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rs398123942

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123942(C;T)
Make rs398123942(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32454685
GeneDMD
is asnp
is mentioned by
dbSNPrs398123942
ebirs398123942
HLIrs398123942
Exacrs398123942
Varsomers398123942
Maprs398123942
PheGenIrs398123942
hapmaprs398123942
1000 genomesrs398123942
hgdprs398123942
ensemblrs398123942
gopubmedrs398123942
geneviewrs398123942
scholarrs398123942
googlers398123942
pharmgkbrs398123942
gwascentralrs398123942
openSNPrs398123942
23andMers398123942
23andMe allrs398123942
SNP Nexus

SNPshotrs398123942
SNPdbers398123942
MSV3drs398123942
GWAS Ctlgrs398123942
Max Magnitude0
ClinVar
Risk rs398123942(T;T)
Alt rs398123942(T;T)
Reference rs398123942(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.32472802G>A
CLNSRC HGMD
CLNACC RCV000080586.4, RCV000176665.1, RCV000176666.1,