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rs398124000

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398124000(C;C)
Make rs398124000(C;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32342097
GeneDMD
is asnp
is mentioned by
dbSNPrs398124000
ebirs398124000
HLIrs398124000
Exacrs398124000
Varsomers398124000
Maprs398124000
PheGenIrs398124000
hapmaprs398124000
1000 genomesrs398124000
hgdprs398124000
ensemblrs398124000
gopubmedrs398124000
geneviewrs398124000
scholarrs398124000
googlers398124000
pharmgkbrs398124000
gwascentralrs398124000
openSNPrs398124000
23andMers398124000
23andMe allrs398124000
SNP Nexus

SNPshotrs398124000
SNPdbers398124000
MSV3drs398124000
GWAS Ctlgrs398124000
Max Magnitude0
ClinVar
Risk rs398124000(C;C)
Alt rs398124000(C;C)
Reference rs398124000(G;G)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32360214C>G
CLNSRC HGMD
CLNACC RCV000080676.3,