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rs398123912

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123912(C;T)
Make rs398123912(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32472247
GeneDMD
is asnp
is mentioned by
dbSNPrs398123912
ebirs398123912
HLIrs398123912
Exacrs398123912
Varsomers398123912
Maprs398123912
PheGenIrs398123912
hapmaprs398123912
1000 genomesrs398123912
hgdprs398123912
ensemblrs398123912
gopubmedrs398123912
geneviewrs398123912
scholarrs398123912
googlers398123912
pharmgkbrs398123912
gwascentralrs398123912
openSNPrs398123912
23andMers398123912
23andMe allrs398123912
SNP Nexus

SNPshotrs398123912
SNPdbers398123912
MSV3drs398123912
GWAS Ctlgrs398123912
Max Magnitude0
ClinVar
Risk rs398123912(T;T)
Alt rs398123912(T;T)
Reference rs398123912(C;C)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32490364G>A
CLNSRC HGMD
CLNACC RCV000080530.3,