| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1800562 | 0.435 | 0.880 | 6 | 26092913 | missense variant | G/A | snv | 3.3E-02 | 3.8E-02 | 262 | |
| rs1042714 | 0.597 | 0.640 | 5 | 148826910 | stop gained | G/C;T | snv | 0.68 | 54 | ||
| rs3779381 | 0.925 | 0.160 | 7 | 121326736 | intron variant | A/G | snv | 0.29 | 3 | ||
| rs112844193 | 0.925 | 0.160 | 1 | 245175674 | intron variant | C/T | snv | 6.6E-02 | 2 | ||
| rs112941217 | 0.925 | 0.160 | 1 | 156087626 | intron variant | T/C | snv | 2.7E-02 | 2 |