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rs398124011

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398124011(A;T)
Make rs398124011(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32217014
GeneDMD
is asnp
is mentioned by
dbSNPrs398124011
ebirs398124011
HLIrs398124011
Exacrs398124011
Varsomers398124011
Maprs398124011
PheGenIrs398124011
hapmaprs398124011
1000 genomesrs398124011
hgdprs398124011
ensemblrs398124011
gopubmedrs398124011
geneviewrs398124011
scholarrs398124011
googlers398124011
pharmgkbrs398124011
gwascentralrs398124011
openSNPrs398124011
23andMers398124011
23andMe allrs398124011
SNP Nexus

SNPshotrs398124011
SNPdbers398124011
MSV3drs398124011
GWAS Ctlgrs398124011
Max Magnitude0
ClinVar
Risk rs398124011(T;T)
Alt rs398124011(T;T)
Reference rs398124011(A;A)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32235131T>A
CLNSRC ClinVar Emory University
CLNACC RCV000080696.3,