Source: GWASDB
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs12000 | 0.925 | 0.160 | 6 | 28259658 | missense variant | A/G | snv | 0.28 | 0.34 | 1 | |
| rs1635 | 1.000 | 0.040 | 6 | 28259826 | missense variant | C/A;T | snv | 0.12 | 1 | ||
| rs1233710 | 1.000 | 0.040 | 6 | 28247668 | intron variant | C/T | snv | 0.13 | 1 | ||
| rs2235359 | 0.925 | 0.160 | 6 | 28247863 | intron variant | T/G | snv | 0.20 | 1 |