Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs1799750 0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs5186 0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs8192678 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 28
rs3025058 0.658 0.600 11 102845217 upstream gene variant -/C;G ins 2.8E-04 26
rs182052 0.701 0.440 3 186842993 intron variant G/A snv 0.38 19
rs2266788 0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93 19
rs1183194405
F2
0.716 0.440 11 46719773 missense variant G/A;T snv 4.5E-06; 4.5E-06 19
rs4244285 0.695 0.360 10 94781859 synonymous variant G/A;C snv 0.18 18
rs281865545 0.695 0.360 17 64377836 missense variant C/G;T snv 18
rs3742264 0.742 0.400 13 46073959 missense variant C/T snv 0.31 0.35 17
rs2043556 0.716 0.440 10 51299646 non coding transcript exon variant T/C snv 0.25 0.24 17
rs1187513719 0.851 0.200 10 94780595 missense variant A/G snv 4.0E-06 4
rs1387786689
LPA
1.000 0.080 6 160646235 missense variant G/C snv 1
rs16863352 1.000 0.080 3 151386249 intron variant A/G snv 6.0E-02 1