Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3751143 0.742 0.480 12 121184501 missense variant A/C;G snv 0.19; 4.0E-06 12
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs10741657 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs147377392 0.763 0.120 20 23048144 missense variant A/G snv 1.0E-04 2.8E-04 11
rs2383207 0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs872129 0.925 0.080 1 203200263 intergenic variant A/G snv 0.19 2
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 14
rs752596535 0.752 0.200 19 11105407 stop gained C/A;G;T snv 1.6E-05 14
rs11053646 0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13 18
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs1764391 0.790 0.160 1 34795168 missense variant C/G;T snv 0.30 7
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs17057255 0.925 0.080 8 27503724 missense variant C/T snv 1.3E-02 3.4E-02 2
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs6025
F5
0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 43