Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1413711 0.882 0.200 6 43772941 intron variant T/A;C snv 3
rs833070 0.776 0.440 6 43774889 non coding transcript exon variant T/C snv 0.58 11
rs1005230 0.827 0.040 6 43768759 upstream gene variant T/C snv 0.60 5
rs3025021 0.882 0.160 6 43781426 non coding transcript exon variant T/C snv 0.70 4
rs374057152 0.925 0.200 6 43777592 missense variant T/C snv 4.0E-06 1.4E-05 3
rs1229919945 1.000 0.040 6 43782041 missense variant T/C snv 1
rs833069 0.851 0.200 6 43774842 non coding transcript exon variant T/C;G snv 5
rs3025010 6 43779840 non coding transcript exon variant T/C;G snv 1
rs1188254133 0.851 0.240 6 43781990 missense variant T/G snv 7.0E-06 4