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
rs25487 0.485 0.679 19 43551574 missense variant T/C snp 0.68 0.72 119
rs11540654 0.492 0.679 17 7676040 missense variant C/A,G,T snp 4.8E-05 3.2E-05 117
rs1045642 0.520 0.714 7 87509329 synonymous variant A/G,T snp 0.50 0.56 108
rs1799782 0.523 0.607 19 43553422 stop gained G/A snp 9.5E-02 7.1E-02 84
rs13181 0.525 0.536 19 45351661 stop gained T/A,G snp 4.0E-06; 0.32 0.32 82
rs2910164 0.525 0.750 5 160485411 mature miRNA variant C/G snp 0.71; 4.1E-06 0.71 82
rs4880 0.536 0.643 6 159692840 missense variant A/G snp 0.48 0.47 81
rs1052133 0.533 0.643 3 9757089 missense variant C/G snp 0.27 0.22 77
rs121913279 0.559 0.536 3 179234297 missense variant A/G,T snp 4.0E-06; 4.0E-06 68
rs861539 0.561 0.464 14 103699416 missense variant G/A snp 0.29 0.29 60
rs121434592 0.582 0.500 14 104780214 missense variant C/T snp 4.0E-06 56
rs2032582 0.602 0.500 7 87531302 missense variant A/C,T snp 0.54; 3.8E-02 0.64; 2.5E-02 54
rs1048943 0.572 0.571 15 74720644 missense variant T/C snp 0.11 5.0E-02 53
rs104886003 0.580 0.393 3 179218303 missense variant G/A,C snp 4.0E-06 52
rs895819 0.667 0.286 19 13836478 non coding transcript exon variant T/C snp 0.34 0.38 25
rs752021744 0.699 0.429 3 138759306 T/C snp 1.2E-05 21
rs10735810
VDR
0.692 0.357 12 47879112 start lost snp 17
rs61764370 0.692 0.250 12 25207290 3 prime UTR variant A/C snp 5.3E-02 16
rs11568820 0.744 0.179 12 47908762 intron variant C/T snp 0.36 11
rs1950902 0.756 0.214 14 64415662 missense variant A/G snp 0.83 0.81 10