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: rs1463038513
rs1463038513
APC
36 0.658 0.440 5 112839511 frameshift variant TAAA/- delins 0.020 1.000 2 1998 2007
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 0.020 1.000 2 1998 2007
dbSNP: rs1801166
rs1801166
APC
17 0.732 0.200 5 112839543 missense variant G/C snv 4.4E-03 5.6E-03 0.020 1.000 2 2003 2009
dbSNP: rs777980327
rs777980327
APC
21 0.716 0.280 5 112837567 missense variant A/T snv 4.0E-06 7.0E-06 0.020 1.000 2 2010 2013
dbSNP: rs137854573
rs137854573
APC
10 0.807 0.120 5 112828889 stop gained C/T snv 0.010 1.000 1 2018 2018
dbSNP: rs137854574
rs137854574
APC
4 0.925 0.120 5 112828919 stop gained C/T snv 0.010 1.000 1 2018 2018
dbSNP: rs2229992
rs2229992
APC
6 0.827 0.200 5 112827157 stop gained T/C;G snv 0.58 0.47 0.010 1.000 1 2011 2011