Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10175798 | 1.000 | 0.120 | 2 | 30226728 | upstream gene variant | G/A | snv | 0.51 | 1 | ||
rs1034323 | 1.000 | 0.120 | 6 | 30400858 | intergenic variant | C/T | snv | 0.43 | 1 | ||
rs1076832 | 1.000 | 0.120 | 6 | 30452054 | non coding transcript exon variant | C/A | snv | 0.15 | 1 | ||
rs10790268 | 1.000 | 0.120 | 11 | 118858682 | intergenic variant | A/G;T | snv | 1 | |||
rs10795791 | 0.925 | 0.200 | 10 | 6066377 | upstream gene variant | A/G | snv | 0.40 | 1 | ||
rs10946213 | 1.000 | 0.120 | 6 | 167102607 | intron variant | C/T | snv | 0.35 | 1 | ||
rs11051970 | 1.000 | 0.120 | 12 | 32384554 | downstream gene variant | G/T | snv | 0.33 | 1 | ||
rs11148643 | 1.000 | 0.120 | 13 | 64317065 | intergenic variant | T/A;C | snv | 0.46 | 1 | ||
rs113652681 | 1.000 | 0.120 | 6 | 33339623 | downstream gene variant | -/G;TG | ins | 1 | |||
rs11571302 | 0.925 | 0.200 | 2 | 203878211 | downstream gene variant | G/A;T | snv | 1 | |||
rs1158785 | 1.000 | 0.120 | 6 | 32790794 | intergenic variant | T/A;C | snv | 1 | |||
rs11752073 | 1.000 | 0.120 | 6 | 28237015 | downstream gene variant | G/T | snv | 0.13 | 1 | ||
rs11761231 | 1.000 | 0.120 | 7 | 131685280 | intergenic variant | T/C | snv | 0.66 | 1 | ||
rs11900673 | 1.000 | 0.120 | 2 | 62225526 | downstream gene variant | C/T | snv | 0.13 | 1 | ||
rs11902322 | 1.000 | 0.120 | 2 | 207050753 | intergenic variant | A/G | snv | 0.33 | 1 | ||
rs11933540 | 1.000 | 0.120 | 4 | 26118379 | downstream gene variant | T/C | snv | 0.37 | 1 | ||
rs11966319 | 1.000 | 0.120 | 6 | 31261901 | intergenic variant | C/A;G;T | snv | 1 | |||
rs11966332 | 1.000 | 0.120 | 6 | 31261924 | intergenic variant | C/T | snv | 0.14 | 1 | ||
rs12109285 | 1.000 | 0.120 | 5 | 21749239 | intron variant | T/A;C | snv | 1 | |||
rs12191360 | 1.000 | 0.120 | 6 | 32483584 | intergenic variant | C/A;T | snv | 1 | |||
rs1219414 | 1.000 | 0.120 | 11 | 121927189 | intron variant | G/A | snv | 0.31 | 1 | ||
rs1233665 | 1.000 | 0.120 | 6 | 28210734 | intergenic variant | T/A;C | snv | 1 | |||
rs12413578 | 0.882 | 0.160 | 10 | 9007290 | intergenic variant | C/G;T | snv | 1 | |||
rs12524487 | 0.925 | 0.160 | 6 | 31386461 | upstream gene variant | C/T | snv | 5.9E-02 | 1 | ||
rs12525220 | 1.000 | 0.120 | 6 | 32707693 | upstream gene variant | G/A | snv | 5.6E-02 | 1 |