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rs876658941

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876658941(G;T)
Make rs876658941(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position112766410
GeneAPC
is asnp
is mentioned by
dbSNPrs876658941
dbSNP (classic)rs876658941
ClinGenrs876658941
ebirs876658941
HLIrs876658941
Exacrs876658941
Gnomadrs876658941
Varsomers876658941
LitVarrs876658941
Maprs876658941
PheGenIrs876658941
Biobankrs876658941
1000 genomesrs876658941
hgdprs876658941
ensemblrs876658941
geneviewrs876658941
scholarrs876658941
googlers876658941
pharmgkbrs876658941
gwascentralrs876658941
openSNPrs876658941
23andMers876658941
SNPshotrs876658941
SNPdbers876658941
MSV3drs876658941
GWAS Ctlgrs876658941
Max Magnitude0
ClinVar
Risk rs876658941(T;T)
Alt rs876658941(T;T)
Reference Rs876658941(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided Familial adenomatous polyposis 1
Variation info
Gene APC
CLNDBN Hereditary cancer-predisposing syndrome not provided Familial adenomatous polyposis 1
Reversed 0
HGVS NC_000005.9:g.112102107G>T
CLNSRC
CLNACC RCV000215333.1, RCV000254875.2, RCV000459175.1,