| 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 | 116 | |
| rs198851 | 6 | 26104404 | downstream gene variant | T/A;C;G | snv | 15 | |||||
| rs62435145 | 1.000 | 0.040 | 7 | 1246931 | regulatory region variant | G/T | snv | 0.51 | 8 | ||
| rs760077 | 0.925 | 0.120 | 1 | 155208991 | missense variant | T/A | snv | 0.36 | 8 | ||
| rs10480300 | 0.925 | 0.120 | 7 | 151708919 | intron variant | C/T | snv | 0.24 | 6 | ||
| rs11072567 | 15 | 76006403 | intron variant | A/G | snv | 0.43 | 5 | ||||
| rs73728279 | 1.000 | 0.080 | 7 | 151714408 | intron variant | G/A;T | snv | 4 |