| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1114167433 | 0.925 | 0.200 | 22 | 26607934 | missense variant | G/T | snv | 2 | |||
| rs200090198 | 1.000 | 0.040 | 16 | 2326214 | missense variant | G/A;C;T | snv | 7.2E-05; 2.5E-04 | 1 | ||
| rs201955122 | 1.000 | 0.040 | 16 | 2279097 | missense variant | C/T | snv | 1.2E-04 | 7.0E-05 | 1 | |
| rs748819386 | 1.000 | 0.040 | 16 | 2295596 | missense variant | G/A | snv | 1.2E-05 | 3.5E-05 | 1 | |
| rs1114167432 | 1.000 | 0.040 | 22 | 26599492 | stop lost | A/G | snv | 1 |