Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs6025
F5
0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 43
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35
rs11591147 0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 28
rs1764391 0.790 0.160 1 34795168 missense variant C/G;T snv 0.30 7
rs567798234 0.851 0.120 1 109625326 missense variant C/T snv 4.1E-06 7.0E-06 5
rs872129 0.925 0.080 1 203200263 intergenic variant A/G snv 0.19 2
rs3917643
F3
1.000 0.040 1 94536311 intron variant T/C snv 3.9E-02 1
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs5742904 0.689 0.280 2 21006288 missense variant C/A;T snv 2.8E-04 7.3E-04 22
rs4988235 0.752 0.400 2 135851076 intron variant G/A;C snv 19
rs6742078 0.807 0.240 2 233763993 intron variant G/T snv 0.36 13
rs12713559 0.776 0.120 2 21006196 missense variant G/A snv 3.4E-04 5.0E-04 10
rs6749704 0.827 0.240 2 227813126 intron variant T/C snv 0.24 5
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs1799895 0.683 0.360 4 24800212 missense variant C/G snv 2.3E-02 1.2E-02 26
rs1022113606 0.732 0.280 4 24800161 missense variant G/C snv 1.6E-04 2.1E-05 17
rs6834314 0.807 0.160 4 87292656 intergenic variant A/G snv 0.24 10
rs1800888 0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 23
rs33972313 0.790 0.160 5 139379813 missense variant C/A;G;T snv 4.0E-06; 2.7E-02 8