| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs199589947 | 0.882 | 0.280 | 3 | 45496316 | missense variant | C/A | snv | 3.0E-04 | 2.5E-04 | 3 | |
| rs863223921 | 0.925 | 0.280 | 10 | 100989406 | missense variant | A/G | snv | 4.0E-06 | 1.4E-05 | 3 | |
| rs200089613 | 0.925 | 0.280 | 5 | 140698056 | missense variant | G/A;T | snv | 8.0E-05; 3.7E-04 | 2 | ||
| rs376177973 | 0.925 | 0.280 | 5 | 140697311 | missense variant | G/A;T | snv | 2.4E-05; 8.0E-06 | 2 | ||
| rs397515410 | 0.925 | 0.280 | 5 | 140695810 | missense variant | C/G | snv | 2 | |||
| rs374161061 | 1.000 | 0.280 | 5 | 119499543 | missense variant | A/G | snv | 1.2E-04 | 2.1E-05 | 2 | |
| rs1468024757 | 1.000 | 0.280 | 5 | 140676749 | missense variant | C/G | snv | 4.0E-06 | 1 | ||
| rs755882900 | 1.000 | 0.280 | 5 | 140677102 | missense variant | C/A | snv | 4.0E-06 | 1 | ||
| rs786205560 | 1.000 | 0.280 | 3 | 45419670 | missense variant | A/C | snv | 1 | |||
| rs773142741 | 1.000 | 0.280 | 3 | 45488769 | missense variant | A/G | snv | 8.0E-06 | 1 | ||
| rs141315771 | 1.000 | 0.280 | 10 | 100993257 | missense variant | G/A | snv | 2.8E-05 | 2.8E-05 | 1 |