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rs398124007

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398124007(G;T)
Make rs398124007(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32287593
GeneDMD
is asnp
is mentioned by
dbSNPrs398124007
ebirs398124007
HLIrs398124007
Exacrs398124007
Varsomers398124007
Maprs398124007
PheGenIrs398124007
hapmaprs398124007
1000 genomesrs398124007
hgdprs398124007
ensemblrs398124007
gopubmedrs398124007
geneviewrs398124007
scholarrs398124007
googlers398124007
pharmgkbrs398124007
gwascentralrs398124007
openSNPrs398124007
23andMers398124007
23andMe allrs398124007
SNP Nexus

SNPshotrs398124007
SNPdbers398124007
MSV3drs398124007
GWAS Ctlgrs398124007
Max Magnitude0
ClinVar
Risk rs398124007(T;T)
Alt rs398124007(T;T)
Reference rs398124007(G;G)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32305710C>A
CLNSRC ClinVar Emory University
CLNACC RCV000080687.3,