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rs121913413

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121913413(C;T)
Make rs121913413(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position41224634
GeneCTNNB1
is asnp
is mentioned by
dbSNPrs121913413
ebirs121913413
HLIrs121913413
Exacrs121913413
Varsomers121913413
Maprs121913413
PheGenIrs121913413
hapmaprs121913413
1000 genomesrs121913413
hgdprs121913413
ensemblrs121913413
gopubmedrs121913413
geneviewrs121913413
scholarrs121913413
googlers121913413
pharmgkbrs121913413
gwascentralrs121913413
openSNPrs121913413
23andMers121913413
23andMe allrs121913413
SNP Nexus

SNPshotrs121913413
SNPdbers121913413
MSV3drs121913413
GWAS Ctlgrs121913413
Max Magnitude0
OMIM116806
Desc
Variant0011
Relatedalso
ClinVar
Risk rs121913413(T;T)
Alt rs121913413(T;T)
Reference rs121913413(C;C)
Significance Pathogenic
Disease Pilomatrixoma
Variation info
Gene CTNNB1
CLNDBN Pilomatrixoma
Reversed 0
HGVS NC_000003.11:g.41266125C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000019152.4,