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rs398123889

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123889(A;A)
Make rs398123889(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32491463
GeneDMD
is asnp
is mentioned by
dbSNPrs398123889
ebirs398123889
HLIrs398123889
Exacrs398123889
Varsomers398123889
Maprs398123889
PheGenIrs398123889
hapmaprs398123889
1000 genomesrs398123889
hgdprs398123889
ensemblrs398123889
gopubmedrs398123889
geneviewrs398123889
scholarrs398123889
googlers398123889
pharmgkbrs398123889
gwascentralrs398123889
openSNPrs398123889
23andMers398123889
23andMe allrs398123889
SNP Nexus

SNPshotrs398123889
SNPdbers398123889
MSV3drs398123889
GWAS Ctlgrs398123889
Max Magnitude0
ClinVar
Risk rs398123889(A;A)
Alt rs398123889(A;A)
Reference rs398123889(G;G)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32509580C>T
CLNSRC ClinVar Emory University
CLNACC RCV000080500.3,