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rs398124042

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398124042(C;T)
Make rs398124042(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position31836729
GeneDMD
is asnp
is mentioned by
dbSNPrs398124042
ebirs398124042
HLIrs398124042
Exacrs398124042
Varsomers398124042
Maprs398124042
PheGenIrs398124042
hapmaprs398124042
1000 genomesrs398124042
hgdprs398124042
ensemblrs398124042
gopubmedrs398124042
geneviewrs398124042
scholarrs398124042
googlers398124042
pharmgkbrs398124042
gwascentralrs398124042
openSNPrs398124042
23andMers398124042
23andMe allrs398124042
SNP Nexus

SNPshotrs398124042
SNPdbers398124042
MSV3drs398124042
GWAS Ctlgrs398124042
Max Magnitude0
ClinVar
Risk rs398124042(T;T)
Alt rs398124042(T;T)
Reference rs398124042(C;C)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B Becker muscular dystrophy Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B Becker muscular dystrophy Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.31854846G>A
CLNSRC ClinVar Emory University
CLNACC RCV000080751.4, RCV000178690.1, RCV000178691.1,