Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34536443 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 25
rs2187668 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 20
rs7517847 0.689 0.600 1 67215986 intron variant T/G snv 0.37 19
rs2076530 0.724 0.640 6 32396039 missense variant T/C snv 0.42 0.40 17
rs3117582 0.716 0.440 6 31652743 intron variant T/G snv 7.1E-02 14
rs179008 0.763 0.360 X 12885540 missense variant A/C;T snv 0.18 0.18 14
rs2516049 0.742 0.400 6 32602623 intergenic variant T/C snv 0.27 12
rs3811381
CR1
0.763 0.240 1 207616743 missense variant C/A;G snv 8.0E-06; 0.24 11
rs9461776 0.763 0.240 6 32607958 intergenic variant A/G snv 8.8E-02 11
rs2247056 0.882 0.160 6 31297713 intron variant T/C snv 0.80 11
rs9271770 0.776 0.120 6 32626471 upstream gene variant G/A snv 0.76 10
rs1800076 0.763 0.200 7 117509093 missense variant G/A;T snv 1.5E-02; 8.0E-06 10
rs10877012 0.763 0.280 12 57768302 intron variant G/C;T snv 10
rs1480380 0.763 0.360 6 32945469 intron variant C/T snv 0.11 10
rs477515 0.790 0.400 6 32601914 intergenic variant G/A snv 0.27 10
rs11465804 0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 10
rs9257809 0.790 0.320 6 29388554 intron variant A/G snv 5.8E-02 10
rs389884 0.776 0.440 6 31973120 non coding transcript exon variant A/G snv 7.1E-02 10
rs694739 0.763 0.320 11 64329761 upstream gene variant A/G snv 0.28 9
rs3177928 0.882 0.120 6 32444658 3 prime UTR variant G/A snv 0.13 8
rs2075800 0.776 0.440 6 31810169 missense variant C/T snv 0.32 0.25 8
rs3817963 0.776 0.360 6 32400310 intron variant T/C snv 0.25 8
rs7194 0.827 0.280 6 32444703 3 prime UTR variant G/A snv 0.61 7
rs9298814 0.790 0.160 9 21227623 missense variant A/C;G snv 0.12; 8.8E-06 7
rs7667298
KDR
0.827 0.120 4 55125564 5 prime UTR variant T/C snv 0.48 7