Source: BEFREE
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7216389 | 0.732 | 0.440 | 17 | 39913696 | intron variant | C/T | snv | 0.60 | 12 | ||
rs2305480 | 0.763 | 0.280 | 17 | 39905943 | missense variant | G/A | snv | 0.40 | 0.35 | 5 | |
rs2290400 | 0.790 | 0.360 | 17 | 39909987 | intron variant | T/C | snv | 0.48 | 4 | ||
rs11078927 | 0.925 | 0.080 | 17 | 39908152 | intron variant | C/T | snv | 0.40 | 0.35 | 2 | |
rs11078928 | 0.925 | 0.160 | 17 | 39908216 | splice acceptor variant | T/A;C | snv | 0.40 | 1 | ||
rs4795400 | 0.925 | 0.080 | 17 | 39910767 | intron variant | C/T | snv | 0.36 | 1 |