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rs587777134

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(T;T) 0 common in clinvar
Make rs587777134(A;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position67606868
GeneCTNNA3
is asnp
is mentioned by
dbSNPrs587777134
ebirs587777134
HLIrs587777134
Exacrs587777134
Varsomers587777134
Maprs587777134
PheGenIrs587777134
hapmaprs587777134
1000 genomesrs587777134
hgdprs587777134
ensemblrs587777134
gopubmedrs587777134
geneviewrs587777134
scholarrs587777134
googlers587777134
pharmgkbrs587777134
gwascentralrs587777134
openSNPrs587777134
23andMers587777134
23andMe allrs587777134
SNP Nexus

SNPshotrs587777134
SNPdbers587777134
MSV3drs587777134
GWAS Ctlgrs587777134
Max Magnitude0
ClinVar
Risk rs587777134(A;A)
Alt rs587777134(A;A)
Reference rs587777134(T;T)
Significance Pathogenic
Disease Arrhythmogenic right ventricular dysplasia
Variation info
Gene CTNNA3
CLNDBN Arrhythmogenic right ventricular dysplasia, familial, 13
Reversed 1
HGVS NC_000010.10:g.69366626A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000087056.3,