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rs398123852

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123852(C;T)
Make rs398123852(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32644202
GeneDMD
is asnp
is mentioned by
dbSNPrs398123852
ebirs398123852
HLIrs398123852
Exacrs398123852
Varsomers398123852
Maprs398123852
PheGenIrs398123852
hapmaprs398123852
1000 genomesrs398123852
hgdprs398123852
ensemblrs398123852
gopubmedrs398123852
geneviewrs398123852
scholarrs398123852
googlers398123852
pharmgkbrs398123852
gwascentralrs398123852
openSNPrs398123852
23andMers398123852
23andMe allrs398123852
SNP Nexus

SNPshotrs398123852
SNPdbers398123852
MSV3drs398123852
GWAS Ctlgrs398123852
Max Magnitude0
ClinVar
Risk rs398123852(G,T;G,T)
Alt rs398123852(G,T;G,T)
Reference rs398123852(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.32662319G>A
CLNSRC HGMD
CLNACC RCV000080439.4, RCV000174089.1, RCV000174090.1,