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: rs113488022
rs113488022
267 0.407 0.786 7 140753336 missense variant snp 4.0E-06 0.070 1.000 7 2007 2016
dbSNP: rs1042821
rs1042821
11 0.756 0.214 2 47783349 missense variant G/A,C snp 0.18; 8.6E-06 0.19 0.010 1.000 1 2006 2006
dbSNP: rs17655
rs17655
39 0.611 0.500 13 102875652 missense variant G/C snp 0.28 0.30 0.010 1.000 1 2006 2006
dbSNP: rs1799977
rs1799977
20 0.679 0.357 3 37012077 missense variant A/C,G,T snp 0.23 0.23 0.010 1.000 1 2006 2006
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 0.010 < 0.001 1 2000 2000
dbSNP: rs1801166
rs1801166
APC
12 0.756 0.179 5 112839543 missense variant G/C snp 4.4E-03 4.3E-03 0.010 1.000 1 1998 1998
dbSNP: rs3842787
rs3842787
5 0.846 0.107 9 122371228 missense variant C/T snp 5.9E-02 8.5E-02 0.010 < 0.001 1 2004 2004
dbSNP: rs5789
rs5789
4 0.878 0.107 9 122381694 missense variant C/A snp 1.8E-02 1.4E-02 0.010 < 0.001 1 2004 2004
dbSNP: rs8042919
rs8042919
2 0.923 0.107 15 50586433 missense variant G/A,T snp 8.5E-02 7.2E-02 0.010 1.000 1 2008 2008