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: rs1761667
rs1761667
12 0.752 0.320 7 80615623 intron variant G/A snv 0.49 0.010 1.000 1 2018 2018
dbSNP: rs1984112
rs1984112
8 0.807 0.280 7 80613604 intron variant A/G snv 0.33 0.010 1.000 1 2018 2018
dbSNP: rs876658325
rs876658325
APC
3 0.925 0.120 5 112775687 stop gained C/T snv 0.010 1.000 1 2012 2012
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 0.010 1.000 1 2012 2012
dbSNP: rs1801166
rs1801166
APC
17 0.732 0.200 5 112839543 missense variant G/C snv 4.4E-03 5.6E-03 0.010 1.000 1 2009 2009
dbSNP: rs753314927
rs753314927
APC
3 0.882 0.200 5 112838644 missense variant A/G;T snv 0.010 1.000 1 2008 2008
dbSNP: rs1463038513
rs1463038513
APC
36 0.658 0.440 5 112839511 frameshift variant TAAA/- delins 0.010 1.000 1 2012 2012