Source: GWASCAT
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs6795735 | 0.882 | 0.120 | 3 | 64719689 | intron variant | C/A;G;T | snv | 6 | |||
| rs2371767 | 3 | 64732582 | intron variant | G/C | snv | 0.38 | 5 | ||||
| rs9860730 | 3 | 64715470 | intron variant | A/G | snv | 0.50 | 3 | ||||
| rs66815886 | 3 | 64717718 | intron variant | G/T | snv | 0.37 | 1 | ||||
| rs7372321 | 3 | 64728139 | intron variant | T/A;C;G | snv | 1 | |||||
| rs76699125 | 3 | 64715859 | intron variant | T/C | snv | 4.9E-02 | 1 |