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
rs1800562 0.463 0.714 6 26092913 missense variant G/A snp 3.3E-02 3.8E-02 175
rs397507444 0.457 0.714 1 11794407 missense variant T/G snp 169
rs1799945 0.475 0.679 6 26090951 missense variant C/G snp 0.11 9.9E-02 152
rs1799983 0.475 0.786 7 150999023 missense variant T/A,G snp 0.75 0.76 138
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
rs1801133 0.533 0.714 1 11796321 missense variant G/A snp 0.31 0.26 86
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
rs671 0.593 0.464 12 111803962 missense variant G/A snp 1.9E-02 1.3E-02 61
rs861539 0.561 0.464 14 103699416 missense variant G/A snp 0.29 0.29 60
rs7903146 0.596 0.536 10 112998590 intron variant C/G,T snp 0.26 59
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
rs1801131 0.599 0.607 1 11794419 missense variant T/G snp 0.29 0.26 49
rs731236
VDR
0.605 0.571 12 47844974 synonymous variant A/G snp 0.33 0.33 39
rs351855 0.642 0.357 5 177093242 missense variant G/A snp 0.33 0.27 35