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rs398123885

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs398123885(C;C)
Make rs398123885(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32501753
GeneDMD
is asnp
is mentioned by
dbSNPrs398123885
ebirs398123885
HLIrs398123885
Exacrs398123885
Varsomers398123885
Maprs398123885
PheGenIrs398123885
hapmaprs398123885
1000 genomesrs398123885
hgdprs398123885
ensemblrs398123885
gopubmedrs398123885
geneviewrs398123885
scholarrs398123885
googlers398123885
pharmgkbrs398123885
gwascentralrs398123885
openSNPrs398123885
23andMers398123885
23andMe allrs398123885
SNP Nexus

SNPshotrs398123885
SNPdbers398123885
MSV3drs398123885
GWAS Ctlgrs398123885
Max Magnitude0
ClinVar
Risk rs398123885(C;C)
Alt rs398123885(C;C)
Reference rs398123885(T;T)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32519870A>G
CLNSRC ClinVar
CLNACC RCV000080494.3,