Source: GWASDB
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs657152 | 0.882 | 0.200 | 9 | 133263862 | intron variant | A/C;T | snv | 14 | |||
| rs630014 | 9 | 133274306 | intron variant | G/A;C | snv | 9 | |||||
| rs507666 | 1.000 | 0.040 | 9 | 133273983 | intron variant | A/G | snv | 3 | |||
| rs2519093 | 0.882 | 0.200 | 9 | 133266456 | intron variant | T/C | snv | 2 | |||
| rs532436 | 1.000 | 0.080 | 9 | 133274414 | intron variant | A/G;T | snv | 1 | |||
| rs550057 | 0.925 | 0.080 | 9 | 133271182 | intron variant | T/A;C | snv | 1 |