Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4925 0.677 0.560 10 104263031 missense variant C/A snv 0.25 0.23 28
rs156697 0.672 0.560 10 104279427 missense variant A/G;T snv 0.35 25
rs866838052 0.851 0.160 7 143267618 missense variant C/A snv 6
rs62527607 0.827 0.160 8 103141321 non coding transcript exon variant G/T snv 0.14 5
rs11980379 0.882 0.120 7 50402283 3 prime UTR variant T/C snv 0.25 3
rs189434316 0.925 0.120 14 92231568 intergenic variant A/T snv 4.1E-02 2
rs2393732 0.925 0.120 10 62007470 intron variant G/A snv 0.15 2
rs4948488 0.925 0.120 10 61925395 intron variant C/A;T snv 2