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-06 262
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
rs1800562 0.463 0.714 6 26092913 missense variant G/A snp 3.3E-02 3.8E-02 154
rs4986790 0.465 0.750 9 117713024 missense variant A/G,T snp 6.1E-02; 4.0E-06 6.7E-02 144
rs1799983 0.475 0.786 7 150999023 missense variant T/A,G snp 0.75 0.76 138
rs1799945 0.475 0.679 6 26090951 missense variant C/G snp 0.11 9.9E-02 135
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-05 116
rs1045642 0.520 0.714 7 87509329 synonymous variant A/G,T snp 0.50 0.56 108
rs4986791 0.501 0.714 9 117713324 missense variant C/T snp 5.7E-02 5.1E-02 108
rs1695 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 100
rs1801133 0.533 0.714 1 11796321 missense variant G/A snp 0.31 0.26 84
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
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
rs1801282 0.543 0.679 3 12351626 missense variant C/G snp 0.11 1.0E-01 75
rs1805192 0.545 0.679 3 12379739 missense variant C/G snp 75
rs121913529 0.559 0.393 12 25245350 missense variant C/A,G,T snp 4.0E-06 61
rs1801394 0.577 0.643 5 7870860 missense variant A/G snp 0.47 0.46 60
rs861539 0.561 0.464 14 103699416 missense variant G/A snp 0.29 0.29 59
rs9939609
FTO
0.580 0.607 16 53786615 intron variant T/A snp 0.42 58
rs1800795 0.580 0.607 7 22727026 intron variant C/G snp 0.68 58