| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs760549861 | 1.000 | 1 | 94014685 | missense variant | G/A | snv | 7.6E-05 | 7.0E-06 | 1 | ||
| rs139250920 | 1.000 | 0.080 | 1 | 94055212 | missense variant | G/A | snv | 1.7E-04 | 2.8E-04 | 1 | |
| rs886044720 | 0.925 | 0.080 | 1 | 94112973 | missense variant | A/C | snv | 1 | |||
| rs61750130 | 0.807 | 0.080 | 1 | 94031110 | missense variant | G/A | snv | 2.4E-04 | 2.3E-04 | 1 | |
| rs1800552 | 0.851 | 0.080 | 1 | 94010821 | missense variant | C/T | snv | 1.6E-03 | 1.5E-03 | 1 | |
| rs61753038 | 0.851 | 0.080 | 1 | 94005470 | stop gained | G/A | snv | 1.2E-05 | 7.0E-06 | 1 | |
| rs61751402 | 0.882 | 0.080 | 1 | 94029515 | missense variant | C/T | snv | 6.3E-05 | 5.6E-05 | 1 | |
| rs61753029 | 1.000 | 1 | 94014590 | missense variant | T/C | snv | 3.2E-05 | 1 | |||
| rs1801269 | 0.851 | 0.080 | 1 | 94041345 | missense variant | C/A;T | snv | 3.1E-04; 4.0E-06 | 1 | ||
| rs781716640 | 1.000 | 1 | 94080709 | missense variant | G/A | snv | 2.0E-05 | 1.4E-05 | 1 | ||
| rs61750654 | 0.925 | 0.120 | 1 | 94000870 | stop gained | G/A | snv | 2.0E-05 | 7.0E-06 | 1 | |
| rs61753033 | 0.882 | 0.080 | 1 | 94008767 | missense variant | A/G | snv | 2.0E-05 | 1 | ||
| rs61751392 | 0.827 | 0.080 | 1 | 94063250 | missense variant | A/G | snv | 1.5E-04 | 1.7E-04 | 1 |