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rs398123995

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398123995(A;T)
Make rs398123995(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32343202
GeneDMD
is asnp
is mentioned by
dbSNPrs398123995
ebirs398123995
HLIrs398123995
Exacrs398123995
Varsomers398123995
Maprs398123995
PheGenIrs398123995
hapmaprs398123995
1000 genomesrs398123995
hgdprs398123995
ensemblrs398123995
gopubmedrs398123995
geneviewrs398123995
scholarrs398123995
googlers398123995
pharmgkbrs398123995
gwascentralrs398123995
openSNPrs398123995
23andMers398123995
23andMe allrs398123995
SNP Nexus

SNPshotrs398123995
SNPdbers398123995
MSV3drs398123995
GWAS Ctlgrs398123995
Max Magnitude0
ClinVar
Risk rs398123995(T;T)
Alt rs398123995(T;T)
Reference rs398123995(A;A)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32361319T>A
CLNSRC ClinVar Emory University
CLNACC RCV000080668.3,