| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs188709583 | 1.000 | 16 | 20337383 | missense variant | C/A;T | snv | 4.0E-06; 1.3E-04 | 3 | |||
| rs121917769 | 0.925 | 0.240 | 16 | 20348925 | missense variant | A/G | snv | 2 | |||
| rs768597701 | 1.000 | 16 | 20349795 | missense variant | C/T | snv | 5.4E-05 | 1 |