[A/G]CTGATAAATTCATCA | 7525 |
rs114826826 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | YES1 | GRCh38.p7 | 18:742335 | ATTGAAGGTAGTGGG[A/G]AGGCCAGGCACAGTG | 7525 |
rs114843162 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | YES1 | GRCh38.p7 | 18:772358 | TGAATGCAGGTCTTG[A/G]TACTAGGTAAACATT | 7525 |
rs114856874 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | YES1 | GRCh38.p7 | 18:774398 | ACTTTTAACTGTCTA[C/T]GCAATACCTTCACTT | 7525 |
rs114858705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:800119 | GAGCGTTAATGATAC[C/T]AGTTTAGCACAAGTC | 7525 |
rs114869791 | snp | G/T | 0.0581099 | 0.160244 | intron-variant | YES1 | GRCh38.p7 | 18:767626 | ACATATCTATTCTCA[G/T]GTCAATGACGATAGT | 7525 |
rs114941912 | snp | C/G | 0.0197687 | 0.0974348 | intron-variant | YES1 | GRCh38.p7 | 18:737522 | CTTCTTGTGTCTGTG[C/G]TTAGGAGAAGAGGTA | 7525 |
rs114970610 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | YES1 | GRCh38.p7 | 18:803091 | AAAAAAAATTAGCTG[C/G]GCATGGTGGCTCACA | 7525 |
rs114984545 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | YES1 | GRCh38.p7 | 18:794357 | ACTTTTAAAAATATC[A/T]ATGTCATGAAAGATA | 7525 |
rs115041214 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | YES1 | GRCh38.p7 | 18:811752 | GCTTCCCTCGCCCCT[A/G]CTTCGGCCGTAGGGG | 7525 |
rs115046804 | snp | A/T | 0.0333695 | 0.124785 | intron-variant | YES1 | GRCh38.p7 | 18:788354 | GATGACCTAAAAATT[A/T]AAACCAGAACTTCGT | 7525 |
rs115199938 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | YES1 | GRCh38.p7 | 18:781653 | TATTTTTACAGATCA[C/T]GAATACAAACTGACT | 7525 |
rs115215517 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | YES1 | GRCh38.p7 | 18:803329 | TGTGATAATGCATAT[A/G]AAAGTATGGCATAGC | 7525 |
rs115237586 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | YES1 | GRCh38.p7 | 18:737936 | TGTTGCCCAGGCCCC[A/G]CAAAGCGAGATTATA | 7525 |
rs115288319 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:775623 | GCAACATAATGAGAC[C/T]TCATCTCTACAAAAA | 7525 |
rs115311992 | snp | C/T | 0.00358779 | 0.0422022 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723263 | TTAGTTTTATAGTTA[C/T]ACTTTATAACTCTTC | 7525 |
rs115313702 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | YES1 | GRCh38.p7 | 18:789451 | AGCCAAGTGTGGTAG[C/T]ACAGGCCTGTAGTCC | 7525 |
rs115329060 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | YES1 | GRCh38.p7 | 18:805952 | ACATTTTGCTGGGAA[C/T]AGAGGCTGAAAACCA | 7525 |
rs115332724 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | YES1 | GRCh38.p7 | 18:783337 | CATCCTAAATGTCTT[C/T]TCAAAATCTTGTTCC | 7525 |
rs115365582 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | YES1 | GRCh38.p7 | 18:754999 | AATAGAATATTTCAT[A/G]TAAGTAAATTGCTTT | 7525 |
rs115371231 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | YES1 | GRCh38.p7 | 18:808639 | ACAAAGCGTGCACCA[C/T]AAACATCACCTTTAT | 7525 |
rs115421340 | snp | C/T | 0.113685 | 0.209567 | intron-variant | YES1 | GRCh38.p7 | 18:728774 | CGTGATCCACTGGCC[C/T]CGACCTCCCAAAGTA | 7525 |
rs115546519 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | YES1 | GRCh38.p7 | 18:766031 | ACTGATCCTCTACTT[C/T]ACAGTATTAGTGTAA | 7525 |
rs115552089 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | YES1 | GRCh38.p7 | 18:798345 | CCTTTTCTGAAACAT[C/T]GGTCATTGTAAAAAT | 7525 |
rs115564298 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | YES1 | GRCh38.p7 | 18:742720 | TTCAGCCTGCCTACT[C/T]TTCCTTTTAAACGTC | 7525 |
rs115585926 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | YES1 | GRCh38.p7 | 18:800416 | GGTACAACAGCAGTT[C/T]GAAACCTATCTGCCA | 7525 |
rs115669917 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | YES1 | GRCh38.p7 | 18:725046 | AAAGTTCTAGTCTTG[C/G]TTTTGCCAAATATAC | 7525 |
rs115670803 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | YES1 | GRCh38.p7 | 18:774106 | AAAGTGCTGGGATTA[C/T]GGGCTTAAGCCACGG | 7525 |
rs115716158 | snp | A/G | 0.030278 | 0.119257 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:775251 | CATTTTGATAATGGT[A/G]GCTCTCTTCCACAGC | 7525 |
rs115737875 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | YES1 | GRCh38.p7 | 18:804184 | AATTAAATGTAAATT[C/T]TGATGATAGTGGCTA | 7525 |
rs115828576 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | YES1 | GRCh38.p7 | 18:784165 | AATGTCTAATTTATT[A/C]TCATATTTAAGAAGA | 7525 |
rs115854277 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | YES1 | GRCh38.p7 | 18:795987 | AGTTCAGAGTCTATA[C/T]AATAAAACTGGGATA | 7525 |
rs115854297 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | YES1 | GRCh38.p7 | 18:737601 | TATCAGGCACAACCT[A/G]AGATGACATGGTGAT | 7525 |
rs115892045 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | YES1 | GRCh38.p7 | 18:763676 | GCCACTGCACTCCAT[C/T]CTGGATGACAGAGGA | 7525 |
rs115919006 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | YES1 | GRCh38.p7 | 18:745611 | TGTATTATGTGTAAA[C/T]AAGTGTGTTAAATCT | 7525 |
rs115970340 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | YES1 | GRCh38.p7 | 18:784563 | CCGGTGTCCCTGGAC[A/T]AAAATCAAGGTGTCA | 7525 |
