| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1799971 | 0.559 | 0.600 | 6 | 154039662 | missense variant | A/G | snv | 0.19 | 0.12 | 95 | |
| rs199953844 | 6 | 154039650 | missense variant | C/A;T | snv | 4.0E-06; 1.2E-04 | 2 | ||||
| rs13438494 | 1.000 | 0.040 | 7 | 82759398 | intron variant | T/G | snv | 0.61 | 6 | ||
| rs1047383 | 20 | 8884359 | 3 prime UTR variant | C/T | snv | 0.56 | 1 | ||||
| rs25531 | 0.581 | 0.520 | 17 | 30237328 | upstream gene variant | T/C | snv | 0.18 | 72 | ||
| rs750891770 | 1 | 31583538 | missense variant | G/A | snv | 2.8E-05 | 2.1E-05 | 1 |