Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 25
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs2075650 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 15
rs780093 0.763 0.240 2 27519736 intron variant T/C snv 0.68 13
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 12
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 11
rs157580 0.882 0.160 19 44892009 intron variant G/A snv 0.69 11
rs10468017 0.851 0.120 15 58386313 intron variant C/T snv 0.24 10
rs673548 0.925 0.120 2 21014672 intron variant G/A;T snv 10
rs1535 0.752 0.240 11 61830500 intron variant A/G snv 0.31 10
rs174570 0.882 0.200 11 61829740 intron variant C/T snv 0.15 10
rs174547 0.742 0.240 11 61803311 intron variant T/C snv 0.28 10
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10
rs6511720 0.790 0.120 19 11091630 intron variant G/T snv 0.12 10
rs102275 0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 10
rs2068834 0.925 0.120 2 27616672 intron variant T/C snv 0.28 10
rs1532085 0.882 0.080 15 58391167 intron variant A/G;T snv 9
rs174546 0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 9
rs174576 0.851 0.200 11 61836038 intron variant C/A;T snv 9
rs174548 0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 9
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 9
rs1260333 0.882 0.160 2 27525757 downstream gene variant A/G snv 0.58 8
rs17482753 1.000 0.080 8 19975135 regulatory region variant G/T snv 8.8E-02 8
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 8