Source: GWASCAT
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2305480 | 0.763 | 0.280 | 17 | 39905943 | missense variant | G/A | snv | 0.40 | 0.35 | 4 | |
rs2290400 | 0.790 | 0.360 | 17 | 39909987 | intron variant | T/C | snv | 0.48 | 3 | ||
rs869402 | 0.925 | 0.160 | 17 | 39911790 | intron variant | T/A;C | snv | 2 | |||
rs1008723 | 0.925 | 0.160 | 17 | 39910014 | intron variant | G/C;T | snv | 1 | |||
rs11078927 | 0.925 | 0.080 | 17 | 39908152 | intron variant | C/T | snv | 0.40 | 0.35 | 1 | |
rs2305479 | 0.882 | 0.160 | 17 | 39905964 | missense variant | C/T | snv | 0.43 | 0.39 | 1 | |
rs4795400 | 0.925 | 0.080 | 17 | 39910767 | intron variant | C/T | snv | 0.36 | 1 | ||
rs7216389 | 0.732 | 0.440 | 17 | 39913696 | intron variant | C/T | snv | 0.60 | 1 | ||
rs921650 | 1.000 | 0.080 | 17 | 39912823 | intron variant | G/A | snv | 0.60 | 1 | ||
rs9303280 | 1.000 | 0.080 | 17 | 39917778 | non coding transcript exon variant | T/A;C | snv | 1 |