Have questions? Visit https://www.reddit.com/r/SNPedia

rs121913407

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121913407(C;C)
Make rs121913407(C;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position41224645
GeneCTNNB1
is asnp
is mentioned by
dbSNPrs121913407
ebirs121913407
HLIrs121913407
Exacrs121913407
Varsomers121913407
Maprs121913407
PheGenIrs121913407
hapmaprs121913407
1000 genomesrs121913407
hgdprs121913407
ensemblrs121913407
gopubmedrs121913407
geneviewrs121913407
scholarrs121913407
googlers121913407
pharmgkbrs121913407
gwascentralrs121913407
openSNPrs121913407
23andMers121913407
23andMe allrs121913407
SNP Nexus

SNPshotrs121913407
SNPdbers121913407
MSV3drs121913407
GWAS Ctlgrs121913407
Max Magnitude0
OMIM116806
Desc
Variant0014
Relatedalso
ClinVar
Risk rs121913407(C,G;C,G)
Alt rs121913407(C,G;C,G)
Reference rs121913407(T;T)
Significance Pathogenic
Disease Hepatocellular carcinoma not provided
Variation info
Gene CTNNB1
CLNDBN Hepatocellular carcinoma not provided
Reversed 0
HGVS NC_000003.11:g.41266136T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000019154.4, RCV000087197.2,