| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs193922219 | 0.763 | 0.280 | 15 | 48446701 | splice region variant | C/A;T | snv | 9 | |||
| rs1465567 | 0.882 | 0.040 | 5 | 38370435 | missense variant | T/C | snv | 0.20 | 0.25 | 3 | |
| rs1553303352 | 0.882 | 0.120 | 1 | 218437368 | missense variant | C/T | snv | 3 | |||
| rs113710653 | 0.925 | 0.080 | 21 | 46161921 | missense variant | C/T | snv | 6.5E-02 | 6.1E-02 | 2 | |
| rs777763524 | 1.000 | 0.040 | 2 | 215431961 | missense variant | C/T | snv | 8.0E-06 | 7.0E-06 | 1 | |
| rs143881017 | 1.000 | 0.040 | 14 | 21033870 | missense variant | C/A;T | snv | 1.6E-05; 7.4E-04 | 1 |