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rs121913409

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121913409(C;T)
Make rs121913409(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position41224646
GeneCTNNB1
is asnp
is mentioned by
dbSNPrs121913409
ebirs121913409
HLIrs121913409
Exacrs121913409
Varsomers121913409
Maprs121913409
PheGenIrs121913409
hapmaprs121913409
1000 genomesrs121913409
hgdprs121913409
ensemblrs121913409
gopubmedrs121913409
geneviewrs121913409
scholarrs121913409
googlers121913409
pharmgkbrs121913409
gwascentralrs121913409
openSNPrs121913409
23andMers121913409
23andMe allrs121913409
SNP Nexus

SNPshotrs121913409
SNPdbers121913409
MSV3drs121913409
GWAS Ctlgrs121913409
Max Magnitude0
OMIM116806
Desc
Variant0013
Relatedalso
ClinVar
Risk rs121913409(A,G,T;A,G,T)
Alt rs121913409(A,G,T;A,G,T)
Reference rs121913409(C;C)
Significance Pathogenic
Disease Hepatocellular carcinoma
Variation info
Gene CTNNB1
CLNDBN Hepatocellular carcinoma
Reversed 0
HGVS NC_000003.11:g.41266137C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000019153.4,