Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs1799883 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 36
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
rs1801198 0.677 0.400 22 30615623 missense variant G/A;C snv 5.6E-05; 0.57 26
rs112735431 0.683 0.320 17 80385145 missense variant G/A;C snv 2.6E-04; 8.0E-06 24
rs4291
ACE
0.724 0.400 17 63476833 upstream gene variant T/A;C snv 20
rs5985 0.724 0.280 6 6318562 missense variant C/A;T snv 0.20; 2.4E-05 20
rs387906592 0.752 0.280 10 88941309 missense variant C/T snv 14
rs752596535 0.752 0.200 19 11105407 stop gained C/A;G;T snv 1.6E-05 14
rs28357984
ND2 ; COX1
0.851 0.160 MT 5178 missense variant C/A snv 6
rs3783613 0.851 0.200 1 100731231 missense variant G/A;C snv 4.0E-06; 9.9E-03 6
rs774229224
PLG
0.882 0.160 6 160706454 missense variant C/A;G snv 4.0E-06; 4.0E-06 6
rs9923231 0.851 0.200 16 31096368 upstream gene variant C/A;G;T snv 6
rs2968915 1.000 0.040 X 40580182 intron variant G/A snv 3
rs397514624 0.925 13 110187254 missense variant G/A;C;T snv 1.6E-05; 4.0E-06 3
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1411224107 0.882 0.160 7 101128439 missense variant C/T snv 7.0E-06 4
rs1022113606 0.732 0.280 4 24800161 missense variant G/C snv 1.6E-04 2.1E-05 17
rs544456198 0.790 0.120 19 11116930 missense variant G/T snv 8.0E-06 2.8E-05 9
rs371237692
REN
0.925 0.120 1 204159515 synonymous variant A/G snv 8.0E-06 3.5E-05 5
rs563985037 3 39107505 missense variant C/T snv 4.2E-05 1
rs144467873 0.776 0.120 2 21006289 missense variant G/A snv 1.7E-04 6.3E-05 9