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rs398123873

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CA;CA) 0 common in clinvar
Make rs398123873(-;-)
Make rs398123873(-;CA)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32545294
GeneDMD
is asnp
is mentioned by
dbSNPrs398123873
ebirs398123873
HLIrs398123873
Exacrs398123873
Varsomers398123873
Maprs398123873
PheGenIrs398123873
hapmaprs398123873
1000 genomesrs398123873
hgdprs398123873
ensemblrs398123873
gopubmedrs398123873
geneviewrs398123873
scholarrs398123873
googlers398123873
pharmgkbrs398123873
gwascentralrs398123873
openSNPrs398123873
23andMers398123873
23andMe allrs398123873
SNP Nexus

SNPshotrs398123873
SNPdbers398123873
MSV3drs398123873
GWAS Ctlgrs398123873
Max Magnitude0
ClinVar
Risk rs398123873(;)
Alt rs398123873(;)
Reference rs398123873(CA;CA)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32563411_32563412delTG
CLNSRC ClinVar
CLNACC RCV000080477.3,