| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs57077886 | 0.776 | 0.240 | 1 | 156114947 | missense variant | C/T | snv | 9 | |||
| rs147105770 | 0.776 | 0.280 | 16 | 13935697 | missense variant | C/G;T | snv | 1.2E-05; 6.4E-05 | 8 | ||
| rs150840924 | 0.807 | 0.240 | 1 | 156136359 | missense variant | C/T | snv | 8.0E-06 | 7.0E-06 | 7 | |
| rs121913028 | 0.851 | 0.400 | 19 | 45414870 | missense variant | G/A;C | snv | 1.2E-05; 1.6E-05 | 4 | ||
| rs1555468482 | 0.882 | 0.240 | 16 | 13935663 | frameshift variant | C/- | del | 3 | |||
| rs121434575 | 0.925 | 0.240 | 13 | 102868152 | missense variant | T/C | snv | 2 | |||
| rs121434323 | 0.925 | 0.160 | 5 | 60890964 | stop gained | G/C;T | snv | 4.0E-06 | 2 | ||
| rs886039224 | 1.000 | 0.160 | 19 | 45414887 | stop gained | T/A | snv | 1 | |||
| rs1057518910 | 1.000 | 0.160 | 10 | 49500634 | missense variant | A/G | snv | 4.0E-06 | 1 | ||
| rs752712823 | 1.000 | 0.160 | 10 | 49500628 | missense variant | T/C | snv | 4.0E-06 | 1 | ||
| rs774175886 | 1.000 | 0.160 | 10 | 49500616 | missense variant | A/C | snv | 4.0E-05 | 2.8E-05 | 1 |