Source: GWASCAT ×
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7127214 | 0.807 | 0.120 | 11 | 36322143 | intron variant | C/G;T | snv | 6 | |||
rs72698115 | 0.807 | 0.120 | 1 | 154406893 | intron variant | A/C | snv | 7.2E-02 | 6 | ||
rs73300638 | 0.807 | 0.120 | 7 | 28147725 | intron variant | A/C;G | snv | 6 | |||
rs7775055 | 0.790 | 0.200 | 6 | 32690139 | TF binding site variant | T/C | snv | 6.2E-02 | 6 | ||
rs7909519 | 0.807 | 0.120 | 10 | 6047878 | intron variant | T/G | snv | 7.2E-02 | 6 | ||
rs79893749 | 0.807 | 0.120 | 3 | 46212159 | intron variant | C/T | snv | 0.10 | 6 |