| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs71636784 | 1.000 | 0.040 | 1 | 26842709 | intron variant | T/G | snv | 0.12 | 4 | ||
| rs11771259 | 1.000 | 0.040 | 7 | 7237584 | intron variant | C/G | snv | 1.0E-01 | 3 | ||
| rs12627514 | 1.000 | 0.040 | 21 | 43339560 | intergenic variant | C/A;G;T | snv | 3 |