Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs1799971 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs324420 0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs6277 0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38 36
rs1076560 0.776 0.120 11 113412966 intron variant C/A snv 0.16 11
rs279858 0.851 0.080 4 46312576 synonymous variant T/C snv 0.40 0.38 8
rs886205 0.827 0.360 12 111766623 intron variant A/G snv 0.35 8
rs1126671 0.851 0.120 4 99127263 missense variant T/C snv 0.76 0.75 5
rs1042363 0.882 0.080 6 151356693 3 prime UTR variant T/C snv 4
rs1800759 0.925 0.120 4 99144358 intron variant T/G snv 0.49 4