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rs398123929

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123929(C;T)
Make rs398123929(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32468509
GeneDMD
is asnp
is mentioned by
dbSNPrs398123929
ebirs398123929
HLIrs398123929
Exacrs398123929
Varsomers398123929
Maprs398123929
PheGenIrs398123929
hapmaprs398123929
1000 genomesrs398123929
hgdprs398123929
ensemblrs398123929
gopubmedrs398123929
geneviewrs398123929
scholarrs398123929
googlers398123929
pharmgkbrs398123929
gwascentralrs398123929
openSNPrs398123929
23andMers398123929
23andMe allrs398123929
SNP Nexus

SNPshotrs398123929
SNPdbers398123929
MSV3drs398123929
GWAS Ctlgrs398123929
Max Magnitude0
ClinVar
Risk rs398123929(T;T)
Alt rs398123929(T;T)
Reference rs398123929(C;C)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32486626G>A
CLNSRC HGMD
CLNACC RCV000080565.3, RCV000201197.1,