Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57