Source: GWASDB
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11105354 | 12 | 89632746 | intron variant | A/G | snv | 0.15 | 1 | ||||
rs2681492 | 0.925 | 0.040 | 12 | 89619312 | intron variant | T/C;G | snv | 3 | |||
rs2681472 | 0.882 | 0.080 | 12 | 89615182 | intron variant | A/G | snv | 0.14 | 4 | ||
rs17249754 | 0.882 | 0.120 | 12 | 89666809 | intron variant | G/A | snv | 0.15 | 3 |