Source: GWASCAT
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12670798 | 1.000 | 0.040 | 7 | 21567734 | intron variant | T/C | snv | 0.26 | 3 | ||
rs66476925 | 7 | 21571781 | intron variant | G/A;C;T | snv | 4.4E-06; 0.17; 4.4E-06 | 3 | ||||
rs56130071 | 7 | 21559135 | intron variant | G/C | snv | 0.18 | 2 | ||||
rs73066485 | 7 | 21572352 | intron variant | T/A;G | snv | 1 |