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