| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11575937 | 0.653 | 0.480 | 1 | 156136985 | missense variant | G/A;T | snv | 29 | |||
| rs397515453 | 0.752 | 0.440 | 5 | 68296301 | missense variant | C/T | snv | 11 | |||
| rs121909244 | 0.776 | 0.160 | 3 | 12434111 | missense variant | C/A;T | snv | 4.0E-06 | 11 | ||
| rs57520892 | 0.776 | 0.200 | 1 | 156137204 | missense variant | G/A;C | snv | 4.1E-05 | 8 | ||
| rs563539429 | 0.851 | 0.240 | 9 | 136677540 | missense variant | C/A;G;T | snv | 4.1E-06; 8.1E-06; 1.5E-03 | 5 | ||
| rs56657623 | 0.827 | 0.120 | 1 | 156138540 | missense variant | G/A | snv | 1.6E-05 | 7.0E-06 | 5 | |
| rs72551363 | 0.882 | 0.080 | 3 | 12417048 | missense variant | T/A | snv | 3 | |||
| rs121912493 | 0.925 | 0.080 | 1 | 156136374 | missense variant | G/A | snv | 2.1E-05 | 2 | ||
| rs121909245 | 0.925 | 0.080 | 3 | 12392701 | missense variant | T/A | snv | 2 | |||
| rs541978825 | 1.000 | 0.080 | 9 | 136676673 | missense variant | A/G | snv | 2.4E-05 | 1 | ||
| rs746782259 | 1.000 | 0.080 | 1 | 161170688 | missense variant | T/A | snv | 4.0E-06 | 1 |