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rs398123920

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123920(G;T)
Make rs398123920(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32468584
GeneDMD
is asnp
is mentioned by
dbSNPrs398123920
ebirs398123920
HLIrs398123920
Exacrs398123920
Varsomers398123920
Maprs398123920
PheGenIrs398123920
hapmaprs398123920
1000 genomesrs398123920
hgdprs398123920
ensemblrs398123920
gopubmedrs398123920
geneviewrs398123920
scholarrs398123920
googlers398123920
pharmgkbrs398123920
gwascentralrs398123920
openSNPrs398123920
23andMers398123920
23andMe allrs398123920
SNP Nexus

SNPshotrs398123920
SNPdbers398123920
MSV3drs398123920
GWAS Ctlgrs398123920
Max Magnitude0
ClinVar
Risk rs398123920(T;T)
Alt rs398123920(T;T)
Reference rs398123920(G;G)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32486701C>A
CLNSRC HGMD
CLNACC RCV000080539.3,