Source: GWASCAT
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs757318 | 19 | 18709498 | intron variant | C/A;G;T | snv | 3 | |||||
rs2003476 | 19 | 18695858 | intron variant | T/C | snv | 0.53 | 2 | ||||
rs10221489 | 19 | 18716165 | intron variant | C/T | snv | 0.38 | 1 | ||||
rs11668500 | 19 | 18725864 | intron variant | C/A;G;T | snv | 1 | |||||
rs8112818 | 19 | 18701975 | intron variant | A/C;G | snv | 1 |