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rs28931589

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs28931589(G;T)
Make rs28931589(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position41224613
GeneCTNNB1
is asnp
is mentioned by
dbSNPrs28931589
ebirs28931589
HLIrs28931589
Exacrs28931589
Varsomers28931589
Maprs28931589
PheGenIrs28931589
hapmaprs28931589
1000 genomesrs28931589
hgdprs28931589
ensemblrs28931589
gopubmedrs28931589
geneviewrs28931589
scholarrs28931589
googlers28931589
pharmgkbrs28931589
gwascentralrs28931589
openSNPrs28931589
23andMers28931589
23andMe allrs28931589
SNP Nexus

SNPshotrs28931589
SNPdbers28931589
MSV3drs28931589
GWAS Ctlgrs28931589
Max Magnitude0
NOTE: the OMIM entry cited below refers to a somatic mutation, not a germline SNP
OMIM116806
DescHEPATOBLASTOMA, SOMATIC
Variant0005
Relatedalso
Neighborrs28931588
Distance7
OMIM116806
Desc
Variant0008
Relatedalso


ClinVar
Risk rs28931589(A,T;A,T)
Alt rs28931589(A,T;A,T)
Reference rs28931589(G;G)
Significance Pathogenic
Disease Pilomatrixoma Hepatoblastoma Malignant tumor of prostate
Variation info
Gene CTNNB1
CLNDBN Pilomatrixoma Hepatoblastoma Malignant tumor of prostate
Reversed 0
HGVS NC_000003.11:g.41266104G>A; NC_000003.11:g.41266104G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000019149.4, RCV000019146.4, RCV000149120.1,



[PMID 19635198] [Correlation of genetic polymorphisms of beta-catenin to hepatitis B virus-related hepatocellular carcinoma].