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rs398124093

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398124093(C;T)
Make rs398124093(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position31223062
GeneDMD
is asnp
is mentioned by
dbSNPrs398124093
ebirs398124093
HLIrs398124093
Exacrs398124093
Varsomers398124093
Maprs398124093
PheGenIrs398124093
hapmaprs398124093
1000 genomesrs398124093
hgdprs398124093
ensemblrs398124093
gopubmedrs398124093
geneviewrs398124093
scholarrs398124093
googlers398124093
pharmgkbrs398124093
gwascentralrs398124093
openSNPrs398124093
23andMers398124093
23andMe allrs398124093
SNP Nexus

SNPshotrs398124093
SNPdbers398124093
MSV3drs398124093
GWAS Ctlgrs398124093
Max Magnitude0
ClinVar
Risk rs398124093(T;T)
Alt rs398124093(T;T)
Reference rs398124093(C;C)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.31241179G>A
CLNSRC HGMD
CLNACC RCV000080838.3,