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rs398123990

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123990(C;T)
Make rs398123990(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32348501
GeneDMD
is asnp
is mentioned by
dbSNPrs398123990
ebirs398123990
HLIrs398123990
Exacrs398123990
Varsomers398123990
Maprs398123990
PheGenIrs398123990
hapmaprs398123990
1000 genomesrs398123990
hgdprs398123990
ensemblrs398123990
gopubmedrs398123990
geneviewrs398123990
scholarrs398123990
googlers398123990
pharmgkbrs398123990
gwascentralrs398123990
openSNPrs398123990
23andMers398123990
23andMe allrs398123990
SNP Nexus

SNPshotrs398123990
SNPdbers398123990
MSV3drs398123990
GWAS Ctlgrs398123990
Max Magnitude0
ClinVar
Risk rs398123990(T;T)
Alt rs398123990(T;T)
Reference rs398123990(C;C)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32366618G>A
CLNSRC ClinVar Emory University
CLNACC RCV000080658.3,