Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs1044498 0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 15
rs10887800 0.790 0.280 10 88316086 intron variant A/G;T snv 11
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs13114738 0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1458766475 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 19
rs1799883 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 36
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
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
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
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4376531 0.925 0.120 8 1906652 intron variant C/A;G snv 4
rs4506565 0.790 0.280 10 112996282 intron variant A/G;T snv 22
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs460976 0.851 0.120 21 41463567 downstream gene variant A/G;T snv 7
rs4704221 0.851 0.120 5 75463358 intron variant T/A;C snv 16