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rs121913400

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121913400(A;A)
Make rs121913400(A;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position41224610
GeneCTNNB1
is asnp
is mentioned by
dbSNPrs121913400
ebirs121913400
HLIrs121913400
Exacrs121913400
Varsomers121913400
Maprs121913400
PheGenIrs121913400
hapmaprs121913400
1000 genomesrs121913400
hgdprs121913400
ensemblrs121913400
gopubmedrs121913400
geneviewrs121913400
scholarrs121913400
googlers121913400
pharmgkbrs121913400
gwascentralrs121913400
openSNPrs121913400
23andMers121913400
23andMe allrs121913400
SNP Nexus

SNPshotrs121913400
SNPdbers121913400
MSV3drs121913400
GWAS Ctlgrs121913400
Max Magnitude0
OMIM116806
Desc
Variant0002
Relatedalso
OMIM116806
Desc
Variant0007
Relatedalso
ClinVar
Risk rs121913400(A,G,T;A,G,T)
Alt rs121913400(A,G,T;A,G,T)
Reference rs121913400(C;C)
Significance Pathogenic
Disease Carcinoma of colon Pilomatrixoma Medulloblastoma
Variation info
Gene CTNNB1
CLNDBN Carcinoma of colon Pilomatrixoma Medulloblastoma
Reversed 0
HGVS NC_000003.11:g.41266101C>A; NC_000003.11:g.41266101C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000019138.4, RCV000019139.4, RCV000019147.4, RCV000019148.4,