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
rs4680 0.484 0.821 22 19963748 missense variant G/A snp 0.46 0.45 155
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
rs1695 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 100
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
rs1805087
MTR
0.538 0.679 1 236885200 missense variant A/G snp 0.20 0.21 75
rs121913529 0.559 0.393 12 25245350 missense variant C/A,G,T snp 4.0E-06 70
rs1800629
TNF
0.549 0.786 6 31575254 intergenic variant G/A snp 0.12 0.15 69
rs121913279 0.559 0.536 3 179234297 missense variant A/G,T snp 4.0E-06; 4.0E-06 68
rs28934576 0.563 0.536 17 7673802 missense variant C/A,G,T snp 4.0E-06; 1.6E-05 64
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
rs1042522 0.563 0.643 17 7676154 stop gained G/C,T snp 0.67 0.62 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
rs5498 0.570 0.679 19 10285007 missense variant A/G snp 0.44 0.36 53
rs104886003 0.580 0.393 3 179218303 missense variant G/A,C snp 4.0E-06 52
rs2736100 0.596 0.571 5 1286401 intron variant C/A snp 0.53 52
rs1799793 0.585 0.500 19 45364001 missense variant C/A,T snp 7.1E-06; 0.29 0.27 51