| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs189261858 | 0.776 | 0.160 | 14 | 81143407 | missense variant | G/A;T | snv | 2.3E-04 | 8 | ||
| rs1294870139 | 0.925 | 0.120 | 14 | 81143638 | missense variant | T/C | snv | 8.0E-06 | 2 | ||
| rs139892516 | 0.925 | 0.120 | 14 | 81143649 | missense variant | C/G;T | snv | 4.0E-06; 2.8E-05 | 2 |