| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121909231 | 0.667 | 0.600 | 10 | 87961095 | stop gained | C/A;T | snv | 29 | |||
| rs121913237 | 0.611 | 0.560 | 1 | 114716126 | missense variant | C/A;G;T | snv | 8.0E-06 | 12 | ||
| rs869320686 | 0.882 | 22 | 20990476 | missense variant | G/A | snv | 4 | ||||
| rs2435357 | 0.790 | 0.240 | 10 | 43086608 | intron variant | T/C | snv | 0.79 | 3 | ||
| rs267606920 | 0.882 | 0.160 | 1 | 114713911 | missense variant | C/T | snv | 7.0E-06 | 2 | ||
| rs121912679 | 1.000 | 0.040 | 2 | 157761077 | missense variant | C/T | snv | 1 | |||
| rs118203918 | 0.882 | 0.160 | 6 | 53016099 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
| rs121908332 | 0.882 | 0.240 | 8 | 139618677 | missense variant | C/G;T | snv | 1 | |||
| rs150419186 | 1.000 | 0.160 | 22 | 20989659 | stop gained | C/A;G;T | snv | 4.0E-06; 1.2E-05; 7.2E-05 | 1 | ||
| rs587777178 | 0.925 | 0.080 | 22 | 20995865 | missense variant | C/T | snv | 4.4E-05 | 6.3E-05 | 1 | |
| rs869025573 | 1.000 | 0.160 | 1 | 114716090 | missense variant | A/T | snv | 1 | |||
| rs267606956 | 1.000 | 19 | 49862424 | stop gained | C/A;T | snv | 1 |