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rs398123963

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398123963(-;-)
Make rs398123963(-;T)
Make rs398123963(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32386349
GeneDMD
is asnp
is mentioned by
dbSNPrs398123963
ebirs398123963
HLIrs398123963
Exacrs398123963
Varsomers398123963
Maprs398123963
PheGenIrs398123963
hapmaprs398123963
1000 genomesrs398123963
hgdprs398123963
ensemblrs398123963
gopubmedrs398123963
geneviewrs398123963
scholarrs398123963
googlers398123963
pharmgkbrs398123963
gwascentralrs398123963
openSNPrs398123963
23andMers398123963
23andMe allrs398123963
SNP Nexus

SNPshotrs398123963
SNPdbers398123963
MSV3drs398123963
GWAS Ctlgrs398123963
Max Magnitude0
ClinVar
Risk rs398123963(T;T)
Alt rs398123963(T;T)
Reference rs398123963(;)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32404467dupA
CLNSRC ClinVar
CLNACC RCV000080625.3,