Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1010 0.807 0.120 2 85581859 3 prime UTR variant T/C;G snv 7
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1042579 0.732 0.240 20 23048087 missense variant G/A;T snv 0.19 16
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs112735431 0.683 0.320 17 80385145 missense variant G/A;C snv 2.6E-04; 8.0E-06 24
rs11556924 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 21
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs12190287 0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv 19
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1333040 0.732 0.280 9 22083405 intron variant C/G;T snv 15
rs14259 0.724 0.360 12 121915890 missense variant A/C;G snv 4.0E-06; 0.32 19
rs1458766475 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs201058276
F7
0.776 0.240 13 113118731 missense variant G/A;C snv 4.8E-05; 4.0E-06 11
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs2292832 0.605 0.640 2 240456086 non coding transcript exon variant T/A;C snv 0.59 46
rs2305948
KDR
0.732 0.400 4 55113391 missense variant C/A;T snv 4.0E-06; 0.11 18
rs3135506 0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 26
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs3900940 0.827 0.040 3 108428881 missense variant T/A;C snv 4.3E-06; 0.24 6
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs4961 0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 27
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223