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rs28931588

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs28931588(G;T)
Make rs28931588(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position41224606
GeneCTNNB1
is asnp
is mentioned by
dbSNPrs28931588
ebirs28931588
HLIrs28931588
Exacrs28931588
Varsomers28931588
Maprs28931588
PheGenIrs28931588
hapmaprs28931588
1000 genomesrs28931588
hgdprs28931588
ensemblrs28931588
gopubmedrs28931588
geneviewrs28931588
scholarrs28931588
googlers28931588
pharmgkbrs28931588
gwascentralrs28931588
openSNPrs28931588
23andMers28931588
23andMe allrs28931588
SNP Nexus

SNPshotrs28931588
SNPdbers28931588
MSV3drs28931588
GWAS Ctlgrs28931588
Max Magnitude0
NOTE: the OMIM entry cited below refers to a somatic mutation, not a germline SNP
OMIM116806
DescHEPATOBLASTOMA, SOMATIC
Variant0004
Relatedalso
OMIM116806
DescPILOMATRICOMA, SOMATIC
Variant0016
Relatedalso
Neighborrs28931589
Distance7


ClinVar
Risk rs28931588(A,C,T;A,C,T)
Alt rs28931588(A,C,T;A,C,T)
Reference rs28931588(G;G)
Significance Pathogenic
Disease Hepatoblastoma Pilomatrixoma
Variation info
Gene CTNNB1
CLNDBN Hepatoblastoma Pilomatrixoma
Reversed 0
HGVS NC_000003.11:g.41266097G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000019144.3, RCV000128842.5,



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