Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
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
rs4986791 0.501 0.714 9 117713324 missense variant C/T snp 5.7E-02 5.1E-02 108
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
rs1805087
MTR
0.538 0.679 1 236885200 missense variant A/G snp 0.20 0.21 75
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
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
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
rs1799793 0.585 0.500 19 45364001 missense variant C/A,T snp 7.1E-06; 0.29 0.27 51
rs1229984 0.622 0.393 4 99318162 missense variant T/C,G snp 0.90 0.94 50
rs1137101 0.605 0.679 1 65592830 missense variant A/G snp 0.51 0.53 41
rs1800566 0.605 0.571 16 69711242 missense variant G/A snp 0.25 0.21 41
rs17655 0.611 0.500 13 102875652 missense variant G/C snp 0.28 0.30 39
rs17879961 0.615 0.321 22 28725099 missense variant A/C,G snp 4.1E-03 1.1E-02 33
rs121434568 0.642 0.321 7 55191822 missense variant T/A,G snp 33
rs532358159 0.634 0.536 16 69711143 missense variant G/A snp 4.0E-06 30
rs121434569 0.667 0.321 7 55181378 missense variant C/T snp 2.8E-05 9.6E-05 29
rs121913273 0.638 0.357 3 179218294 missense variant G/A,C snp 29
rs28934578 0.647 0.357 17 7675088 missense variant snp 4.0E-06 27