| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs34377097 | 1.000 | 19 | 3600456 | missense variant | C/A | snv | 5.8E-05 | 2.1E-05 | 2 | ||
| rs387906691 | 1.000 | 19 | 3595810 | missense variant | C/T | snv | 2 | ||||
| rs757075712 | 0.763 | 0.200 | 10 | 58390856 | missense variant | C/T | snv | 1.6E-05 | 1.4E-05 | 15 | |
| rs72547528 | 0.925 | 0.120 | 16 | 31091334 | missense variant | G/A;C | snv | 7.2E-05; 8.1E-06 | 3 | ||
| rs61749397 | 0.807 | 0.080 | 12 | 6019472 | missense variant | C/G;T | snv | 4.0E-06 | 9 | ||
| rs61750610 | 0.925 | 0.080 | 12 | 6013630 | missense variant | G/T | snv | 3 |