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rs121913396

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121913396(A;G)
Make rs121913396(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position41224607
GeneCTNNB1
is asnp
is mentioned by
dbSNPrs121913396
ebirs121913396
HLIrs121913396
Exacrs121913396
Varsomers121913396
Maprs121913396
PheGenIrs121913396
hapmaprs121913396
1000 genomesrs121913396
hgdprs121913396
ensemblrs121913396
gopubmedrs121913396
geneviewrs121913396
scholarrs121913396
googlers121913396
pharmgkbrs121913396
gwascentralrs121913396
openSNPrs121913396
23andMers121913396
23andMe allrs121913396
SNP Nexus

SNPshotrs121913396
SNPdbers121913396
MSV3drs121913396
GWAS Ctlgrs121913396
Max Magnitude0
OMIM116806
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121913396(C,G,T;C,G,T)
Alt rs121913396(C,G,T;C,G,T)
Reference rs121913396(A;A)
Significance Pathogenic
Disease Pilomatrixoma not provided
Variation info
Gene CTNNB1
CLNDBN Pilomatrixoma not provided
Reversed 0
HGVS NC_000003.11:g.41266098A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000019140.4, RCV000087199.2,