Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1232898090 0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1440763451 0.882 0.080 3 12416849 missense variant A/G snv 4.0E-06 4
rs1458766475 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
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
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs2295490 0.724 0.320 20 388261 missense variant A/G;T snv 0.18; 4.0E-06 16
rs2536512 0.752 0.280 4 24799693 missense variant G/A;T snv 0.55 14
rs3135506 0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 26
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs774887459 0.882 0.080 22 40405776 missense variant G/A snv 4.0E-06 4
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs755725121 0.882 0.080 1 9716029 missense variant G/A snv 2.1E-05 7.0E-06 4
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1298417395 0.882 0.080 1 176206716 missense variant C/T snv 1.4E-05 4
rs1022113606 0.732 0.280 4 24800161 missense variant G/C snv 1.6E-04 2.1E-05 17
rs773297988 0.882 0.080 3 138698965 missense variant T/C snv 4.0E-06 3.5E-05 4
rs375752214 0.708 0.400 7 150998541 missense variant C/T snv 4.1E-06 4.2E-05 22