Source: GWASDB
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2256175 | 1.000 | 6 | 31412672 | intron variant | C/T | snv | 0.55 | 5 | |||
rs2596542 | 0.724 | 0.200 | 6 | 31398818 | upstream gene variant | C/T | snv | 0.41 | 5 | ||
rs1051794 | 0.925 | 0.120 | 6 | 31411332 | missense variant | G/A | snv | 0.34 | 0.35 | 4 | |
rs6910087 | 1.000 | 6 | 31409270 | intron variant | C/T | snv | 0.20 | 4 | |||
rs9266825 | 1.000 | 6 | 31415105 | 3 prime UTR variant | C/A;T | snv | 0.31; 8.1E-06 | 4 |