| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs671 | 0.529 | 0.840 | 12 | 111803962 | missense variant | G/A | snv | 1.9E-02 | 5.8E-03 | 10 | |
| rs4646776 | 0.925 | 0.120 | 12 | 111792215 | intron variant | G/A;C | snv | 1.9E-02 | 5.8E-03 | 2 | |
| rs2238151 | 1.000 | 0.040 | 12 | 111774029 | intron variant | T/C | snv | 0.52 | 1 | ||
| rs11066028 | 1.000 | 0.080 | 12 | 111807366 | intron variant | A/C | snv | 0.45 | 1 | ||
| rs4648328 | 12 | 111784984 | intron variant | C/T | snv | 0.18 | 1 |