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
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
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
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 25
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 23
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
rs174547 0.742 0.240 11 61803311 intron variant T/C snv 0.28 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
rs780093 0.763 0.240 2 27519736 intron variant T/C snv 0.68 16
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
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv 14
rs7137828 0.763 0.200 12 111494996 intron variant C/A;T snv 14
rs174537 0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 14
rs28601761 1.000 0.040 8 125487789 intron variant C/G snv 0.37 13
rs11556924 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 13
rs17696736 0.827 0.240 12 112049014 intron variant A/G snv 0.30 12
rs2075650 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 12
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 11