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rs398123905

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123905(C;T)
Make rs398123905(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32484964
GeneDMD
is asnp
is mentioned by
dbSNPrs398123905
ebirs398123905
HLIrs398123905
Exacrs398123905
Varsomers398123905
Maprs398123905
PheGenIrs398123905
hapmaprs398123905
1000 genomesrs398123905
hgdprs398123905
ensemblrs398123905
gopubmedrs398123905
geneviewrs398123905
scholarrs398123905
googlers398123905
pharmgkbrs398123905
gwascentralrs398123905
openSNPrs398123905
23andMers398123905
23andMe allrs398123905
SNP Nexus

SNPshotrs398123905
SNPdbers398123905
MSV3drs398123905
GWAS Ctlgrs398123905
Max Magnitude0
ClinVar
Risk rs398123905(T;T)
Alt rs398123905(T;T)
Reference rs398123905(C;C)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32503081G>A
CLNSRC HGMD
CLNACC RCV000080520.3,