Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
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
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
rs2237892 0.790 0.320 11 2818521 intron variant C/T snv 9.2E-02 16
rs5015480 0.851 0.120 10 92705802 downstream gene variant C/T snv 0.42 9