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rs398123840

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123840(G;T)
Make rs398123840(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32645065
GeneDMD
is asnp
is mentioned by
dbSNPrs398123840
ebirs398123840
HLIrs398123840
Exacrs398123840
Varsomers398123840
Maprs398123840
PheGenIrs398123840
hapmaprs398123840
1000 genomesrs398123840
hgdprs398123840
ensemblrs398123840
gopubmedrs398123840
geneviewrs398123840
scholarrs398123840
googlers398123840
pharmgkbrs398123840
gwascentralrs398123840
openSNPrs398123840
23andMers398123840
23andMe allrs398123840
SNP Nexus

SNPshotrs398123840
SNPdbers398123840
MSV3drs398123840
GWAS Ctlgrs398123840
Max Magnitude0
ClinVar
Risk rs398123840(T;T)
Alt rs398123840(T;T)
Reference rs398123840(G;G)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B Becker muscular dystrophy Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B Becker muscular dystrophy Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32663182C>A
CLNSRC ClinVar Emory University
CLNACC RCV000080422.4, RCV000173787.1, RCV000173788.1,