| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121913495 | 0.672 | 0.400 | 20 | 58909366 | missense variant | G/A;T | snv | 28 | |||
| rs11554273 | 0.689 | 0.240 | 20 | 58909365 | missense variant | C/A;G;T | snv | 4.0E-06 | 22 | ||
| rs121913494 | 0.827 | 0.240 | 20 | 58909541 | missense variant | A/G;T | snv | 7 | |||
| rs1440530084 | 0.882 | 0.040 | 17 | 42563227 | missense variant | G/A | snv | 4.0E-06 | 1.4E-05 | 3 | |
| rs761347168 | 1.000 | 17 | 42563226 | missense variant | C/T | snv | 8.0E-06 | 1 |