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: rs1801155
rs1801155
APC
31 0.657 0.393 5 112839514 missense variant T/A snp 2.0E-03; 8.0E-06 6.4E-04 0.030 1.000 3 1998 2016
dbSNP: rs459552
rs459552
APC
10 0.756 0.286 5 112841059 missense variant T/A,G snp 0.79 0.81 0.030 1.000 3 2003 2010
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: 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: 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 2016 2016
dbSNP: rs3838646
rs3838646
5 0.821 0.286 Y 18991182 intron variant CCA/C in-del 0.010 1.000 1 2016 2016
dbSNP: rs454886
rs454886
APC
4 0.846 0.214 5 112810420 intron variant A/G snp 0.25 0.010 1.000 1 2008 2008
dbSNP: rs52812045
rs52812045
4 0.846 0.214 Y 18992540 non coding transcript exon variant G/A snp 0.010 1.000 1 2016 2016