Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs53576 0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs2254298 0.701 0.200 3 8760542 intron variant G/A snv 0.16 23
rs17810023 0.925 0.080 6 80443056 non coding transcript exon variant C/T snv 1.7E-02 2
rs200889048 0.882 0.120 3 74928276 intergenic variant C/- del 3
rs1630623 0.882 0.120 9 72725323 intron variant A/G snv 0.29 3
rs145763646 0.925 0.080 3 66173478 intron variant G/A snv 0.13 2
rs372794914 0.925 0.080 18 60372319 missense variant T/C snv 6.0E-05 2.8E-05 2
rs752031670 0.925 0.080 18 60371752 missense variant T/C snv 2.4E-05 1.4E-05 2
rs12970134 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 13
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 21
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 28
rs2296972 0.925 0.080 13 46854336 intron variant A/C snv 0.70 4
rs6006893 0.925 0.080 22 44858015 intron variant C/T snv 0.15 2
rs726170 0.925 0.080 22 44855931 intron variant C/T snv 0.15 2
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs746682028 0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs76087671 0.925 0.080 20 24330541 intergenic variant C/A;G;T snv 2
rs10198175 0.925 0.080 2 20934123 intergenic variant A/G snv 0.93 3
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1950038 0.925 0.080 2 183579642 regulatory region variant T/C snv 0.71 2
rs73057489 0.925 0.080 12 17370820 regulatory region variant A/C snv 3.9E-02 2
rs7904579 0.925 0.080 10 17089754 intron variant G/A;C snv 2
rs12490016 0.882 0.120 3 157121142 intron variant G/C snv 4.6E-02 3