Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 35
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 35
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 30
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 26
rs10401969 0.776 0.240 19 19296909 intron variant T/C snv 0.10 22
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 21
rs7412 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 20
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 18
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 18
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 18
rs4506565 0.790 0.280 10 112996282 intron variant A/G;T snv 18
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 17
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 17
rs1800961 0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02 17
rs855791 0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 17
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 16
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 16
rs174537 0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 14
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 13
rs11066280 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 13
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 12
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 11