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rs398123903

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123903(C;T)
Make rs398123903(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32485072
GeneDMD
is asnp
is mentioned by
dbSNPrs398123903
ebirs398123903
HLIrs398123903
Exacrs398123903
Varsomers398123903
Maprs398123903
PheGenIrs398123903
hapmaprs398123903
1000 genomesrs398123903
hgdprs398123903
ensemblrs398123903
gopubmedrs398123903
geneviewrs398123903
scholarrs398123903
googlers398123903
pharmgkbrs398123903
gwascentralrs398123903
openSNPrs398123903
23andMers398123903
23andMe allrs398123903
SNP Nexus

SNPshotrs398123903
SNPdbers398123903
MSV3drs398123903
GWAS Ctlgrs398123903
Max Magnitude0
ClinVar
Risk rs398123903(T;T)
Alt rs398123903(T;T)
Reference rs398123903(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.32503189G>A
CLNSRC HGMD
CLNACC RCV000080518.4, RCV000176202.1, RCV000176203.1,