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rs398123927

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398123927(A;T)
Make rs398123927(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32468536
GeneDMD
is asnp
is mentioned by
dbSNPrs398123927
ebirs398123927
HLIrs398123927
Exacrs398123927
Varsomers398123927
Maprs398123927
PheGenIrs398123927
hapmaprs398123927
1000 genomesrs398123927
hgdprs398123927
ensemblrs398123927
gopubmedrs398123927
geneviewrs398123927
scholarrs398123927
googlers398123927
pharmgkbrs398123927
gwascentralrs398123927
openSNPrs398123927
23andMers398123927
23andMe allrs398123927
SNP Nexus

SNPshotrs398123927
SNPdbers398123927
MSV3drs398123927
GWAS Ctlgrs398123927
Max Magnitude0
ClinVar
Risk rs398123927(T;T)
Alt rs398123927(T;T)
Reference rs398123927(A;A)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32486653T>A
CLNSRC ClinVar Emory University
CLNACC RCV000080563.3,