| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10737680 | 0.827 | 0.080 | 1 | 196710325 | intron variant | A/C | snv | 0.44 | 9 | ||
| rs2869966 | 1.000 | 0.040 | 4 | 88947927 | intron variant | C/T | snv | 0.47 | 9 | ||
| rs117068593 | 14 | 92651884 | missense variant | C/T | snv | 0.13 | 0.11 | 4 | |||
| rs13116999 | 4 | 144521212 | intron variant | G/A | snv | 0.65 | 4 | ||||
| rs8042849 | 1.000 | 0.040 | 15 | 78525587 | intron variant | C/T | snv | 0.65 | 4 | ||
| rs11621587 | 14 | 92631994 | intron variant | G/C;T | snv | 3 |