Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2237895 0.790 0.240 11 2835964 intron variant A/C;T snv 10
rs780093 0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs1022113606 0.732 0.280 4 24800161 missense variant G/C snv 1.6E-04 2.1E-05 17
rs1800777 0.724 0.280 16 56983407 missense variant G/A snv 3.7E-02 2.8E-02 17
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs10757274 0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs1129844 0.752 0.320 17 34285875 missense variant G/A;C;T snv 0.16; 1.2E-05 13
rs2016520 0.752 0.320 6 35411001 5 prime UTR variant C/T snv 0.78 16
rs2237892 0.790 0.320 11 2818521 intron variant C/T snv 9.2E-02 16
rs2295490 0.724 0.320 20 388261 missense variant A/G;T snv 0.18; 4.0E-06 16
rs660339 0.695 0.320 11 73978059 missense variant G/A snv 0.41 0.43 24
rs1044498 0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 15
rs11066001 0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 15
rs1799895 0.683 0.360 4 24800212 missense variant C/G snv 2.3E-02 1.2E-02 26
rs505151 0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 18
rs7080536 0.683 0.360 10 113588287 missense variant G/A snv 2.2E-02 2.4E-02 27
rs1800888 0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 23
rs3135506 0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 26
rs375752214 0.708 0.400 7 150998541 missense variant C/T snv 4.1E-06 4.2E-05 22
rs4402960 0.724 0.400 3 185793899 intron variant G/T snv 0.38 21
rs4918 0.763 0.400 3 186620593 missense variant G/A;C snv 0.67 12
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs1799883 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 36
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35
rs58542926 0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42