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rs398123985

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398123985(A;C)
Make rs398123985(C;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32809613
GeneDMD
is asnp
is mentioned by
dbSNPrs398123985
ebirs398123985
HLIrs398123985
Exacrs398123985
Varsomers398123985
Maprs398123985
PheGenIrs398123985
hapmaprs398123985
1000 genomesrs398123985
hgdprs398123985
ensemblrs398123985
gopubmedrs398123985
geneviewrs398123985
scholarrs398123985
googlers398123985
pharmgkbrs398123985
gwascentralrs398123985
openSNPrs398123985
23andMers398123985
23andMe allrs398123985
SNP Nexus

SNPshotrs398123985
SNPdbers398123985
MSV3drs398123985
GWAS Ctlgrs398123985
Max Magnitude0
ClinVar
Risk rs398123985(C;C)
Alt rs398123985(C;C)
Reference rs398123985(A;A)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32827730T>G
CLNSRC ClinVar
CLNACC RCV000080652.3,