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rs398123869

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398123869(-;-)
Make rs398123869(-;AAGT)
Make rs398123869(AAGT;AAGT)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32565790
GeneDMD
is asnp
is mentioned by
dbSNPrs398123869
ebirs398123869
HLIrs398123869
Exacrs398123869
Varsomers398123869
Maprs398123869
PheGenIrs398123869
hapmaprs398123869
1000 genomesrs398123869
hgdprs398123869
ensemblrs398123869
gopubmedrs398123869
geneviewrs398123869
scholarrs398123869
googlers398123869
pharmgkbrs398123869
gwascentralrs398123869
openSNPrs398123869
23andMers398123869
23andMe allrs398123869
SNP Nexus

SNPshotrs398123869
SNPdbers398123869
MSV3drs398123869
GWAS Ctlgrs398123869
Max Magnitude0
ClinVar
Risk rs398123869(AAGT;AAGT)
Alt rs398123869(AAGT;AAGT)
Reference rs398123869(;)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32583908_32583911dupACTT
CLNSRC ClinVar
CLNACC RCV000080471.3,