| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121913530 | 0.583 | 0.640 | 12 | 25245351 | missense variant | C/A;G;T | snv | 63 | |||
| rs121913254 | 0.658 | 0.440 | 1 | 114713909 | stop gained | G/A;C;T | snv | 31 | |||
| rs121913250 | 0.683 | 0.440 | 1 | 114716127 | missense variant | C/A;G;T | snv | 25 | |||
| rs121913238 | 0.732 | 0.240 | 12 | 25227343 | missense variant | G/C;T | snv | 17 | |||
| rs63751428 | 0.882 | 0.160 | 3 | 36996686 | stop gained | C/A;T | snv | 5 | |||
| rs876660952 | 1.000 | 0.040 | 3 | 37028854 | missense variant | T/G | snv | 4.0E-06 | 1 |