| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs564250 | 1.000 | 0.080 | 11 | 34437314 | upstream gene variant | T/A;C | snv | 1 | |||
| rs7602171 | 1.000 | 0.080 | 2 | 169023668 | intron variant | A/G | snv | 0.72 | 1 | ||
| rs775174909 | 1.000 | 0.080 | 19 | 43546720 | missense variant | T/C | snv | 4.1E-06 | 1 | ||
| rs886054499 | 1.000 | 0.080 | 19 | 45364860 | missense variant | G/A | snv | 1 |