Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs575231506 0.925 0.160 4 2894667 missense variant C/A;T snv 4.1E-06; 4.1E-06 2
rs747418061
APC
0.807 0.200 5 112828920 missense variant G/A snv 3.2E-05 7.0E-06 10
rs1371086615
APC
0.851 0.120 5 112828890 missense variant G/A snv 4.0E-06 7.0E-06 4
rs765557332
APC
0.851 0.120 5 112835075 missense variant G/A snv 7.0E-06 4
rs878853423
APC
0.851 0.120 5 112837663 missense variant G/A snv 4
rs1431515214
APC
0.925 0.080 5 112839790 missense variant G/A snv 4.0E-06 2
rs13306190 0.807 0.320 2 21032408 missense variant G/A;C;T snv 1.7E-04; 8.0E-06 7
rs777919630
CBS
0.623 0.680 21 43062358 missense variant G/A;T snv 8.0E-06; 4.0E-06 40
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs1799963
F2
0.695 0.400 11 46739505 3 prime UTR variant G/A snv 9.6E-03 25
rs1183194405
F2
0.716 0.440 11 46719773 missense variant G/A;T snv 4.5E-06; 4.5E-06 19
rs552953108
F2
0.724 0.200 11 46729529 missense variant G/A snv 1.6E-05 4.2E-05 16
rs780225764
F2
1.000 0.080 11 46726797 missense variant A/G snv 4.0E-06 2
rs779829591
F3
0.827 0.320 1 94532395 missense variant G/A snv 4.0E-06 5
rs3789683
F3
0.925 0.200 1 94530506 missense variant C/T snv 6.5E-03 1.0E-02 3
rs751377893
F5
0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 65
rs6025
F5
0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 43
rs1312546120
F5
0.807 0.160 1 169541191 missense variant T/C snv 4.0E-06 7
rs749785846
FGB
0.925 0.160 4 154568469 synonymous variant C/T snv 4.0E-06 2
rs2066865
FGG
0.807 0.240 4 154604124 downstream gene variant G/A snv 0.26 10
rs144246695 0.851 0.160 4 83310887 missense variant G/A snv 8.0E-06 4
rs911028477 1.000 0.080 16 27362773 missense variant G/A snv 2
rs77375493 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs5918 0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13 26