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rs398123938

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398123938(A;G)
Make rs398123938(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32463436
GeneDMD
is asnp
is mentioned by
dbSNPrs398123938
ebirs398123938
HLIrs398123938
Exacrs398123938
Varsomers398123938
Maprs398123938
PheGenIrs398123938
hapmaprs398123938
1000 genomesrs398123938
hgdprs398123938
ensemblrs398123938
gopubmedrs398123938
geneviewrs398123938
scholarrs398123938
googlers398123938
pharmgkbrs398123938
gwascentralrs398123938
openSNPrs398123938
23andMers398123938
23andMe allrs398123938
SNP Nexus

SNPshotrs398123938
SNPdbers398123938
MSV3drs398123938
GWAS Ctlgrs398123938
Max Magnitude0
ClinVar
Risk rs398123938(G;G)
Alt rs398123938(G;G)
Reference rs398123938(A;A)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32481553T>C
CLNSRC HGMD
CLNACC RCV000080581.3,