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rs398123868

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398123868(A;T)
Make rs398123868(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32565794
GeneDMD
is asnp
is mentioned by
dbSNPrs398123868
ebirs398123868
HLIrs398123868
Exacrs398123868
Varsomers398123868
Maprs398123868
PheGenIrs398123868
hapmaprs398123868
1000 genomesrs398123868
hgdprs398123868
ensemblrs398123868
gopubmedrs398123868
geneviewrs398123868
scholarrs398123868
googlers398123868
pharmgkbrs398123868
gwascentralrs398123868
openSNPrs398123868
23andMers398123868
23andMe allrs398123868
SNP Nexus

SNPshotrs398123868
SNPdbers398123868
MSV3drs398123868
GWAS Ctlgrs398123868
Max Magnitude0
ClinVar
Risk rs398123868(T;T)
Alt rs398123868(T;T)
Reference rs398123868(A;A)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32583911T>A
CLNSRC ClinVar Emory University
CLNACC RCV000080470.3,