Source: GWASCAT
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1874124 | 1 | 220801995 | intron variant | C/T | snv | 0.11 | 2 | ||||
rs2642442 | 1 | 220800221 | intron variant | C/T | snv | 0.73 | 2 | ||||
rs2807834 | 1 | 220797251 | intron variant | T/C;G | snv | 2 | |||||
rs2642438 | 1 | 220796686 | missense variant | A/G | snv | 0.75 | 0.78 | 6 |