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rs398123948

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123948(C;T)
Make rs398123948(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32411868
GeneDMD
is asnp
is mentioned by
dbSNPrs398123948
ebirs398123948
HLIrs398123948
Exacrs398123948
Varsomers398123948
Maprs398123948
PheGenIrs398123948
hapmaprs398123948
1000 genomesrs398123948
hgdprs398123948
ensemblrs398123948
gopubmedrs398123948
geneviewrs398123948
scholarrs398123948
googlers398123948
pharmgkbrs398123948
gwascentralrs398123948
openSNPrs398123948
23andMers398123948
23andMe allrs398123948
SNP Nexus

SNPshotrs398123948
SNPdbers398123948
MSV3drs398123948
GWAS Ctlgrs398123948
Max Magnitude0
ClinVar
Risk rs398123948(T;T)
Alt rs398123948(T;T)
Reference rs398123948(C;C)
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.32429985G>A
CLNSRC HGMD
CLNACC RCV000080601.4, RCV000177467.1, RCV000177468.1,