Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1635852 0.882 0.160 7 28149792 intron variant T/C snv 0.42 4
rs849140 0.851 0.240 7 28144083 intron variant T/C snv 0.58 3
rs864745 0.763 0.320 7 28140937 intron variant T/C snv 0.41 3
rs10245867 0.925 0.080 7 28102567 intron variant G/T snv 0.37 2
rs702814 1.000 0.080 7 28133113 intron variant C/T snv 0.37 2
rs12531540 1.000 0.080 7 28123055 intron variant C/T snv 0.36 1
rs849141 0.851 0.240 7 28145472 intron variant A/G snv 0.78 1
rs849142 0.807 0.240 7 28146272 intron variant T/C snv 0.39 1