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rs398124073

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398124073(C;T)
Make rs398124073(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position31496871
GeneDMD
is asnp
is mentioned by
dbSNPrs398124073
ebirs398124073
HLIrs398124073
Exacrs398124073
Varsomers398124073
Maprs398124073
PheGenIrs398124073
hapmaprs398124073
1000 genomesrs398124073
hgdprs398124073
ensemblrs398124073
gopubmedrs398124073
geneviewrs398124073
scholarrs398124073
googlers398124073
pharmgkbrs398124073
gwascentralrs398124073
openSNPrs398124073
23andMers398124073
23andMe allrs398124073
SNP Nexus

SNPshotrs398124073
SNPdbers398124073
MSV3drs398124073
GWAS Ctlgrs398124073
Max Magnitude0
ClinVar
Risk rs398124073(A;A)
Alt rs398124073(A;A)
Reference rs398124073(C;C)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.31514988G>A
CLNSRC HGMD
CLNACC RCV000080801.3,