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
rs1800734 0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 30
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs13281615 0.716 0.360 8 127343372 intron variant A/G snv 0.43 18
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1950902 0.776 0.240 14 64415662 missense variant A/G snv 0.83 0.83 11