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