Source: GWASDB
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3132946 | 0.882 | 0.240 | 6 | 32222251 | intron variant | A/G | snv | 0.91 | 3 | ||
rs422951 | 0.807 | 0.280 | 6 | 32220606 | missense variant | T/C | snv | 0.40 | 0.40 | 2 | |
rs3131294 | 1.000 | 0.080 | 6 | 32212369 | intron variant | A/G | snv | 0.91 | 1 | ||
rs438475 | 1.000 | 0.080 | 6 | 32218468 | intron variant | G/A;C | snv | 1 |