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rs398123871

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123871(G;T)
Make rs398123871(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32844848
GeneDMD
is asnp
is mentioned by
dbSNPrs398123871
ebirs398123871
HLIrs398123871
Exacrs398123871
Varsomers398123871
Maprs398123871
PheGenIrs398123871
hapmaprs398123871
1000 genomesrs398123871
hgdprs398123871
ensemblrs398123871
gopubmedrs398123871
geneviewrs398123871
scholarrs398123871
googlers398123871
pharmgkbrs398123871
gwascentralrs398123871
openSNPrs398123871
23andMers398123871
23andMe allrs398123871
SNP Nexus

SNPshotrs398123871
SNPdbers398123871
MSV3drs398123871
GWAS Ctlgrs398123871
Max Magnitude0
ClinVar
Risk rs398123871(T;T)
Alt rs398123871(T;T)
Reference rs398123871(G;G)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32862965C>A
CLNSRC HGMD
CLNACC RCV000080475.3,