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rs863224864

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863224864(G;G)
Make rs863224864(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position41233614
GeneCTNNB1
is asnp
is mentioned by
dbSNPrs863224864
ebirs863224864
HLIrs863224864
Exacrs863224864
Varsomers863224864
Maprs863224864
PheGenIrs863224864
hapmaprs863224864
1000 genomesrs863224864
hgdprs863224864
ensemblrs863224864
gopubmedrs863224864
geneviewrs863224864
scholarrs863224864
googlers863224864
pharmgkbrs863224864
gwascentralrs863224864
openSNPrs863224864
23andMers863224864
23andMe allrs863224864
SNP Nexus

SNPshotrs863224864
SNPdbers863224864
MSV3drs863224864
GWAS Ctlgrs863224864
Max Magnitude0
ClinVar
Risk rs863224864(G;G)
Alt rs863224864(G;G)
Reference rs863224864(T;T)
Significance Probable-Pathogenic
Disease Mental retardation
Variation info
Gene CTNNB1
CLNDBN Mental retardation, autosomal dominant 19
Reversed 0
HGVS NC_000003.11:g.41275105T>G
CLNSRC
CLNACC RCV000199502.1,