rs116004625 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | YES1 | GRCh38.p7 | 18:748602 | TCTCTATGGATATGC[C/T]CACTGCATGCACCTT | 7525 |
rs116006720 | snp | A/G | 0.00993419 | 0.0697739 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723502 | ATATTTTCTATTTGT[A/G]GCACCCATCCCCATA | 7525 |
rs116151031 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | YES1 | GRCh38.p7 | 18:767567 | AGCAATTAACCATGT[A/G]TGTGTGTAGGTCTGC | 7525 |
rs116178269 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | YES1 | GRCh38.p7 | 18:784990 | ATCAGTATACTACAA[C/T]AATCATGCTCATGCT | 7525 |
rs116207186 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | YES1 | GRCh38.p7 | 18:801534 | ACACGTCTGAAATTT[C/T]AACTGAACCATCAGG | 7525 |
rs116246620 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | YES1 | GRCh38.p7 | 18:777989 | CAGTGTTACACTGTT[A/C]AAGTATTTTGCTTTA | 7525 |
rs116247307 | snp | G/T | 0.00199481 | 0.0315187 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722325 | AAAAACAACCACAAT[G/T]TTTAGTACCAGAACC | 7525 |
rs116262366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:789993 | AACCAGGGAGGTTGA[A/G]GATGCAGTGAGCTGA | 7525 |
rs116305806 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | YES1 | GRCh38.p7 | 18:806252 | ACTAAAATAGTACAA[C/T]GTATTTATTTAAAAT | 7525 |
rs116319430 | snp | C/T | 0.00914312 | 0.0669923 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:813378 | GCAGTCACTTTTGCC[C/T]TATCAGACTTTTAGA | 7525 |
rs116408336 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | YES1 | GRCh38.p7 | 18:731352 | AGGAGTTTTGTTGGA[C/G]AGGACAATGGTGAGT | 7525 |
rs116447670 | snp | C/T | 0.030278 | 0.119257 | intron-variant | YES1 | GRCh38.p7 | 18:793637 | CCACTGTGTCTGACC[C/T]GCATGATCCCTTATA | 7525 |
rs116449434 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | YES1 | GRCh38.p7 | 18:744811 | ATTAAAGGCACAATC[A/C]ACATGCCTAACAGGA | 7525 |
rs116450498 | snp | C/G | 0.029116 | 0.117091 | intron-variant | YES1 | GRCh38.p7 | 18:736245 | CTGTACAGAAGTATG[C/G]AGGTTGAAAGAAAGC | 7525 |
rs116463618 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | YES1 | GRCh38.p7 | 18:770030 | GTGATCCCGGCTCAC[C/T]GCAACTGCAATCTCT | 7525 |
rs116465254 | snp | C/T | 0.021333 | 0.101051 | intron-variant | YES1 | GRCh38.p7 | 18:761770 | CCCAGTATCAATGCA[C/T]AGGACCCATCATTGC | 7525 |
rs116506649 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | YES1 | GRCh38.p7 | 18:727619 | TTTTAGTAGTTATCA[C/T]TGAGACTACAATATG | 7525 |
rs116519574 | snp | A/C | 0.0372196 | 0.131242 | intron-variant | YES1 | GRCh38.p7 | 18:803466 | TATTGTAACACTCCT[A/C]ATTTTCCCAAACCCT | 7525 |
rs116560648 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | YES1 | GRCh38.p7 | 18:772827 | TTTCTACTTACTCAT[A/G]ATTTTTATTCATTTG | 7525 |
rs116560809 | snp | A/G | 0.00755907 | 0.0610114 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:813095 | TTTGGCTTATGTTGG[A/G]ACAGCGTTTTTCTAT | 7525 |
rs116562117 | snp | C/T | 0.029116 | 0.117091 | intron-variant | YES1 | GRCh38.p7 | 18:764189 | AAAGTACTTACTATA[C/T]GTGTATTAAGGGTTG | 7525 |
rs116576441 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | YES1 | GRCh38.p7 | 18:785493 | GAAGGAGAGAGAAGC[A/G]CTATAAAAGGTCTGA | 7525 |
rs116649399 | snp | A/G | 0.0349115 | 0.127424 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:724330 | TTAAAAACATGCAGA[A/G]TAAAGAAGATTTTCT | 7525 |
rs116663455 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:738277 | AATACCTACCACATA[A/T]CTGAAGAGAAACTTT | 7525 |
rs116672412 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | YES1 | GRCh38.p7 | 18:788032 | GAAAGGCAGGATGCA[C/T]GCTGACTGTTTCCAG | 7525 |
rs116702846 | snp | C/G | 0.0535932 | 0.154675 | intron-variant | YES1 | GRCh38.p7 | 18:802507 | GGAGACCACACTATT[C/G]CACCCCAGCCTGGGC | 7525 |
rs116774977 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | YES1 | GRCh38.p7 | 18:809987 | ATGCTTCTATTTTTA[C/T]GTTCACAGAATTTCC | 7525 |
rs116775236 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | YES1 | GRCh38.p7 | 18:758551 | AAAATTGTCTCTGTT[A/C]CAAGTATTCTCCCCA | 7525 |
rs116807790 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | YES1 | GRCh38.p7 | 18:778429 | GTCAGCATGACAATG[C/T]TGCCTTATTATTAGT | 7525 |
rs116857644 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:744339 | CACTAATTTGTAAGA[A/G]GCATACCAAAAAATC | 7525 |
rs116911862 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | YES1 | GRCh38.p7 | 18:755834 | AGCCAGCTATACTTT[A/G]TTACTTCAGTGAAAA | 7525 |
rs116923188 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | YES1 | GRCh38.p7 | 18:806180 | TACTGTGATGAGATA[C/G]CAAATGCATTTTTTA | 7525 |
rs116990357 | snp | A/C/T | 0.00239393 | 0.0345281 | intron-variant | YES1 | GRCh38.p7 | 18:751380 | TTACACCATCTGGTA[A/C/T]TTAGAAAAATAGGAG | 7525 |
rs117002915 | snp | A/G | 0.157972 | 0.232445 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:812689 | GCTCGGCTGCCGCGG[A/G]GATTGAATGGAGCGC | 7525 |
rs117115981 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | YES1 | GRCh38.p7 | 18:728893 | GTTTGGCTTTGATTT[C/T]TGTAATTTGACCATG | 7525 |
