Source: GWASDB
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs3806156 | 0.827 | 0.280 | 6 | 32405921 | intron variant | G/A;T | snv | 5 | |||
| rs2076530 | 0.724 | 0.640 | 6 | 32396039 | missense variant | T/C | snv | 0.42 | 0.40 | 5 | |
| rs3817963 | 0.776 | 0.360 | 6 | 32400310 | intron variant | T/C | snv | 0.25 | 5 | ||
| rs2076533 | 0.882 | 0.200 | 6 | 32395750 | intron variant | C/T | snv | 0.40 | 3 | ||
| rs9268480 | 0.882 | 0.200 | 6 | 32396067 | synonymous variant | C/T | snv | 0.26 | 0.24 | 3 | |
| rs3763307 | 0.882 | 0.200 | 6 | 32406845 | non coding transcript exon variant | A/T | snv | 0.24 | 3 |