Source: GWASDB
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11532322 | 1.000 | 0.040 | 12 | 123246876 | intron variant | A/G;T | snv | 1 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11532322 | 1.000 | 0.040 | 12 | 123246876 | intron variant | A/G;T | snv | 1 |