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
10 0.649 0.440 5 112839514 missense variant T/A snv 8.0E-06; 2.0E-03 1.2E-03 0.800 0.861 5 1997 2017
dbSNP: rs62619935
rs62619935
APC
7 0.807 0.120 5 112792446 stop gained C/G;T snv 4.0E-06 0.710 1.000 0 2012 2012
dbSNP: rs755229494
rs755229494
APC
10 0.776 0.080 5 112761654 intron variant A/G snv 9.6E-04 0.700 1.000 1 2019 2019
dbSNP: rs121913224
rs121913224
APC
13 0.742 0.200 5 112839515 frameshift variant AAAGA/- delins 0.700 0
dbSNP: rs121913327
rs121913327
APC
3 0.925 0.120 5 112839606 stop gained C/G;T snv 0.700 0
dbSNP: rs137854573
rs137854573
APC
8 0.807 0.120 5 112828889 stop gained C/T snv 0.700 0
dbSNP: rs137854575
rs137854575
APC
9 0.807 0.120 5 112838399 stop gained C/A;G;T snv 4.7E-04 0.700 0
dbSNP: rs1400295986
rs1400295986
APC
2 0.925 0.080 5 112838233 missense variant T/C snv 0.700 0
dbSNP: rs145945630
rs145945630
APC
7 0.827 0.120 5 112754960 stop gained C/T snv 2.4E-05 0.700 0
dbSNP: rs1554085355
rs1554085355
APC
5 0.851 0.120 5 112839461 stop gained T/A snv 0.700 0
dbSNP: rs397515734
rs397515734
APC
7 0.827 0.120 5 112792494 stop gained C/T snv 0.700 0
dbSNP: rs587781392
rs587781392
APC
7 0.827 0.120 5 112780895 stop gained C/G;T snv 0.700 0
dbSNP: rs779998847
rs779998847
APC
1 1.000 0.080 5 112838262 missense variant G/A snv 8.0E-06 0.700 0
dbSNP: rs786201856
rs786201856
APC
8 0.776 0.200 5 112815507 stop gained C/T snv 0.700 0
dbSNP: rs863225311
rs863225311
APC
7 0.827 0.120 5 112819347 splice region variant A/C;G snv 0.700 0
dbSNP: rs876660765
rs876660765
APC
6 0.851 0.120 5 112815594 splice donor variant G/A snv 0.700 0