| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs587780564 | 0.882 | 0.080 | 14 | 101986017 | missense variant | C/T | snv | 5 | |||
| rs121913598 | 0.851 | 0.080 | 1 | 161307361 | missense variant | G/A | snv | 5 | |||
| rs371856018 | 0.882 | 0.120 | 1 | 161307376 | missense variant | T/C;G | snv | 8.0E-06 | 5 | ||
| rs119483085 | 0.851 | 0.160 | 8 | 133258374 | stop gained | G/A | snv | 7.0E-06 | 5 | ||
| rs207482230 | 0.882 | 0.080 | 3 | 100748182 | missense variant | C/T | snv | 4.0E-06 | 5 | ||
| rs80338934 | 0.882 | 0.080 | 5 | 149010272 | stop gained | G/A | snv | 4.0E-05 | 3.5E-05 | 4 | |
| rs587777425 | 1.000 | 1 | 160237145 | missense variant | G/A;T | snv | 3 | ||||
| rs121913584 | 0.925 | 0.080 | 1 | 161306886 | missense variant | G/A;C;T | snv | 3.2E-05 | 3 | ||
| rs200092345 | 8 | 19458576 | missense variant | T/C | snv | 1.2E-05 | 1.4E-05 | 2 | |||
| rs533235539 | 8 | 19405853 | missense variant | A/C | snv | 1.5E-04 | 9.8E-05 | 2 | |||
| rs1334828551 | 1 | 20500800 | missense variant | A/G | snv | 4.0E-06 | 1.4E-05 | 2 |