Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022 0.407 0.786 7 140753336 missense variant snp 4.0E-06 267
rs397507444 0.457 0.714 1 11794407 missense variant T/G snp 169
rs4680 0.484 0.821 22 19963748 missense variant G/A snp 0.46 0.45 155
rs4986790 0.465 0.750 9 117713024 missense variant A/G,T snp 6.1E-02; 4.0E-06 6.7E-02 146
rs25487 0.485 0.679 19 43551574 missense variant T/C snp 0.68 0.72 119
rs1799782 0.523 0.607 19 43553422 stop gained G/A snp 9.5E-02 7.1E-02 84
rs1052133 0.533 0.643 3 9757089 missense variant C/G snp 0.27 0.22 77
rs121913529 0.559 0.393 12 25245350 missense variant C/A,G,T snp 4.0E-06 70
rs121434592 0.582 0.500 14 104780214 missense variant C/T snp 4.0E-06 56
rs1048943 0.572 0.571 15 74720644 missense variant T/C snp 0.11 5.0E-02 53
rs2736100 0.596 0.571 5 1286401 intron variant C/A snp 0.53 52
rs121913530 0.615 0.321 12 25245351 missense variant C/A,G,T snp 39
rs121434568 0.642 0.321 7 55191822 missense variant T/A,G snp 33
rs1333049 0.715 0.286 9 22125504 intergenic variant G/C snp 0.41 30
rs121434569 0.667 0.321 7 55181378 missense variant C/T snp 2.8E-05 9.6E-05 29
rs759728549 0.679 0.214 17 7676223 stop lost T/C snp 8.0E-06 26
rs28934575 0.673 0.321 17 7674230 missense variant C/A,G,T snp 25
rs401681 0.679 0.464 5 1321972 intron variant C/T snp 0.48 22
rs2736098 0.679 0.286 5 1293971 synonymous variant C/T snp 0.29 0.22 22
rs397514495 0.707 0.286 17 7675070 missense variant C/A,T snp 1.2E-05 3.2E-05 22
rs752021744 0.699 0.429 3 138759306 T/C snp 1.2E-05 21
rs16969968 0.699 0.214 15 78590583 missense variant G/A snp 0.26 0.24 20
rs4977756 0.734 0.357 9 22068653 intron variant G/A snp 0.64 16
rs121918464 0.756 0.321 12 112450406 missense variant G/A,C snp 15
rs2853676 0.724 0.214 5 1288432 intron variant T/A,C snp 0.76 15