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rs398124003

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CTCA;CTCA) 0 common in clinvar
Make rs398124003(-;-)
Make rs398124003(-;CTCA)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32310182
GeneDMD
is asnp
is mentioned by
dbSNPrs398124003
ebirs398124003
HLIrs398124003
Exacrs398124003
Varsomers398124003
Maprs398124003
PheGenIrs398124003
hapmaprs398124003
1000 genomesrs398124003
hgdprs398124003
ensemblrs398124003
gopubmedrs398124003
geneviewrs398124003
scholarrs398124003
googlers398124003
pharmgkbrs398124003
gwascentralrs398124003
openSNPrs398124003
23andMers398124003
23andMe allrs398124003
SNP Nexus

SNPshotrs398124003
SNPdbers398124003
MSV3drs398124003
GWAS Ctlgrs398124003
Max Magnitude0
ClinVar
Risk rs398124003(;)
Alt rs398124003(;)
Reference rs398124003(CTCA;CTCA)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32328299_32328302delTGAG
CLNSRC ClinVar
CLNACC RCV000080680.3,