| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs113488022 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 490 | ||
| rs121913529 | 0.492 | 0.680 | 12 | 25245350 | missense variant | C/A;G;T | snv | 4.0E-06 | 144 | ||
| rs11545664 | 0.925 | 0.120 | 9 | 127843106 | synonymous variant | C/T | snv | 9.3E-02 | 0.14 | 4 | |
| rs201393380 | 0.925 | 0.120 | 9 | 127825767 | missense variant | C/G | snv | 1.3E-04 | 7.8E-04 | 4 |