Source: GWASCAT
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2293751 | 1.000 | 0.040 | 6 | 31940060 | intron variant | G/A;C | snv | 2 | |||
| rs116385615 | 1.000 | 0.040 | 6 | 31913532 | intron variant | T/C | snv | 2 | |||
| rs142520578 | 1.000 | 0.040 | 6 | 31894038 | intron variant | G/A | snv | 2 | |||
| rs389883 | 0.827 | 0.200 | 6 | 31979683 | non coding transcript exon variant | G/T | snv | 0.80 | 2 | ||
| rs2734325 | 1.000 | 0.040 | 6 | 31977869 | intron variant | C/T | snv | 0.27 | 1 |