Source: GWASDB
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs20541 | 0.585 | 0.720 | 5 | 132660272 | missense variant | A/G | snv | 0.72 | 0.77 | 5 | |
rs6871536 | 0.827 | 0.160 | 5 | 132634182 | intron variant | T/C | snv | 0.24 | 2 | ||
rs1295685 | 0.790 | 0.160 | 5 | 132660753 | 3 prime UTR variant | A/G | snv | 0.81 | 2 | ||
rs1295686 | 0.882 | 0.160 | 5 | 132660151 | intron variant | T/A;C | snv | 0.68 | 2 | ||
rs2240032 | 1.000 | 0.080 | 5 | 132641435 | intron variant | C/G;T | snv | 1 |