Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17319721 0.925 0.080 4 76447694 intron variant G/A snv 0.34 5
rs530391015 0.882 0.080 14 104703445 stop gained G/A;C;T snv 4.0E-06 5
rs867394500
ACE
0.851 0.080 17 63477301 missense variant G/T snv 4
rs1567202189 1.000 0.080 16 2111276 inframe insertion -/GTG ins 2
rs367825197 0.925 0.080 7 131509412 stop gained G/A snv 4.0E-06 2
rs538166970
ACE
0.925 0.080 17 63496920 missense variant G/A;C snv 1.6E-05; 4.0E-06 2
rs12704795 1.000 0.080 7 95424695 intron variant T/G snv 0.34 1
rs7456421 0.882 0.120 7 139715976 synonymous variant G/C snv 0.27 0.37 4
rs1553948516 0.925 0.120 4 76181009 frameshift variant -/G delins 3
rs7222094 0.882 0.120 17 45290287 intron variant T/C snv 0.54 3
rs886039813 0.827 0.160 X 13756600 frameshift variant C/- delins 8
rs281874657 0.925 0.160 X 108586717 stop gained C/T snv 3
rs1382048442 0.925 0.160 10 99797141 missense variant T/C snv 4.0E-06 2
rs138207257 0.925 0.160 10 97611535 missense variant G/A;T snv 2.0E-05; 1.1E-04 2
rs202047589 0.925 0.160 10 97599780 missense variant C/T snv 4.4E-05 7.0E-05 2
rs188942711 0.763 0.200 2 227253336 missense variant G/A;T snv 2.8E-05; 4.0E-06 9
rs118203478 0.882 0.200 9 132911492 frameshift variant -/A;AA delins 5
rs61747728 0.701 0.240 1 179557079 missense variant C/T snv 3.0E-02 2.8E-02 20
rs34557412 0.763 0.240 17 16948873 missense variant A/G snv 3.5E-03 3.9E-03 15
rs12026 0.827 0.240 7 95411704 missense variant G/C snv 0.27 0.27 6
rs771454167 0.827 0.240 12 88062772 frameshift variant C/- del 4.7E-05; 5.2E-06 2.1E-05 6
rs1555487316 0.882 0.240 16 20348247 missense variant A/C snv 5
rs137852832 0.716 0.280 12 88077263 stop gained C/A snv 9.5E-05 6.3E-05 17
rs137852834 0.763 0.280 12 88083936 stop gained T/A snv 5.5E-05 9.1E-05 13
rs121918079
TTR
0.790 0.280 18 31595143 missense variant T/C snv 10