Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1013443 | 5 | 180774114 | intergenic variant | A/T | snv | 1.4E-03 | 1 | ||||
rs10958725 | 8 | 42669441 | intergenic variant | T/G | snv | 0.63 | 1 | ||||
rs10958726 | 8 | 42680766 | intergenic variant | G/T | snv | 0.66 | 1 | ||||
rs11071927 | 15 | 66968834 | intergenic variant | C/A | snv | 0.85 | 1 | ||||
rs11205277 | 1.000 | 0.120 | 1 | 149920979 | upstream gene variant | A/C;G;T | snv | 1 | |||
rs12461383 | 19 | 40864433 | intron variant | C/G | snv | 0.42 | 1 | ||||
rs13273442 | 0.882 | 0.080 | 8 | 42688874 | intergenic variant | A/G | snv | 0.66 | 1 | ||
rs1383634 | 15 | 78737054 | downstream gene variant | T/C | snv | 0.53 | 1 | ||||
rs1443512 | 12 | 53948900 | downstream gene variant | A/C;T | snv | 1 | |||||
rs1451239 | 8 | 42691399 | intergenic variant | G/A;T | snv | 1 | |||||
rs1496402 | 19 | 40860229 | intron variant | T/A | snv | 0.67 | 1 | ||||
rs1678618 | 10 | 72046530 | intergenic variant | A/G | snv | 0.39 | 1 | ||||
rs1776897 | 6 | 34227234 | regulatory region variant | G/T | snv | 0.80 | 1 | ||||
rs1979140 | 8 | 42675693 | intergenic variant | T/C | snv | 0.63 | 1 | ||||
rs2219939 | 1.000 | 0.040 | 15 | 78737381 | downstream gene variant | G/A | snv | 0.53 | 1 | ||
rs2568500 | 15 | 78434586 | upstream gene variant | C/T | snv | 0.46 | 1 | ||||
rs2869030 | 15 | 78419461 | regulatory region variant | G/T | snv | 0.66 | 1 | ||||
rs2869032 | 15 | 78422219 | regulatory region variant | C/G;T | snv | 1 | |||||
rs2869045 | 15 | 78426557 | regulatory region variant | T/C | snv | 0.78 | 1 | ||||
rs3025343 | 9 | 133613233 | non coding transcript exon variant | G/A | snv | 7.0E-02 | 1 | ||||
rs34325700 | 8 | 42673524 | intergenic variant | -/A | delins | 1 | |||||
rs4105144 | 0.827 | 0.160 | 19 | 40852719 | intron variant | T/C | snv | 1 | |||
rs4275821 | 15 | 78557199 | downstream gene variant | C/T | snv | 0.69 | 1 | ||||
rs4343391 | 19 | 40838463 | intron variant | G/C | snv | 0.72 | 1 | ||||
rs4362358 | 15 | 78503762 | upstream gene variant | C/T | snv | 0.50 | 1 |