| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs4149584 | 0.683 | 0.440 | 12 | 6333477 | missense variant | C/G;T | snv | 4.0E-06; 1.3E-02 | 24 | ||
| rs28940578 | 0.716 | 0.400 | 16 | 3243405 | missense variant | C/T | snv | 1.4E-04 | 6.3E-05 | 16 | |
| rs121908147 | 0.807 | 0.280 | 1 | 247424041 | missense variant | G/A;C | snv | 8.3E-03; 4.0E-06 | 7 | ||
| rs1423560438 | 0.882 | 0.080 | 6 | 137875748 | stop gained | C/T | snv | 3 | |||
| rs779189628 | 0.925 | 0.120 | 2 | 201284885 | missense variant | A/G | snv | 4.0E-06 | 2 | ||
| rs141389711 | 1.000 | 0.040 | 1 | 247434206 | missense variant | G/A | snv | 8.4E-05 | 6.3E-05 | 1 | |
| rs750572947 | 1.000 | 0.040 | 15 | 77037147 | missense variant | G/A | snv | 1.1E-04 | 7.0E-05 | 1 |