| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1475145065 | 0.882 | 0.080 | 14 | 24574706 | missense variant | C/G;T | snv | 4.0E-06; 8.0E-06 | 3 | ||
| rs773829498 | 0.882 | 0.080 | 7 | 101130457 | missense variant | A/G | snv | 4.0E-06 | 3 | ||
| rs34758144 | 1.000 | 0.080 | 21 | 43058472 | intron variant | G/A;T | snv | 1 | |||
| rs3917615 | 1.000 | 0.080 | 1 | 94536434 | intron variant | C/A;T | snv | 1 |