Source: GWASDB
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7903146 | 0.554 | 0.680 | 10 | 112998590 | intron variant | C/G;T | snv | 8 | |||
rs12255372 | 0.667 | 0.480 | 10 | 113049143 | intron variant | G/A;T | snv | 3 | |||
rs7904519 | 0.763 | 0.240 | 10 | 113014168 | intron variant | A/G | snv | 0.55 | 2 | ||
rs11196172 | 0.708 | 0.200 | 10 | 112967084 | intron variant | G/A | snv | 0.13 | 1 | ||
rs11196174 | 1.000 | 0.080 | 10 | 112974337 | intron variant | A/C;G | snv | 1 | |||
rs11196175 | 0.925 | 0.160 | 10 | 112976855 | intron variant | T/C | snv | 0.20 | 1 | ||
rs7900150 | 0.882 | 0.160 | 10 | 113034064 | intron variant | T/A;C | snv | 0.54 | 1 |