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 73
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 43
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 38
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 36
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 34
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 31
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 29
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 28
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 27
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 25
rs780093 0.763 0.240 2 27519736 intron variant T/C snv 0.68 25
rs174547 0.742 0.240 11 61803311 intron variant T/C snv 0.28 23
rs7412 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 22
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 21
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 20
rs261332 0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 20
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 19
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 17
rs12740374 0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 14
rs6025
F5
0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 14
rs11556924 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 14
rs28601761 1.000 0.040 8 125487789 intron variant C/G snv 0.37 13
rs603424 1.000 0.080 10 100315722 intron variant G/A snv 0.34 13
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 13
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 12