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rs121913412

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121913412(A;G)
Make rs121913412(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position41224633
GeneCTNNB1
is asnp
is mentioned by
dbSNPrs121913412
ebirs121913412
HLIrs121913412
Exacrs121913412
Varsomers121913412
Maprs121913412
PheGenIrs121913412
hapmaprs121913412
1000 genomesrs121913412
hgdprs121913412
ensemblrs121913412
gopubmedrs121913412
geneviewrs121913412
scholarrs121913412
googlers121913412
pharmgkbrs121913412
gwascentralrs121913412
openSNPrs121913412
23andMers121913412
23andMe allrs121913412
SNP Nexus

SNPshotrs121913412
SNPdbers121913412
MSV3drs121913412
GWAS Ctlgrs121913412
Max Magnitude0
OMIM116806
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121913412(C,G,T;C,G,T)
Alt rs121913412(C,G,T;C,G,T)
Reference rs121913412(A;A)
Significance Other
Disease Hepatoblastoma Desmoid tumor not provided
Variation info
Gene CTNNB1
CLNDBN Hepatoblastoma Desmoid tumor, somatic not provided
Reversed 0
HGVS NC_000003.11:g.41266124A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000019142.4, RCV000019143.4, RCV000087196.3,