Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1015164 | 0.925 | 3 | 46410189 | intron variant | A/C;G;T | snv | 8 | ||||
rs10808739 | 0.882 | 8 | 64727703 | intron variant | G/A | snv | 0.24 | 6 | |||
rs10892324 | 0.925 | 11 | 119032329 | upstream gene variant | T/A;G | snv | 5 | ||||
rs11231017 | 0.925 | 11 | 62293877 | downstream gene variant | G/A | snv | 0.29 | 5 | |||
rs11649112 | 0.925 | 16 | 13267554 | intron variant | G/A | snv | 0.22 | 5 | |||
rs12460243 | 0.925 | 19 | 8066356 | intron variant | G/A | snv | 0.14 | 5 | |||
rs13064773 | 0.925 | 3 | 158893105 | intergenic variant | G/A | snv | 0.39 | 5 | |||
rs16823858 | 0.925 | 3 | 115559835 | intron variant | G/A;C | snv | 5 | ||||
rs16933829 | 0.925 | 11 | 17094129 | intron variant | T/C | snv | 6.2E-02 | 5 | |||
rs17038463 | 0.925 | 3 | 1383484 | intron variant | T/C;G | snv | 5 | ||||
rs17151904 | 0.925 | 7 | 25568789 | TF binding site variant | G/A;C | snv | 5 | ||||
rs17169 | 0.925 | 2 | 8037334 | intron variant | G/T | snv | 0.13 | 5 | |||
rs17691394 | 0.925 | 7 | 126684537 | intron variant | A/G | snv | 0.13 | 5 | |||
rs30388 | 0.925 | 16 | 79580219 | regulatory region variant | T/C;G | snv | 5 | ||||
rs3869068 | 0.925 | 6 | 30036275 | intron variant | C/T | snv | 0.17 | 5 | |||
rs4835796 | 0.925 | 5 | 138446426 | 3 prime UTR variant | T/G | snv | 0.56 | 5 | |||
rs59440261 | 0.925 | 6 | 31403294 | intron variant | C/A | snv | 3.3E-02 | 5 | |||
rs608114 | 0.925 | 6 | 95928822 | intron variant | A/T | snv | 0.95 | 5 | |||
rs61550741 | 0.925 | 21 | 31133966 | intron variant | A/G | snv | 0.12 | 5 | |||
rs6542826 | 0.925 | 2 | 109433263 | intron variant | A/G | snv | 0.51 | 5 | |||
rs6594357 | 0.925 | 5 | 109205522 | intergenic variant | T/A;C | snv | 5 | ||||
rs6723162 | 0.925 | 2 | 70875156 | intergenic variant | A/T | snv | 0.65 | 5 | |||
rs7458938 | 0.925 | 7 | 125820594 | intergenic variant | G/A | snv | 0.72 | 5 | |||
rs7576600 | 0.925 | 2 | 40840846 | intergenic variant | C/A;G | snv | 5 | ||||
rs183662584 | 1.000 | 3 | 46373218 | missense variant | G/A | snv | 5.2E-04 | 1.5E-04 | 2 |