Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 32
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 28
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 16
rs12970134 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 13
rs2815752 0.925 0.200 1 72346757 intron variant G/A snv 0.62 7