Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1020608562 0.807 0.160 3 46373738 missense variant T/C snv 4.0E-06 9
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
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
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 16
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs17465637 0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 11
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
rs2106261 0.763 0.160 16 73017721 intron variant C/G;T snv 11
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
rs4606 0.752 0.120 1 192812042 3 prime UTR variant C/G;T snv 16
rs4673 0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 32
rs4961 0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 27
rs5351 0.807 0.240 13 77901178 synonymous variant T/C;G snv 0.57 7
rs5882 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs549591993
F7
0.776 0.400 13 113105794 5 prime UTR variant C/A snv 4.0E-04 2.8E-05 12
rs185847354 0.763 0.160 3 186854460 missense variant T/C snv 3.1E-04 7.0E-05 11