| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs4986790 | 0.438 | 0.800 | 9 | 117713024 | missense variant | A/G;T | snv | 6.1E-02; 4.0E-06 | 223 | ||
| rs1065489 | 0.695 | 0.440 | 1 | 196740644 | missense variant | G/T | snv | 0.20 | 0.15 | 19 | |
| rs12085435 | 1.000 | 0.040 | 1 | 56949637 | missense variant | G/A | snv | 4.8E-02 | 5.5E-02 | 2 | |
| rs3753396 | 0.925 | 0.080 | 1 | 196726612 | synonymous variant | A/G | snv | 0.20 | 0.15 | 2 | |
| rs426736 | 1.000 | 0.040 | 1 | 196791287 | intron variant | A/G | snv | 0.28 | 2 |