rs117136965 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | YES1 | GRCh38.p7 | 18:750024 | AATAGGAAGATAGAT[A/G]TGGGATTTGTTACTA | 7525 |
rs117299658 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | YES1 | GRCh38.p7 | 18:782310 | TAGGCTGAGGAACCA[C/T]AAAATATCAATTCCT | 7525 |
rs117449313 | snp | G/T | 0.0108545 | 0.0728659 | missense | YES1 | GRCh38.p7 | 18:751739 | ATCTTTCACCCTTCT[G/T]AAATGAAAGGTCTTC | 7525 |
rs117512062 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | YES1 | GRCh38.p7 | 18:808262 | AGCACTGGCTCTTCT[C/T]TTTCACCCTCTACTG | 7525 |
rs117545986 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | YES1 | GRCh38.p7 | 18:800498 | GTACTGTAGATATTG[A/T]GGGATAATAATGCTA | 7525 |
rs117638639 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | YES1 | GRCh38.p7 | 18:802244 | AACACAGCAAGACCA[C/T]CTCTCTTAAAAAAGA | 7525 |
rs117675380 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | YES1 | GRCh38.p7 | 18:811671 | CACACCCGCTCCTCT[C/T]CCCGCACAGCTGCTA | 7525 |
rs117682421 | snp | C/G | 0.0240643 | 0.107019 | intron-variant | YES1 | GRCh38.p7 | 18:802790 | ATCTGTAATAAATAC[C/G]TACCTCAAGGGGCCC | 7525 |
rs117853570 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:798855 | TTAAAATCCAGAACT[A/G]TCTTTCCTGCTACTT | 7525 |
rs117881436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:777012 | AGGCCAATTAGACAT[C/T]AACCACAAAAATCAG | 7525 |
rs117959130 | snp | A/T | 0.02016 | 0.0983543 | intron-variant | YES1 | GRCh38.p7 | 18:762633 | ATACATTATGGGATT[A/T]AAAAAAACTATATAC | 7525 |
rs118120624 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | YES1 | GRCh38.p7 | 18:809598 | GAGCCACCGTGCCCA[A/G]CCTGACGTGTTCAAA | 7525 |
rs137885192 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:776279 | GCTCACTGCAACCTC[C/T]GCCTCTGGGGTTCAA | 7525 |
rs137948751 | in-del | -/CC | | | intron-variant | YES1 | GRCh38.p7 | 18:792554 | TCTCTCTCTCTCTCT[-/CC]CCCTCTGTATATGTG | 7525 |
rs137958686 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | YES1 | GRCh38.p7 | 18:779757 | CTTTTGTCAAGATTT[C/T]TGACCAGCAAATTAC | 7525 |
rs137964979 | snp | A/C | 0.0283406 | 0.115616 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:813170 | TTCTCCTGCTTGTCA[A/C]CTGTGGAAACAGCGA | 7525 |
rs137970170 | snp | A/G | | | intron-variant | YES1 | GRCh38.p7 | 18:739946 | TTTGTGCAGTTTTGC[A/G]GTTTCCAAATAATTA | 7525 |
rs138074397 | in-del | -/A | | | intron-variant | YES1 | GRCh38.p7 | 18:764120 | GCGAGACTCCCTCTC[-/A]AAAAAAAAAAAAAAA | 7525 |
rs138077330 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | YES1 | GRCh38.p7 | 18:809060 | GAGTTTTAATTGTCA[C/T]GTTATGTAATTTTCA | 7525 |
rs138161613 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | YES1 | GRCh38.p7 | 18:766917 | ATTTCTCCCAGTTCA[C/T]AGGTTGCCTTTGCAT | 7525 |
rs138167572 | in-del | -/C | 0.00993419 | 0.0697739 | intron-variant | YES1 | GRCh38.p7 | 18:774863 | TATGGCCTTCAAGAT[-/C]CCAATAACCTATTAT | 7525 |
rs138219628 | in-del | -/C | 0.147991 | 0.228242 | intron-variant | YES1 | GRCh38.p7 | 18:801957 | ATTTTCCATTACAAA[-/C]CCCCAACTTACAAAA | 7525 |
rs138226444 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | YES1 | GRCh38.p7 | 18:796888 | AATAGATTTAATAAC[G/T]AGCAGTAGTGAGGTA | 7525 |
rs138234229 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:775607 | TTTGAGACCACCCTG[A/C]GCAACATAATGAGAC | 7525 |
rs138285439 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:761912 | AACATCATGGCTGGG[C/T]ATCGTGGCTCATGCC | 7525 |
rs138322794 | in-del | -/A | | | intron-variant | YES1 | GRCh38.p7 | 18:732738 | GGGGACTATGAGAAG[-/A]AATAAAGGCCTTTTC | 7525 |
rs138371279 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:799587 | AGGTGGTGCATGCCC[A/G]TAATGAGCAACTCAG | 7525 |
rs138399395 | snp | C/G | | | intron-variant | YES1 | GRCh38.p7 | 18:732167 | TACCATGATGGGCAC[C/G]GTGGCTCACGCCTGT | 7525 |
rs138436447 | snp | A/G | 0.0126979 | 0.078662 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:775712 | TGAGGTTGGAGGATC[A/G]CTTGAGCCTGGGAGA | 7525 |
rs138469185 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | YES1 | GRCh38.p7 | 18:780183 | TTAGCCAAGATCATG[C/T]CACTGCCCTCTGCAC | 7525 |
rs138477921 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:791959 | ACTCGAAATCGGGTG[C/T]GTATTTTACACTTAC | 7525 |
rs138513939 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | YES1 | GRCh38.p7 | 18:743357 | TGCTAGACCTTGAGT[C/T]TGAGGTTTCACAGTT | 7525 |
rs138526506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:754392 | AGGATTGCACATAGG[C/T]GGGTCATTCTCACTT | 7525 |
rs138530238 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | YES1 | GRCh38.p7 | 18:785023 | ACTGTTAGGGTTCAG[A/T]GAGTCAGTATGCTTC | 7525 |
rs138587375 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:795140 | CCCTTTTGGGGAACA[C/T]AACTGAATCCGCAAC | 7525 |
rs138607248 | in-del | -/ATAAACCCGAG | 0.00716266 | 0.059414 | intron-variant | YES1 | GRCh38.p7 | 18:798876 | CCTGCTACTTTTAAT[-/ATAAACCCGAG]ATGACATGACTCCTA | 7525 |
rs138624502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:745128 | TAGTATTAATCATGT[A/G]AAGACTTTCAGGTGC | 7525 |
rs138631207 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | YES1 | GRCh38.p7 | 18:771667 | TATCCTCCCACCTCA[A/G]CCTCTCTAGTAGCTG | 7525 |
