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rs398123882

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CCAT;CCAT) 0 common in clinvar
Make rs398123882(-;-)
Make rs398123882(-;CCAT)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32501838
GeneDMD
is asnp
is mentioned by
dbSNPrs398123882
ebirs398123882
HLIrs398123882
Exacrs398123882
Varsomers398123882
Maprs398123882
PheGenIrs398123882
hapmaprs398123882
1000 genomesrs398123882
hgdprs398123882
ensemblrs398123882
gopubmedrs398123882
geneviewrs398123882
scholarrs398123882
googlers398123882
pharmgkbrs398123882
gwascentralrs398123882
openSNPrs398123882
23andMers398123882
23andMe allrs398123882
SNP Nexus

SNPshotrs398123882
SNPdbers398123882
MSV3drs398123882
GWAS Ctlgrs398123882
Max Magnitude0
ClinVar
Risk rs398123882(;)
Alt rs398123882(;)
Reference rs398123882(CCAT;CCAT)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B Becker muscular dystrophy Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B Becker muscular dystrophy Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32519955_32519958delATGG
CLNSRC ClinVar
CLNACC RCV000080489.4, RCV000175442.1, RCV000175443.1,