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
rs397507444 0.457 0.714 1 11794407 missense variant T/G snp 169
rs25487 0.485 0.679 19 43551574 missense variant T/C snp 0.68 0.72 119
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
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
rs121913529 0.559 0.393 12 25245350 missense variant C/A,G,T snp 4.0E-06 70
rs1042522 0.563 0.643 17 7676154 stop gained G/C,T snp 0.67 0.62 56
rs1229984 0.622 0.393 4 99318162 missense variant T/C,G snp 0.90 0.94 50
rs121912651 0.618 0.464 17 7674221 missense variant G/A,C snp 4.0E-06 41
rs1045485 0.652 0.393 2 201284866 missense variant G/A,C,T snp 4.0E-06; 9.0E-02 3.2E-05; 9.8E-02 26
rs759728549 0.679 0.214 17 7676223 stop lost T/C snp 8.0E-06 26
rs1799939
RET
0.685 0.250 10 43114671 missense variant G/A,C snp 0.21 0.16 18
rs486907 0.715 0.286 1 182585422 missense variant C/T snp 0.31 0.30 16
rs2066827 0.707 0.250 12 12718165 missense variant T/A,C,G snp 1.6E-04; 1.6E-05; 0.26 0.36 15
rs3218536 0.769 0.179 7 152648922 missense variant C/G,T snp 4.0E-06; 6.4E-02 4.9E-02 9
rs74315364 0.784 0.143 1 182586014 stop gained C/A snp 3.6E-03; 4.0E-06 3.1E-03 8
rs121913527 0.846 0.107 12 25225628 missense variant C/A,G,T snp 6
rs189772026 0.923 0.107 4 152347046 missense variant C/T snp 8.0E-05 3