rs138740350 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:800943 | ACGAGGTCAGGAGAT[A/C]GAGACCATCCTGGCC | 7525 |
rs138785451 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:739151 | ATTTTCTAAGAAACC[A/G]TATGATACAGGACAC | 7525 |
rs138815289 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | YES1 | GRCh38.p7 | 18:759225 | TAATCCCAACACTTT[A/G]GGAGGCCAAAATGGG | 7525 |
rs138815540 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | YES1 | GRCh38.p7 | 18:804427 | AGCCTGGCCAACATG[A/G]TGAAACCCCCATCTC | 7525 |
rs138850311 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:735347 | AAATAATGTCTTTTG[C/G]AGAAACTTAGAGCTA | 7525 |
rs138854609 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:766089 | AACAGCCATTCTTCC[A/T]CTTCTTTGATAAAAA | 7525 |
rs138900739 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:727395 | AGTATTTGTGTATGT[A/G]TTTAAAATCCAGTCT | 7525 |
rs138902821 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | YES1 | GRCh38.p7 | 18:799155 | AATATTCTAACCACA[C/T]TTGTAGAACCAAGTG | 7525 |
rs138908805 | snp | C/G/T | 0.000181186 | 0.00951642 | synonymous-codon | YES1 | GRCh38.p7 | 18:756621 | TGCACCTCCAAAAGG[C/G/T]GTTACCCCTGAGGAT | 7525 |
rs138936775 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:745189 | TTGAGACAGAAGATT[A/C]TAATATTAAATACCT | 7525 |
rs138975876 | in-del | -/AG | 0.242488 | 0.249887 | intron-variant | YES1 | GRCh38.p7 | 18:732371 | GAACCCGGGAGACAG[-/AG]GTTGCAGTGAGCCAG | 7525 |
rs138983533 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:785059 | TAAGCAACATAACTG[C/T]TAAATTAGGAGGATC | 7525 |
rs139011999 | in-del | -/AC | 0.00993419 | 0.0697739 | intron-variant | YES1 | GRCh38.p7 | 18:785624 | TTAATCCACAATGCA[-/AC]AGTGTTGAGAGGTGG | 7525 |
rs139043930 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:806507 | GATTTGTTTTGTTTG[C/T]GAAAAGTCCATAGCT | 7525 |
rs139095553 | in-del | -/C | | | intron-variant | YES1 | GRCh38.p7 | 18:801958 | TTTTCCATTACAAAC[-/C]CCCAACTTACAAAAA | 7525 |
rs139152764 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | YES1 | GRCh38.p7 | 18:801183 | TAAAAATAAAATAAA[A/G]TTAGCCAGGCATAGT | 7525 |
rs139200126 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:758246 | CTTAAAAATCTGATG[A/T]GTATTTTGTACTTGA | 7525 |
rs139250574 | snp | A/C | | | missense | YES1 | GRCh38.p7 | 18:756615 | GGAAGATGCACCTCC[A/C]AAAGGCGTTACCCCT | 7525 |
rs139289394 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | YES1 | GRCh38.p7 | 18:741398 | TGTGTGTGCAACCAC[A/G]TCCTGCTAATTTTTT | 7525 |
rs139332425 | snp | G/T | | | intron-variant | YES1 | GRCh38.p7 | 18:755175 | GGCTGGAATTAAGAC[G/T]GTAATTGACTTAACA | 7525 |
rs139397085 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:809980 | GTATTCTATGCTTCT[A/G]TTTTTACGTTCACAG | 7525 |
rs139459125 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | YES1 | GRCh38.p7 | 18:759405 | CCAGGAGGCGGAGGT[C/T]GCAGTGAGCCAAGAT | 7525 |
rs139467999 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | YES1 | GRCh38.p7 | 18:768930 | CTGGTCTTGAACTCC[C/T]GACCTCCAGTGATCC | 7525 |
rs139478090 | in-del | -/ACAC | | | intron-variant | YES1 | GRCh38.p7 | 18:795912 | TATCCCAGAACTTAA[-/ACAC]ACACACACACACACA | 7525 |
rs139514518 | in-del | -/CAGATAGGAAGGCATTC | 0.498182 | 0.0300969 | intron-variant | YES1 | GRCh38.p7 | 18:736200 | CAACAACAAACATTA[-/CAGATAGGAAGGCATTC]CAGATGGAGGTAACT | 7525 |
rs139526244 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | YES1 | GRCh38.p7 | 18:767868 | ACAACAACTGGCTAA[C/T]TTTTGTATTTTTAGT | 7525 |
rs139569872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:764579 | AAGGTAGAGGACAGA[A/G]GAAAAGATTTTTTGG | 7525 |
rs139605707 | snp | C/G/T | 0.0138799 | 0.0821421 | intron-variant | YES1 | GRCh38.p7 | 18:764925 | ATTTTTAGTAGAGAC[C/G/T]GGGTTTCACTATGTT | 7525 |
rs139669835 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | YES1 | GRCh38.p7 | 18:729871 | ACCTTGTGATCCACC[C/T]GCCTTGGCTTCCCAA | 7525 |
rs139702973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:773570 | GTGAGGAAAGACAGA[C/T]ACCAAGAAATGCTAC | 7525 |
rs139749137 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:736032 | AAAGAATTAGTCAGG[C/T]GTGGTAGTGTGCACC | 7525 |
rs139749589 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:777680 | GGCATGGTGGTGTGC[A/G]CCTGTAATCCCAGCT | 7525 |
rs139783035 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:776576 | TAATTTTCTGTGTAT[C/T]GGAGGAGTAGGATTT | 7525 |
rs139783259 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | YES1 | GRCh38.p7 | 18:734423 | AATTAGCCGAGCTTG[A/G]TGGCAGGCACCTGTA | 7525 |
rs139822727 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:740920 | TTTATTTATTTGAAA[C/G/T]GGAGTCTCACTCAGT | 7525 |
rs139894149 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | YES1 | GRCh38.p7 | 18:736306 | AGCACCGCTACCATT[C/T]TGGGCCTGATAATTC | 7525 |
rs139915421 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | YES1 | GRCh38.p7 | 18:793661 | CCTTATACAAAAAAA[G/T]TAAGAGAATTAACTG | 7525 |
rs139955149 | snp | C/T | 1.66128e-05 | 0.00288204 | intron-variant | YES1 | GRCh38.p7 | 18:756533 | TTCTCAAACAGACAA[C/T]ATAATTGTCCATTTA | 7525 |
