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rs398124008

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398124008(C;T)
Make rs398124008(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32287536
GeneDMD
is asnp
is mentioned by
dbSNPrs398124008
ebirs398124008
HLIrs398124008
Exacrs398124008
Varsomers398124008
Maprs398124008
PheGenIrs398124008
hapmaprs398124008
1000 genomesrs398124008
hgdprs398124008
ensemblrs398124008
gopubmedrs398124008
geneviewrs398124008
scholarrs398124008
googlers398124008
pharmgkbrs398124008
gwascentralrs398124008
openSNPrs398124008
23andMers398124008
23andMe allrs398124008
SNP Nexus

SNPshotrs398124008
SNPdbers398124008
MSV3drs398124008
GWAS Ctlgrs398124008
Max Magnitude0
ClinVar
Risk rs398124008(A,T;A,T)
Alt rs398124008(A,T;A,T)
Reference rs398124008(C;C)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32305653G>A
CLNSRC HGMD
CLNACC RCV000080688.3,