Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs12979860 0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs9264942 0.763 0.400 6 31306603 intron variant T/C snv 0.34 15
rs10892151 1.000 11 117661016 intron variant C/T snv 9.7E-02 3
rs11881222 0.925 0.080 19 39244283 intron variant A/G snv 0.30 3
rs4657412 1.000 1 165207796 intron variant G/A snv 0.79 1
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs1799864 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs4149056 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 45
rs58542926 0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs763059810 0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs17235409 0.653 0.600 2 218395009 missense variant G/A;C snv 4.9E-02; 4.1E-06 31
rs3745274 0.672 0.480 19 41006936 missense variant G/A;T snv 4.0E-06; 0.27 30
rs8177374 0.672 0.520 11 126292948 missense variant C/T snv 0.12 0.11 22
rs7439366 0.752 0.320 4 69098620 missense variant T/C snv 0.56 0.57 16
rs1126478
LTF
0.763 0.240 3 46459723 missense variant T/C snv 0.41 0.51 11
rs762513613 0.752 0.280 1 161591315 missense variant A/G snv 4.2E-06 7.4E-06 11
rs765502022 0.827 0.240 4 69112695 missense variant T/C snv 1.6E-05 8