Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7895833 0.742 0.440 10 67863299 upstream gene variant G/A;C snv 12
rs897876 0.882 0.040 2 65564447 intron variant C/T snv 0.30 4
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs72653706 0.695 0.480 16 16163078 stop gained G/A snv 1.4E-03 1.2E-03 32
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs142677199
ACE
0.882 0.040 17 63479897 missense variant G/A;T snv 3.2E-05 4
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs761401927
ACE
0.882 0.040 17 63488704 missense variant G/A snv 9.1E-05 4
rs4961 0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 27
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs185847354 0.763 0.160 3 186854460 missense variant T/C snv 3.1E-04 7.0E-05 11
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs6903956 0.763 0.160 6 11774350 intron variant A/G snv 0.65 10
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs762079672
AGT
0.882 0.040 1 230710211 missense variant C/T snv 4.0E-06 4
rs5182 0.742 0.160 3 148741608 synonymous variant C/T snv 0.49 0.41 16
rs5186 0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs553350297 0.882 0.040 3 148741588 missense variant G/A snv 1.2E-05 2.1E-05 4
rs1800588 0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 16