Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28929474 0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 37
rs1047891 0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 34
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 12
rs11187838 10 94278929 non coding transcript exon variant G/A snv 0.44 3
rs7996639 13 96366836 intron variant G/A snv 0.50 3