Source: GWASCAT
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1800961 | 0.851 | 0.160 | 20 | 44413724 | missense variant | C/T | snv | 3.1E-02 | 2.5E-02 | 17 | |
| rs16988991 | 1.000 | 0.080 | 20 | 44361137 | intron variant | G/A;C | snv | 1 | |||
| rs4812829 | 0.925 | 0.120 | 20 | 44360627 | intron variant | G/A | snv | 0.18 | 1 | ||
| rs6103716 | 1.000 | 0.080 | 20 | 44370990 | intron variant | A/C | snv | 0.37 | 1 | ||
| rs4810426 | 1.000 | 0.080 | 20 | 44373081 | intron variant | C/T | snv | 0.14 | 1 |