Source: GWASCAT
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11718418 | 3 | 172053964 | intron variant | A/G | snv | 0.55 | 1 | ||||
rs4243400 | 3 | 172253069 | intron variant | A/G | snv | 0.60 | 1 | ||||
rs4535251 | 3 | 172208583 | intron variant | T/A;C | snv | 1 | |||||
rs4894539 | 3 | 172281493 | intron variant | G/T | snv | 0.53 | 1 | ||||
rs62281815 | 3 | 172252520 | intron variant | A/T | snv | 0.41 | 1 | ||||
rs7652177 | 3 | 172251287 | missense variant | C/G | snv | 0.54 | 0.61 | 1 | |||
rs4894797 | 3 | 172065756 | intron variant | G/A | snv | 0.47 | 2 |