rs139987244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:752190 | TTGGCTTGCTGTAAC[C/T]TCTGCCTCCTAGGTT | 7525 |
rs139988031 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | YES1 | GRCh38.p7 | 18:797633 | GCACTTCTAAACAAC[C/T]GTTAAAAATTACTTC | 7525 |
rs140010323 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:781731 | ACTGTGATCCTTGAT[C/T]AAATTACTTTATCTT | 7525 |
rs140125960 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | YES1 | GRCh38.p7 | 18:810486 | AAGGAATCAATTTTG[C/T]GGTTTATGAAGTCAG | 7525 |
rs140147810 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | YES1 | GRCh38.p7 | 18:779237 | GGAGACCCCCGTCCC[A/G]GCAAAAAATTTTTTA | 7525 |
rs140163437 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:773516 | TGACAGTCATGTTTC[A/G]ATTCAAAATCCTGTA | 7525 |
rs140230854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:794466 | TTTGGATTTTTGTTA[C/T]AAAGAATATTATTAG | 7525 |
rs140308137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:748303 | TCAACCTAAGACAGA[C/T]GATAGTGAATAAAAC | 7525 |
rs140364603 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | YES1 | GRCh38.p7 | 18:805805 | CAATGTGAAGTATTA[A/C]CTTATACACAACCAC | 7525 |
rs140429143 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:801559 | ATCAGGCAATAAAGA[C/G]CTTCCATCTATTTCT | 7525 |
rs140443779 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | YES1 | GRCh38.p7 | 18:808920 | TATTTTATGCTGAGA[C/T]TTCATGGCATTCTTA | 7525 |
rs140451392 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | YES1 | GRCh38.p7 | 18:730485 | AAAGTGCTGGGATTA[C/T]AGGAGTGAGTCACCA | 7525 |
rs140526381 | snp | C/T | 0.000153988 | 0.00877328 | missense | YES1 | GRCh38.p7 | 18:736931 | GGTGAATATAGTTCA[C/T]TCTTTCAATATATGC | 7525 |
rs140585085 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | YES1 | GRCh38.p7 | 18:771275 | GGGAAGCTGAGGCAT[A/G]AGACTCATTTGAACC | 7525 |
rs140628520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:766135 | TGATCCTTCTTACGT[C/T]TGCCAAGTCCTTCAG | 7525 |
rs140639171 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:761205 | TACTGTTCCCCACCC[A/C]ACTTTCTGTCAGGGC | 7525 |
rs140669048 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | YES1 | GRCh38.p7 | 18:731733 | AGCATTCTGGGAGGC[C/T]GAGGCGGGCAGATCA | 7525 |
rs140732624 | snp | C/T | 0.0217537 | 0.101998 | intron-variant | YES1 | GRCh38.p7 | 18:745933 | ATACTTATACTAATA[C/T]AACAATATTCATACC | 7525 |
rs140763056 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722044 | ACTATACAATTGTTA[C/T]TATATAAGGAACTGC | 7525 |
rs140799361 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | YES1 | GRCh38.p7 | 18:750622 | AGCAAGTGACAAATT[G/T]TAATTCAAAATGTGA | 7525 |
rs140865222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:746298 | CTCAAAACTCCACCT[A/G]ACAGTCACAGGAACA | 7525 |
rs140867189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:782498 | AAAATACTTAGGGCT[C/T]ACTACTCCATCTACT | 7525 |
rs140929276 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:771524 | ATCTGTTAAACCACT[C/T]CGTGGCATTTTTCTT | 7525 |
rs140938129 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | YES1 | GRCh38.p7 | 18:784413 | AACTAGTAAGTGACA[G/T]AGCCAGAAGCTGAGA | 7525 |
rs140993283 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | YES1 | GRCh38.p7 | 18:802204 | TAATGAGCTATGATC[A/G]TGCCACTGCACTCCA | 7525 |
rs141001717 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | YES1 | GRCh38.p7 | 18:747519 | ATATGGGATGCATAT[A/C]TATACCAATATACCC | 7525 |
rs141113323 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:726943 | GCTTTGAAATGGACA[A/C]TCTGCTGTAAGAACA | 7525 |
rs141133644 | snp | C/G | 0.0283406 | 0.115616 | intron-variant | YES1 | GRCh38.p7 | 18:760275 | AGGAGTTTGAGACCA[C/G]CCTGGCCAACATGGT | 7525 |
rs141139424 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:773130 | TACACATTTTAGCAA[A/C]ATGCACTGAAAGTAA | 7525 |
rs141218426 | snp | G/T | 0.234692 | 0.249531 | downstream-variant-500B | YES1 | GRCh38.p7 | 18:721373 | AAACCCCGTCTCTAC[G/T]AAAAAATACAAAAAA | 7525 |
rs141274385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:807774 | GTATAGCTAATTCTA[A/G]AAGTTATCCCTCTTG | 7525 |
rs141278786 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:734791 | TATGGAAAACAGTAT[G/T]GAAACTCCTTAAAGA | 7525 |
rs141308273 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:803778 | ATCAGAGCACTTGTA[A/G]GCCAAATATTTTATT | 7525 |
rs141311656 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | YES1 | GRCh38.p7 | 18:731836 | GCTGGGCGTGGTGGC[A/G]GGTGCCTATAGTCCT | 7525 |
rs141371553 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:800989 | CGTCTCTACTAAAAA[C/T]ATAAAAATTAGCTGG | 7525 |
rs141378434 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:729182 | TGTTAATGTGTCTGA[A/C]TCCACTAATCTTGTC | 7525 |
rs141393105 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:775350 | AATGAATTACATAAA[C/G]TCAACACCAATGTAC | 7525 |
rs141442263 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:754572 | AATTAGCCGGGTGCC[A/G]TGGTGTTTGTTTCTT | 7525 |
