Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs55770810
rs55770810
10 0.763 0.280 17 43063931 missense variant G/A;T snv 2.4E-05; 8.0E-06 0.800 0
dbSNP: rs28897672
rs28897672
16 0.732 0.280 17 43106487 missense variant A/C;G;T snv 3.2E-05 0.730 1.000 3 2006 2010
dbSNP: rs2072590
rs2072590
4 0.851 0.120 2 176177905 non coding transcript exon variant A/C;T snv 0.720 1.000 4 2010 2017
dbSNP: rs3814113
rs3814113
5 0.827 0.200 9 16915023 upstream gene variant T/C snv 0.41 0.720 1.000 4 2009 2013
dbSNP: rs1801155
rs1801155
APC
42 0.649 0.440 5 112839514 missense variant T/A snv 8.0E-06; 2.0E-03 1.2E-03 0.720 1.000 2 1997 1998
dbSNP: rs10088218
rs10088218
4 0.851 0.120 8 128531703 intron variant G/A snv 0.13 0.710 1.000 3 2010 2013
dbSNP: rs121913279
rs121913279
101 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 0.710 1.000 2 2004 2016
dbSNP: rs2363956
rs2363956
8 0.776 0.160 19 17283315 missense variant T/G snv 0.48 0.50 0.710 1.000 2 2010 2012
dbSNP: rs2665390
rs2665390
8 0.776 0.160 3 156679960 intron variant C/T snv 0.92 0.710 1.000 2 2010 2012
dbSNP: rs17879961
rs17879961
53 0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 0.710 1.000 1 2006 2006
dbSNP: rs28933370
rs28933370
3 0.882 0.120 17 39725125 missense variant A/G snv 7.0E-06 0.700 1.000 5 2004 2013
dbSNP: rs121913403
rs121913403
23 0.683 0.240 3 41224622 missense variant C/A;G;T snv 0.700 1.000 3 2008 2013
dbSNP: rs137852691
rs137852691
2 0.925 0.120 11 132657203 missense variant G/A;C snv 8.0E-06 0.700 1.000 3 2008 2013
dbSNP: rs9303542
rs9303542
3 0.882 0.120 17 48334138 intron variant A/G snv 0.34 0.700 1.000 2 2010 2013
dbSNP: rs10756819
rs10756819
1 1.000 0.120 9 16858086 intron variant G/A;C;T snv 0.700 1.000 1 2009 2009
dbSNP: rs10810666
rs10810666
1 1.000 0.120 9 16911668 intergenic variant C/T snv 0.14 0.700 1.000 1 2009 2009
dbSNP: rs10962656
rs10962656
1 1.000 0.120 9 16877790 intergenic variant G/A snv 0.10 0.700 1.000 1 2009 2009
dbSNP: rs11782652
rs11782652
4 0.851 0.120 8 81741409 intron variant A/G snv 6.6E-02 0.700 1.000 1 2013 2013
dbSNP: rs12379183
rs12379183
1 1.000 0.120 9 16865701 intron variant A/G snv 0.26 0.700 1.000 1 2009 2009
dbSNP: rs12379687
rs12379687
1 1.000 0.120 9 16854369 intron variant G/A;T snv 0.700 1.000 1 2009 2009
dbSNP: rs1243180
rs1243180
7 0.790 0.160 10 21626690 intron variant T/A snv 0.23 0.700 1.000 1 2013 2013
dbSNP: rs12451939
rs12451939
1 1.000 0.120 17 61970281 intron variant A/G snv 2.6E-02 0.700 1.000 1 2011 2011
dbSNP: rs12937080
rs12937080
1 1.000 0.120 17 61852376 intron variant A/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs12938171
rs12938171
1 1.000 0.120 17 61902994 intron variant G/A snv 9.0E-03 0.700 1.000 1 2011 2011
dbSNP: rs1339552
rs1339552
1 1.000 0.120 9 16848792 intron variant C/T snv 0.52 0.700 1.000 1 2009 2009