Source: GWASCAT
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1470579 | 0.925 | 0.160 | 3 | 185811292 | intron variant | A/C | snv | 0.46 | 4 | ||
| rs11705729 | 1.000 | 0.080 | 3 | 185789511 | intron variant | A/T | snv | 0.45 | 2 | ||
| rs11927381 | 1.000 | 0.080 | 3 | 185790803 | intron variant | T/C | snv | 0.45 | 1 | ||
| rs13092876 | 1.000 | 0.080 | 3 | 185777532 | intron variant | G/A | snv | 0.45 | 1 | ||
| rs1374910 | 1.000 | 0.080 | 3 | 185813873 | intron variant | C/T | snv | 9.5E-02 | 1 | ||
| rs4402960 | 0.724 | 0.400 | 3 | 185793899 | intron variant | G/T | snv | 0.38 | 1 | ||
| rs4414887 | 1.000 | 0.080 | 3 | 185789104 | intron variant | C/T | snv | 0.41 | 1 | ||
| rs6769511 | 0.925 | 0.120 | 3 | 185812502 | intron variant | T/C | snv | 0.46 | 1 | ||
| rs71320321 | 1.000 | 0.080 | 3 | 185801319 | intron variant | G/A | snv | 0.39 | 1 | ||
| rs7633675 | 1.000 | 0.080 | 3 | 185792825 | intron variant | T/G | snv | 0.45 | 1 | ||
| rs7637773 | 1.000 | 0.080 | 3 | 185797847 | intron variant | G/A | snv | 0.38 | 1 | ||
| rs7640539 | 1.000 | 0.080 | 3 | 185795508 | intron variant | T/A | snv | 0.39 | 1 | ||
| rs7651090 | 0.925 | 0.080 | 3 | 185795604 | intron variant | A/G | snv | 0.39 | 1 |