Source: GWASDB
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1635852 | 0.882 | 0.160 | 7 | 28149792 | intron variant | T/C | snv | 0.42 | 2 | ||
rs1029534 | 7 | 28149464 | intron variant | T/C;G | snv | 1 | |||||
rs1708299 | 7 | 28150327 | intron variant | A/G | snv | 0.77 | 1 | ||||
rs849141 | 0.851 | 0.240 | 7 | 28145472 | intron variant | A/G | snv | 0.78 | 1 |