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rs11954856

From SNPedia

Orientationplus
Stabilizedplus
Make rs11954856(G;G)
Make rs11954856(G;T)
Make rs11954856(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position112751630
GeneAPC
is asnp
is mentioned by
dbSNPrs11954856
ebirs11954856
HLIrs11954856
Exacrs11954856
Varsomers11954856
Maprs11954856
PheGenIrs11954856
hapmaprs11954856
1000 genomesrs11954856
hgdprs11954856
ensemblrs11954856
gopubmedrs11954856
geneviewrs11954856
scholarrs11954856
googlers11954856
pharmgkbrs11954856
gwascentralrs11954856
openSNPrs11954856
23andMers11954856
23andMe allrs11954856
SNP Nexus

SNPshotrs11954856
SNPdbers11954856
MSV3drs11954856
GWAS Ctlgrs11954856
GMAF0.3898
Max Magnitude
? (G;G) (G;T) (T;T) 28
[PMID 24078348OA-icon.png] An Analysis of Polymorphisms Within the Wnt Signaling Pathway in Relation to Ovarian Cancer Risk in a Polish Population


[PMID 18708403OA-icon.png] Association of genetic variation in genes implicated in the beta-catenin destruction complex with risk of breast cancer.


ClinVar
Risk rs11954856(G;G)
Alt rs11954856(G;G)
Reference rs11954856(T;T)
Significance Other
Disease Familial colorectal cancer
Variation info
Gene APC
CLNDBN Familial colorectal cancer
Reversed 0
HGVS NC_000005.9:g.112087327T>G
CLNSRC ClinVar
CLNACC RCV000073790.1,