| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121913529 | 0.492 | 0.680 | 12 | 25245350 | missense variant | C/A;G;T | snv | 4.0E-06 | 144 | ||
| rs1137282 | 0.851 | 0.120 | 12 | 25209843 | missense variant | A/G;T | snv | 0.19 | 5 | ||
| rs9513070 | 0.851 | 0.080 | 13 | 28305702 | intron variant | G/A | snv | 0.54 | 4 |