Source: GWASCAT
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10503253 | 0.851 | 0.040 | 8 | 4323322 | intron variant | C/A | snv | 0.18 | 5 | ||
| rs6558872 | 0.882 | 0.040 | 8 | 4380617 | intron variant | G/A;C | snv | 3 | |||
| rs10046758 | 1.000 | 0.040 | 8 | 4326648 | non coding transcript exon variant | C/G;T | snv | 1 | |||
| rs10503256 | 1.000 | 0.040 | 8 | 4356657 | intron variant | A/G | snv | 0.57 | 1 | ||
| rs12541020 | 1.000 | 0.040 | 8 | 4960070 | intron variant | T/A;C | snv | 1 | |||
| rs13261217 | 1.000 | 0.040 | 8 | 4325535 | non coding transcript exon variant | A/G | snv | 0.26 | 1 | ||
| rs139425113 | 1.000 | 0.040 | 8 | 4323090 | intron variant | A/-;AA;AAA | delins | 1 |