rs141475886 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:796442 | TTATCATGGTTATAA[A/T]CAACAGCATCAAGCT | 7525 |
rs141530672 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | YES1 | GRCh38.p7 | 18:745144 | AAGACTTTCAGGTGC[A/G]TTCATATGCCAAATT | 7525 |
rs141550462 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:749413 | TGAGGCAGGAGAATC[A/G]CTTGAACCTGGGAGG | 7525 |
rs141621595 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:809756 | TAGACATTACACACT[A/G]GATTCCTTAAAAAAA | 7525 |
rs141795344 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | YES1 | GRCh38.p7 | 18:764233 | TTTCCAGTTTTTTAT[G/T]TTTTTTGAGACTGAG | 7525 |
rs141805950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:794800 | GTGTCTGTCTTCACA[C/T]GTGGGTTTTTGGTTT | 7525 |
rs141808600 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | YES1 | GRCh38.p7 | 18:759284 | CCAGCCTGGCCAACA[C/T]GGTGAAACTCCGTCT | 7525 |
rs141901218 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:758906 | ACAGAAGCACTAATA[C/T]AGAATTCATTAATTC | 7525 |
rs141910747 | in-del | -/CTT | | | intron-variant | YES1 | GRCh38.p7 | 18:727597 | GCTTTTTGTCTTCTC[-/CTT]TTGTTATTTTAGTAG | 7525 |
rs141950792 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | YES1 | GRCh38.p7 | 18:798507 | TTGGAGTGACTGATG[A/G]GGTAGGGTGGGGGAA | 7525 |
rs141971774 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | YES1 | GRCh38.p7 | 18:726528 | GTTCACATCTGTAAT[C/T]CCAGCACTTTGGGAG | 7525 |
rs141978507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:785031 | GGTTCAGAGAGTCAG[C/T]ATGCTTCCATACTAA | 7525 |
rs142007417 | in-del | -/A | 0.252702 | 0.249985 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723103 | CTCAAAAAAGAAAAC[-/A]AAAAAAAAGTGAATG | 7525 |
rs142058366 | in-del | -/C | | | intron-variant | YES1 | GRCh38.p7 | 18:745495 | AAGATATAAGGACCC[-/C]AAATGATGAGAGTCT | 7525 |
rs142075201 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | YES1 | GRCh38.p7 | 18:725396 | TGATATTTAAAATAG[C/T]CTATGATTCTCTAAA | 7525 |
rs142142690 | in-del | -/C | 0.470521 | 0.117772 | intron-variant | YES1 | GRCh38.p7 | 18:732458 | AAAAAAAAAAAAAAA[-/C]AAAACACCAATCACA | 7525 |
rs142154947 | in-del | -/ACTG | | | intron-variant | YES1 | GRCh38.p7 | 18:787075 | AAAACTGTGATACAT[-/ACTG]TCTTTTTTTTTTTTT | 7525 |
rs142167820 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:775633 | GAGACCTCATCTCTA[C/T]AAAAAGTAAAAAAAT | 7525 |
rs142204837 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:776458 | GTGGCACCTTTACAT[A/G]TGTTTACCGGACATT | 7525 |
rs142294402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:788522 | TAGCACATACACGTA[C/T]GGAAGTTTCCACCCA | 7525 |
rs142345780 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | YES1 | GRCh38.p7 | 18:779948 | CTTTAAGAGAGACTA[A/G]AGAGGCTGGGTGCAG | 7525 |
rs142393410 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | YES1 | GRCh38.p7 | 18:741306 | GGGAGTGCAGTGGCA[C/T]AATCACAGCTCACTA | 7525 |
rs142427187 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:781172 | TACTCAGGAGGCTGA[A/G]GCAGAAGAATTGCTT | 7525 |
rs142458568 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | YES1 | GRCh38.p7 | 18:802342 | GGAGGCCAAGGCAGG[A/T]GGATCACCTGAGGTC | 7525 |
rs142534704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:795195 | CTGATGTTGAACTTG[C/T]TGAATTCAGTAACTG | 7525 |
rs142565496 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | YES1 | GRCh38.p7 | 18:798133 | CCCCAGCCAGATAAG[C/T]GTATTGTCTATTTTC | 7525 |
rs142608017 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | YES1 | GRCh38.p7 | 18:757804 | TCCAGCCTGGGTGAC[A/C]GAGTAAGACTCTGTC | 7525 |
rs142616950 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | YES1 | GRCh38.p7 | 18:725659 | TTTGGGAGGCCAAGG[C/T]GGGTGATCATCTGAG | 7525 |
rs142646907 | snp | C/T | 0.000352051 | 0.0132628 | intron-variant | YES1 | GRCh38.p7 | 18:751663 | TGTGTAAAGACCAGA[C/T]TTCTGTCAGTATTTC | 7525 |
rs142660108 | snp | A/C/G | 0.00318978 | 0.0398085 | intron-variant | YES1 | GRCh38.p7 | 18:798704 | TCCCTCCACCAGTGC[A/C/G]CTTCCTAACCTTTCA | 7525 |
rs142687649 | in-del | -/T | 0.159951 | 0.233219 | intron-variant | YES1 | GRCh38.p7 | 18:732432 | CAGAGCAAGACTGTG[-/T]TTTAAAAAAAAAAAA | 7525 |
rs142744369 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | YES1 | GRCh38.p7 | 18:799793 | GTAATCTCAGCTACT[C/T]GGGAGGCTGAGGTGA | 7525 |
rs142752645 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:728086 | CGCACCTGTAATCCC[A/G]GCACTTTGGGAGGAC | 7525 |
rs142763265 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | YES1 | GRCh38.p7 | 18:806088 | TTCACACACATTACT[G/T]CAAGAAAATCAGGAC | 7525 |
rs142802663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:767643 | TCAATGACGATAGTC[A/G]TCATTACTGTAGCTT | 7525 |
rs142865614 | snp | A/T | 0.000164715 | 0.0090736 | synonymous-codon | YES1 | GRCh38.p7 | 18:756636 | CGTTACCCCTGAGGA[A/T]CCTCCAAATGGTGTC | 7525 |
rs142905452 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | YES1 | GRCh38.p7 | 18:807383 | GCACACCTGTGGTCC[A/G]AGCTACTCAGGAGGC | 7525 |
rs142911141 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | YES1 | GRCh38.p7 | 18:771850 | AAAAAATGTTAAAAA[A/G]TATTTCCTTATGTAT | 7525 |
