Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12567209 0.807 0.080 1 162066689 upstream gene variant G/A snv 8.6E-02 6
rs2306235 0.827 0.040 1 150150942 missense variant C/G;T snv 1.1E-02; 1.6E-05 4.4E-03 6
rs37369 0.807 0.120 5 35037010 missense variant C/T snv 0.21 0.25 9
rs8259
BSG
0.776 0.200 19 582927 3 prime UTR variant T/A snv 0.39 9
rs911119 0.807 0.120 20 23632100 non coding transcript exon variant C/G;T snv 9
rs1320702652 0.752 0.160 15 43824536 missense variant G/A snv 4.0E-06 11
rs1799998 0.742 0.200 8 142918184 upstream gene variant A/G;T snv 0.38 14
rs10757274 0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs2383207 0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs1799895 0.683 0.360 4 24800212 missense variant C/G snv 2.3E-02 1.2E-02 26
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35
rs5370 0.630 0.520 6 12296022 missense variant G/T snv 0.23 0.21 37
rs5186 0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs4149056 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 45
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs2070744 0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106