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rs398123858

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398123858(A;T)
Make rs398123858(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32849777
GeneDMD
is asnp
is mentioned by
dbSNPrs398123858
ebirs398123858
HLIrs398123858
Exacrs398123858
Varsomers398123858
Maprs398123858
PheGenIrs398123858
hapmaprs398123858
1000 genomesrs398123858
hgdprs398123858
ensemblrs398123858
gopubmedrs398123858
geneviewrs398123858
scholarrs398123858
googlers398123858
pharmgkbrs398123858
gwascentralrs398123858
openSNPrs398123858
23andMers398123858
23andMe allrs398123858
SNP Nexus

SNPshotrs398123858
SNPdbers398123858
MSV3drs398123858
GWAS Ctlgrs398123858
Max Magnitude0
ClinVar
Risk rs398123858(T;T)
Alt rs398123858(T;T)
Reference rs398123858(A;A)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32867894T>A
CLNSRC HGMD
CLNACC RCV000080449.3,