rs142911366 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | YES1 | GRCh38.p7 | 18:776776 | AATCCAACCCAAGGA[A/G]GTTCTAAAATGTTGA | 7525 |
rs142977036 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | YES1 | GRCh38.p7 | 18:765193 | ATACCTCCATAGATA[C/T]GAAAAGATAATCATC | 7525 |
rs142986846 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:751902 | AAAAAAGCTTAAGGA[A/T]AGTTTTTTCTGTAGT | 7525 |
rs143051862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:754341 | ATCTCCTAAATGTTG[C/T]ATTTGTTATTTCCTC | 7525 |
rs143112929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:778947 | GATCTTGCAGGGGTC[A/G]GTAATGGTACCAATT | 7525 |
rs143123744 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:750855 | CATTCCAGAAAAAAG[A/G]AACAGTATGTGTGAA | 7525 |
rs143221049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:774515 | TCGATAAATGTTAAC[A/G]CCATTCTTCTAGTTT | 7525 |
rs143292872 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | YES1 | GRCh38.p7 | 18:734808 | AAACTCCTTAAAGAA[C/T]GAAAAGCAGAACTAC | 7525 |
rs143333869 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:791216 | GATTGTGCCATTGCA[A/C]TCCAGCCTGGCCAAC | 7525 |
rs143342112 | snp | C/T | 0.0174175 | 0.0916809 | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:722820 | AATGTAGGCTGGGCG[C/T]GGTGGCTCACGCCTG | 7525 |
rs143355405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:795266 | ACATACTGAAATATT[C/T]AAGGGTACTGAGACA | 7525 |
rs143356007 | in-del | -/CACA | | | intron-variant | YES1 | GRCh38.p7 | 18:786504 | AGTCCATACACACAC[-/CACA]ACACACACACACACA | 7525 |
rs143359246 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | YES1 | GRCh38.p7 | 18:797986 | TCTTAGGACAAAAAA[C/T]GACAGGGGAAAGCAC | 7525 |
rs143361346 | snp | A/C/T | 0.00636936 | 0.0560724 | intron-variant | YES1 | GRCh38.p7 | 18:752857 | TTGAGACAGGAGAAT[A/C/T]GCTTGAAACCCGGAA | 7525 |
rs143366888 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | YES1 | GRCh38.p7 | 18:725217 | CAGTTCACCCCATCT[C/T]ATCACAGGACAGCAA | 7525 |
rs143427877 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:748749 | CTGACAAATGCTTTT[A/C]TCTTTATAGTACATA | 7525 |
rs143431006 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | YES1 | GRCh38.p7 | 18:793665 | ATACAAAAAAAGTAA[A/G]AGAATTAACTGAAAA | 7525 |
rs143460489 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | YES1 | GRCh38.p7 | 18:791111 | AAAAATTAGCCGGGC[A/G]TGGTGGTGCGCGTTT | 7525 |
rs143469805 | snp | A/G | 0.252983 | 0.249982 | downstream-variant-500B | YES1 | GRCh38.p7 | 18:721311 | GGGAGGCCGAAGCGG[A/G]CGGATCACGAGGTCA | 7525 |
rs143475785 | snp | C/T | 0.000230635 | 0.0107361 | synonymous-codon | YES1 | GRCh38.p7 | 18:747946 | AATGGAATCTGCAGG[C/T]GCTACATAATTGCTC | 7525 |
rs143482769 | snp | A/T | | | intron-variant | YES1 | GRCh38.p7 | 18:772752 | CTCTATTTCTGTATT[A/T]CTGATGTTTCTGGCT | 7525 |
rs143507500 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | YES1 | GRCh38.p7 | 18:756952 | GCAAAAAGGAACATA[A/G]ACAAAACAAAAAATA | 7525 |
rs143551576 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | YES1 | GRCh38.p7 | 18:768084 | TTTTAAGCTTTGTGG[A/G]CCATATGGTGTCTGT | 7525 |
rs143597230 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | YES1 | GRCh38.p7 | 18:804512 | TACTGAGGAGGCTGA[A/G]GCAGGGAGAATTGCT | 7525 |
rs143612519 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | YES1 | GRCh38.p7 | 18:742332 | TCCATTGAAGGTAGT[C/G]GGGAGGCCAGGCACA | 7525 |
rs143626556 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | YES1 | GRCh38.p7 | 18:733145 | TTCATATTGAAATAA[A/G]TCACATTTCTTCCTG | 7525 |
rs143695349 | in-del | -/TGTGTGTG | 0.479106 | 0.100052 | intron-variant | YES1 | GRCh38.p7 | 18:792566 | CTCTCCCTCTGTATA[-/TGTGTGTG]TGTGTGTGTGTGTAT | 7525 |
rs143705522 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | YES1 | GRCh38.p7 | 18:799487 | GGCCAAGGTGGGTGG[A/C]TCACTTGAGGTCAGG | 7525 |
rs143780656 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | YES1 | GRCh38.p7 | 18:758385 | TGGAAACACCCCTAA[C/T]GCTCACCAAATTTAA | 7525 |
rs143782272 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | YES1 | GRCh38.p7 | 18:769273 | ATCTGTATACAAAGT[A/G]TATTTGTATATTACG | 7525 |
rs143847438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:810641 | AAAGGCAATTGTCTT[C/T]TTCAAATGTAGGACC | 7525 |
rs143849463 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | YES1 | GRCh38.p7 | 18:814125 | GTTTGCTTCTCTTCG[C/T]CCTCCCTTTTTTTTT | 7525 |
rs143891710 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:791980 | TTACACTTACAGTAC[A/T]TCTCAATTTGGACTA | 7525 |
rs143922915 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:773533 | TTCAAAATCCTGTAC[A/G]AATTAAAAGGCTGGT | 7525 |
rs143925103 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | YES1 | GRCh38.p7 | 18:787389 | AGGCATGAGCCACCG[C/T]GCCCAGCTGATACAT | 7525 |
rs143947065 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | YES1 | GRCh38.p7 | 18:772969 | GCACTAACCTGCTGA[A/C]CAGTTATGGTTTGGC | 7525 |
rs143949484 | snp | A/C/T | 0.00199481 | 0.0315187 | intron-variant | YES1 | GRCh38.p7 | 18:801347 | CAAAAAAATGATTTA[A/C/T]ATGAACAAACTAGTA | 7525 |
