| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121913500 | 0.529 | 0.600 | 2 | 208248388 | missense variant | C/A;G;T | snv | 4.0E-06 | 96 | ||
| rs121913499 | 0.605 | 0.520 | 2 | 208248389 | missense variant | G/A;C;T | snv | 51 | |||
| rs118101777 | 0.614 | 0.280 | 15 | 90087472 | missense variant | C/T | snv | 2.0E-03 | 1.6E-03 | 42 | |
| rs1057519736 | 0.752 | 0.160 | 15 | 90088605 | missense variant | C/G | snv | 13 | |||
| rs137854532 | 0.882 | 0.160 | 20 | 58905443 | missense variant | C/T | snv | 4 | |||
| rs121434601 | 0.925 | 0.080 | 3 | 46898097 | missense variant | C/T | snv | 1.7E-03 | 1.7E-03 | 3 | |
| rs1369025856 | 0.925 | 0.080 | 20 | 58910061 | missense variant | G/A | snv | 2 | |||
| rs1203182324 | 1.000 | 0.040 | 20 | 58854258 | missense variant | G/A | snv | 1 | |||
| rs1328937750 | 1.000 | 0.040 | 20 | 58853674 | missense variant | G/A | snv | 1 | |||
| rs375486178 | 1.000 | 0.040 | 20 | 58853828 | missense variant | G/A | snv | 4.6E-06 | 1.4E-05 | 1 | |
| rs1131691907 | 1.000 | 0.040 | 20 | 58840473 | missense variant | A/G | snv | 1 | |||
| rs1027263198 | 1.000 | 0.040 | 3 | 46898787 | missense variant | G/A | snv | 8.7E-06 | 1.4E-05 | 1 | |
| rs200197785 | 1.000 | 0.040 | 3 | 46897905 | missense variant | G/A | snv | 2.0E-05 | 1.4E-05 | 1 |