Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 21
rs5744680 0.851 0.120 5 75584065 intron variant G/A snv 0.55 18
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 15
rs715 1.000 0.040 2 210678331 3 prime UTR variant T/C snv 0.28 13
rs1126930 12 49005349 missense variant G/C snv 2.1E-02 2.1E-02 5
rs36023504 4 38697303 3 prime UTR variant C/G;T snv 0.24 0.24 3
rs7185966 16 3972702 intron variant G/A snv 0.26 3