Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 11
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 10
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 9
rs11075990
FTO
0.925 0.120 16 53785981 intron variant A/G snv 0.41 5
rs12970134 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 5
rs17817964
FTO
0.925 0.120 16 53794154 intron variant C/T snv 0.30 5
rs7202116
FTO
0.882 0.120 16 53787703 intron variant A/G snv 0.41 5
rs9368222 1.000 0.080 6 20686765 intron variant C/A;T snv 5
rs2237892 0.790 0.320 11 2818521 intron variant C/T snv 9.2E-02 4
rs2206734 0.882 0.160 6 20694653 intron variant C/T snv 0.20 3
rs7766070 1.000 0.080 6 20686342 intron variant C/A snv 0.25 3
rs9356744 0.882 0.120 6 20685255 intron variant T/C snv 0.42 3
rs9368219 1.000 0.080 6 20674460 intron variant C/T snv 0.19 3