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
rs4680 0.484 0.821 22 19963748 missense variant G/A snp 0.46 0.45 155
rs4986790 0.465 0.750 9 117713024 missense variant A/G,T snp 6.1E-02; 4.0E-06 6.7E-02 146
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
rs77375493 0.504 0.536 9 5073770 missense variant G/A,T snp 3.5E-04 2.9E-04 106
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
rs9939609
FTO
0.580 0.607 16 53786615 intron variant T/A snp 0.42 74
rs662 0.561 0.607 7 95308134 missense variant T/C snp 0.38 0.41 71
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
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
rs5498 0.570 0.679 19 10285007 missense variant A/G snp 0.44 0.36 53
rs1229984 0.622 0.393 4 99318162 missense variant T/C,G snp 0.90 0.94 50