Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34536443 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 20
rs72928038 0.695 0.360 6 90267049 intron variant G/A snv 0.11 19
rs4409785 0.752 0.240 11 95578258 intron variant T/C snv 0.13 12
rs60600003 0.827 0.120 7 37342861 intron variant T/C;G snv 7
rs10797431 0.851 0.080 1 2569783 non coding transcript exon variant G/T snv 0.42 5