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rs398123969

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398123969(A;T)
Make rs398123969(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32380512
GeneDMD
is asnp
is mentioned by
dbSNPrs398123969
ebirs398123969
HLIrs398123969
Exacrs398123969
Varsomers398123969
Maprs398123969
PheGenIrs398123969
hapmaprs398123969
1000 genomesrs398123969
hgdprs398123969
ensemblrs398123969
gopubmedrs398123969
geneviewrs398123969
scholarrs398123969
googlers398123969
pharmgkbrs398123969
gwascentralrs398123969
openSNPrs398123969
23andMers398123969
23andMe allrs398123969
SNP Nexus

SNPshotrs398123969
SNPdbers398123969
MSV3drs398123969
GWAS Ctlgrs398123969
Max Magnitude0
ClinVar
Risk rs398123969(T;T)
Alt rs398123969(T;T)
Reference rs398123969(A;A)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32398629T>A
CLNSRC ClinVar Emory University
CLNACC RCV000080631.3,