Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 35
rs1800961 0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02 17
rs2074356 0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 9
rs2925979 1.000 0.080 16 81501185 intron variant T/A;C snv 9
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 7
rs2972143 1.000 0.080 2 226251649 intergenic variant A/G snv 0.67 4
rs7185735
FTO
0.925 0.120 16 53788739 intron variant A/G;T snv 4
rs10734252 1.000 0.080 11 17383292 non coding transcript exon variant G/A snv 0.71 3