Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs59962885 | 0.807 | 0.200 | 2 | 219420939 | missense variant | G/A;C;T | snv | 6.8E-05 | 11 | ||
rs121913002 | 0.851 | 0.160 | 2 | 219425727 | missense variant | C/A;G;T | snv | 6.5E-05; 5.6E-04 | 7 | ||
rs121913003 | 0.882 | 0.200 | 2 | 219421532 | missense variant | C/T | snv | 6 | |||
rs61368398 | 1.000 | 0.160 | 2 | 219421380 | missense variant | G/A;C;T | snv | 3.2E-05 | 2 |