| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs75076352 | 0.689 | 0.240 | 10 | 43114500 | missense variant | T/A;C;G | snv | 1.2E-05 | 24 | ||
| rs75996173 | 0.716 | 0.240 | 10 | 43114501 | missense variant | G/A;C;T | snv | 4.0E-06; 4.0E-06 | 21 | ||
| rs104893717 | 0.925 | 0.040 | 3 | 122254227 | missense variant | T/C | snv | 3 | |||
| rs200673016 | 0.925 | 0.040 | 3 | 122254221 | missense variant | T/C | snv | 4.2E-05 | 3 |