Source: GWASCAT
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11603150 | 11 | 36352319 | intron variant | T/C | snv | 0.25 | 1 | ||||
rs67184556 | 11 | 36306244 | intron variant | C/T | snv | 0.30 | 1 | ||||
rs7114403 | 11 | 36340057 | intron variant | T/A;G | snv | 1 | |||||
rs62621409 | 11 | 36437447 | missense variant | A/G | snv | 3.9E-02 | 3.5E-02 | 3 |