Source: GWASDB
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1544791 | 1.000 | 0.080 | 5 | 60143255 | intron variant | T/A;C | snv | 1 | |||
| rs1588265 | 1.000 | 0.080 | 5 | 60073967 | intron variant | A/G;T | snv | 1 | |||
| rs2548659 | 1.000 | 0.080 | 5 | 60088059 | intron variant | A/G | snv | 0.28 | 1 | ||
| rs983280 | 1.000 | 0.080 | 5 | 60149310 | intron variant | C/T | snv | 0.68 | 1 |