| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs13107325 | 0.776 | 0.520 | 4 | 102267552 | missense variant | C/A;T | snv | 4.0E-06; 4.5E-02 | 24 | ||
| rs2277339 | 12 | 56752285 | missense variant | T/G | snv | 0.12 | 0.14 | 10 | |||
| rs13389219 | 1.000 | 0.080 | 2 | 164672366 | intron variant | C/T | snv | 0.47 | 5 | ||
| rs10761785 | 10 | 63559006 | intron variant | G/T | snv | 0.51 | 3 | ||||
| rs62621409 | 11 | 36437447 | missense variant | A/G | snv | 3.9E-02 | 3.5E-02 | 3 | |||
| rs62271373 | 3 | 150348753 | regulatory region variant | T/A | snv | 3.8E-02 | 2 |