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: rs72541816
rs72541816
APC
5 0.821 0.107 5 112843456 missense variant C/G snp 2.9E-03 3.4E-03 0.720 0.500 2 1997 2002
dbSNP: rs139196838
rs139196838
APC
5 0.821 0.107 5 112767263 missense variant C/A,T snp 4.0E-06; 3.9E-04 4.5E-04 0.700 1 1995 1995
dbSNP: rs371113837
rs371113837
APC
5 0.821 0.107 5 112839469 missense variant C/T snp 8.8E-05 1.3E-04 0.700 1 1993 1993
dbSNP: rs137854567
rs137854567
APC
5 0.821 0.107 5 112819272 stop gained C/A,T snp 4.0E-06; 6.7E-04 4.1E-04 0.700 0
dbSNP: rs863225349
rs863225349
APC
6 0.821 0.107 5 112839531 missense variant A/G snp 0.700 0
dbSNP: rs876658156
rs876658156
APC
5 0.821 0.107 5 112844109 missense variant C/T snp 0.700 0
dbSNP: rs1801155
rs1801155
APC
31 0.657 0.393 5 112839514 missense variant T/A snp 2.0E-03; 8.0E-06 6.4E-04 0.050 1.000 5 1998 2016
dbSNP: rs459552
rs459552
APC
10 0.756 0.286 5 112841059 missense variant T/A,G snp 0.79 0.81 0.050 1.000 5 2002 2010
dbSNP: rs1801166
rs1801166
APC
12 0.756 0.179 5 112839543 missense variant G/C snp 4.4E-03 4.3E-03 0.040 1.000 4 2004 2016
dbSNP: rs2266780
rs2266780
4 0.923 0.143 1 171114102 missense variant A/G snp 0.15 0.16 0.030 1.000 3 2005 2008
dbSNP: rs34612342
rs34612342
20 0.692 0.179 1 45332803 missense variant T/C snp 1.5E-03 1.6E-03 0.020 1.000 2 2003 2007
dbSNP: rs36053993
rs36053993
20 0.699 0.214 1 45331556 missense variant C/T snp 3.0E-03 3.3E-03 0.020 1.000 2 2003 2007
dbSNP: rs565453
rs565453
3 0.878 0.143 5 112849696 intron variant A/C,G snp 0.64 0.020 1.000 2 2010 2013
dbSNP: rs1058818
rs1058818
2 0.923 0.179 Y 18991654 intron variant C/T snp 0.010 1.000 1 2016 2016
dbSNP: rs1058881
rs1058881
2 0.923 0.179 Y 18991085 intron variant C/T snp 0.010 1.000 1 2016 2016
dbSNP: rs113488022
rs113488022
267 0.407 0.786 7 140753336 missense variant snp 4.0E-06 0.010 < 0.001 1 2007 2007
dbSNP: rs11541794
rs11541794
TTR
3 0.878 0.179 18 31593004 missense variant A/G snp 0.010 1.000 1 2012 2012
dbSNP: rs121913530
rs121913530
39 0.615 0.321 12 25245351 missense variant C/A,G,T snp 0.010 1.000 1 2014 2014
dbSNP: rs150973053
rs150973053
APC
4 0.846 0.179 5 112767356 missense variant A/G snp 3.5E-04 9.6E-05 0.010 1.000 1 2008 2008
dbSNP: rs1816769
rs1816769
APC
1 1.000 0.107 5 112774082 intron variant G/C snp 0.53 0.010 1.000 1 2013 2013
dbSNP: rs28933979
rs28933979
TTR
9 0.769 0.250 18 31592974 missense variant G/A,C snp 1.0E-04 0.010 1.000 1 2018 2018
dbSNP: rs376961112
rs376961112
GSN
4 0.846 0.214 9 121302059 missense variant G/A snp 4.0E-06 3.2E-05 0.010 1.000 1 2012 2012
dbSNP: rs3838646
rs3838646
5 0.821 0.286 Y 18991182 intron variant CCA/C in-del 0.010 1.000 1 2016 2016
dbSNP: rs3846716
rs3846716
APC
1 1.000 0.107 5 112723897 intron variant A/G snp 0.51 0.010 1.000 1 2010 2010
dbSNP: rs41115
rs41115
APC
3 0.878 0.143 5 112840073 synonymous variant G/A snp 0.65 0.59 0.010 1.000 1 2010 2010