Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1799971 | 0.559 | 0.600 | 6 | 154039662 | missense variant | A/G | snv | 0.19 | 0.12 | 95 | |
rs62638690 | 0.925 | 0.080 | 6 | 154090110 | missense variant | G/T | snv | 5.6E-03 | 5.6E-03 | 2 | |
rs17174794 | 1.000 | 6 | 154089975 | missense variant | C/G;T | snv | 4.1E-03 | 1 | |||
rs17174801 | 1.000 | 6 | 154089989 | missense variant | A/G | snv | 6.9E-04 | 2.8E-03 | 1 |