| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121909210 | 0.708 | 0.200 | 5 | 136046406 | missense variant | C/A;T | snv | 4.0E-06; 4.0E-06 | 15 | ||
| rs121909715 | 0.790 | 0.160 | 9 | 121310819 | missense variant | G/A;T | snv | 4.0E-06 | 8 | ||
| rs756465037 | 0.807 | 0.200 | 3 | 46439392 | missense variant | C/G | snv | 8.0E-06 | 7.0E-06 | 6 | |
| rs121909212 | 0.807 | 0.160 | 5 | 136055770 | missense variant | C/A;G;T | snv | 3.2E-04; 3.2E-05; 3.6E-05 | 6 | ||
| rs267607109 | 0.827 | 0.160 | 5 | 136056754 | missense variant | C/A | snv | 5 | |||
| rs267607110 | 0.851 | 0.160 | 5 | 136056769 | missense variant | C/A | snv | 4 | |||
| rs80358223 | 0.925 | 0.160 | 1 | 58576805 | stop gained | G/A | snv | 7.0E-06 | 2 | ||
| rs80358225 | 1.000 | 0.120 | 1 | 58576648 | stop gained | G/T | snv | 2 | |||
| rs1282483375 | 1.000 | 0.120 | 1 | 58576757 | missense variant | G/A | snv | 1 | |||
| rs190800473 | 1.000 | 0.120 | 1 | 58576606 | missense variant | T/C | snv | 4.2E-06 | 7.0E-06 | 1 | |
| rs80358224 | 1.000 | 0.120 | 1 | 58576538 | stop gained | G/A | snv | 1 | |||
| rs80358226 | 1.000 | 0.120 | 1 | 58577155 | start lost | A/C;G;T | snv | 1 | |||
| rs80358227 | 1.000 | 0.120 | 1 | 58576802 | missense variant | A/T | snv | 1 | |||
| rs80358228 | 1.000 | 0.120 | 1 | 58576600 | missense variant | A/G | snv | 1 |