rs143977576 | snp | G/T | | | missense | YES1 | GRCh38.p7 | 18:756723 | TGACACTGTAGTGGG[G/T]TCTGCTCCATAATGG | 7525 |
rs144072971 | snp | C/G/T | 0.00993419 | 0.0697739 | intron-variant | YES1 | GRCh38.p7 | 18:759714 | ATTTATTTCTTTTTT[C/G/T]CTTTTATTATTATTA | 7525 |
rs144087865 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:789161 | TGATAACAGAACATA[C/T]GCTATAAAACCTAAG | 7525 |
rs144131302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:754444 | GGGTGCGGTGGCTCA[C/T]GCATGTAATCCCAGC | 7525 |
rs144160838 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | YES1 | GRCh38.p7 | 18:793328 | ACAGGCGTGAGCCAC[C/T]GCGCCTGGCCATTAT | 7525 |
rs144182385 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YES1 | GRCh38.p7 | 18:801682 | GATTTGAGTACAAAC[C/T]ACATATATATGTATA | 7525 |
rs144246538 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | YES1 | GRCh38.p7 | 18:726687 | TCGGGAGGCTGAGGC[A/G]GGAGAATCACTTGAA | 7525 |
rs144250696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:798552 | AGAAGATGCATAGGG[A/G]AGCCGCTTTAGCTCC | 7525 |
rs144315004 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | YES1 | GRCh38.p7 | 18:780603 | TCTTTATAAATTAGC[C/T]AGTTTCAAGTATTCT | 7525 |
rs144347874 | in-del | -/TCT | | | intron-variant | YES1 | GRCh38.p7 | 18:727595 | TGGCTTTTTGTCTTC[-/TCT]TCTTGTTATTTTAGT | 7525 |
rs144513898 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | YES1 | GRCh38.p7 | 18:810045 | CCCAAGTTTGGGTGA[C/T]CCCAGCGCTTAGCAT | 7525 |
rs144522048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:736137 | GAAATCACGCCACTA[C/T]ACTCTAGCCTGAGCA | 7525 |
rs144556747 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | YES1 | GRCh38.p7 | 18:798080 | AAGTGCAATGGATGA[A/G]CCTCACTCTGAGAAC | 7525 |
rs144575859 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | YES1 | GRCh38.p7 | 18:784798 | TATTATGCCTACCTG[G/T]ATAAGCCAGGATAAA | 7525 |
rs144591033 | snp | G/T | 0.000153988 | 0.00877328 | missense | YES1 | GRCh38.p7 | 18:742993 | GAACAAGTTTATCAT[G/T]TCTTAATTTTTTCAT | 7525 |
rs144595828 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | YES1 | GRCh38.p7 | 18:746532 | TGACAGTGTCTGCTA[C/T]GGAAGAGCTCACAGA | 7525 |
rs144662277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:750939 | TATGTCTGGGTATTA[A/G]AGTTAGAAGAGGGGA | 7525 |
rs144675316 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | YES1 | GRCh38.p7 | 18:744940 | AATGAGACATGTTCT[C/T]TCCTATTCTCACTAA | 7525 |
rs144771301 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | YES1 | GRCh38.p7 | 18:745601 | TTATTGGGCATGTAT[C/T]ATGTGTAAATAAGTG | 7525 |
rs144830903 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:747524 | GGATGCATATATATA[C/T]CAATATACCCATCCC | 7525 |
rs144872080 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:754200 | ATAAAACCTAAACTC[A/G]CTACCAGAGTCTGTG | 7525 |
rs144961975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:804045 | TGTTTTAGAAAATCT[A/G]TTTTACAAACCTTAA | 7525 |
rs144974891 | snp | C/T | | | intron-variant | YES1 | GRCh38.p7 | 18:747416 | AGAGGTTGCAGTGAG[C/T]CGAGATCACGCCACT | 7525 |
rs145012992 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | YES1 | GRCh38.p7 | 18:764941 | GGGTTTCACTATGTT[A/G]GCCAGACTAGTCTCA | 7525 |
rs145037346 | in-del | -/AT | | | utr-variant-3-prime | YES1 | GRCh38.p7 | 18:723395 | TGTAAAACTTTCACT[-/AT]TTCTTTTCTCGTATT | 7525 |
rs145041362 | in-del | -/TAAC | | | intron-variant | YES1 | GRCh38.p7 | 18:746941 | ACATGTATTTTTTCT[-/TAAC]TAATTGTAAGTTGCA | 7525 |
rs145059757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:763838 | CATTAAGAAAAAGTC[A/G]AGGCCAGGCGCAGTG | 7525 |
rs145060781 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | YES1 | GRCh38.p7 | 18:807796 | TCCCTCTTGAAGGCC[G/T]TCCACTTCCTAGGAG | 7525 |
rs145090996 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | YES1 | GRCh38.p7 | 18:730301 | CTCCCAGAGACTCTC[C/T]CTGTGTATGTGCAGA | 7525 |
rs145134519 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | YES1 | GRCh38.p7 | 18:765893 | TCATGAAGACAAAAG[C/T]GAGATTGCAGTAAGT | 7525 |
rs145256073 | in-del | -/GCGGCGGCG | 0.311884 | 0.24222 | intron-variant | YES1 | GRCh38.p7 | 18:812017 | CGGGGGCGGGGAACC[-/GCGGCGGCG]GCGGCGGCGGCGGCT | 7525 |
rs145342028 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | YES1 | GRCh38.p7 | 18:782064 | CCATCACTTCCCTTG[C/T]TTCCCCATTTTCTCT | 7525 |
rs145394087 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:777993 | GTTACACTGTTAAAG[A/T]ATTTTGCTTTAATAC | 7525 |
rs145406545 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | YES1 | GRCh38.p7 | 18:769070 | CATTCAGTATAGTGA[A/C]ATGTTTGTAGCCTAG | 7525 |
rs145471220 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YES1 | GRCh38.p7 | 18:741673 | CTATGTGTGGTGGCA[C/T]GCACCTGTAATCCCA | 7525 |
rs145478539 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | YES1 | GRCh38.p7 | 18:730836 | ACATTTAAAGTGACA[A/C]TATGTTGCATGGCTG | 7525 |
rs145500860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YES1 | GRCh38.p7 | 18:784368 | AACTAAGGCTGGAGA[C/T]GTTAAATAGGTTTTG | 7525 |