Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs153109 0.623 0.600 16 28507775 intron variant T/C snv 0.43 37
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs4646903 0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18 36
rs10741657 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs174547 0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs1800624 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs368087026 0.637 0.520 21 45530890 missense variant G/A snv 33
rs4950928 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33
rs662799 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs7799039 0.649 0.560 7 128238730 upstream gene variant G/A;C snv 33
rs151344517 0.742 0.320 18 12337505 missense variant C/T snv 31
rs1799889 0.649 0.600 7 101126430 upstream gene variant A/G snv 31
rs780093 0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs12255372 0.667 0.480 10 113049143 intron variant G/A;T snv 28
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 28
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26 27
rs11536889 0.658 0.560 9 117715853 3 prime UTR variant G/C snv 0.11 27
rs599839 0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs2071559
KDR
0.667 0.680 4 55126199 upstream gene variant A/G snv 0.53 26
rs3025058 0.658 0.600 11 102845217 upstream gene variant -/C;G ins 2.8E-04 26
rs4977574 0.695 0.520 9 22098575 intron variant A/G;T snv 26
rs10401969 0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs12785878 0.677 0.520 11 71456403 intron variant G/A;T snv 25
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25