| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1047891 | 0.827 | 0.200 | 2 | 210675783 | missense variant | C/A | snv | 0.30 | 0.33 | 8 | |
| rs4665972 | 2 | 27375230 | intron variant | T/C | snv | 0.69 | 3 | ||||
| rs702634 | 1.000 | 0.080 | 5 | 53975590 | intron variant | G/A | snv | 0.72 | 1 | ||
| rs1801239 | 0.827 | 0.160 | 10 | 16877053 | missense variant | T/C;G | snv | 8.9E-02; 8.0E-06 | 1 |