Source: GWASCAT
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs16856823 | 2 | 169343942 | intron variant | A/T | snv | 4.6E-02 | 3 | ||||
rs147287428 | 2 | 169206713 | missense variant | C/T | snv | 2.7E-04 | 4.7E-04 | 2 | |||
rs200309784 | 2 | 169347589 | intron variant | AA/-;A;AAA;AAAA | delins | 2 | |||||
rs4667594 | 2 | 169151996 | intron variant | T/A;C | snv | 2 | |||||
rs35472707 | 2 | 169139071 | intron variant | C/T | snv | 4.1E-02 | 1 | ||||
rs3770636 | 2 | 169346323 | intron variant | T/G | snv | 4.6E-02 | 1 | ||||
rs3815573 | 2 | 169155942 | intron variant | A/G;T | snv | 1 | |||||
rs57989581 | 2 | 169337949 | intron variant | C/A | snv | 2.6E-02 | 1 | ||||
rs60641214 | 2 | 169342782 | intron variant | A/T | snv | 0.25 | 1 | ||||
rs755631 | 2 | 169150430 | intron variant | A/C | snv | 0.49 | 1 |