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rs398124058

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398124058(C;T)
Make rs398124058(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position31658123
GeneDMD
is asnp
is mentioned by
dbSNPrs398124058
ebirs398124058
HLIrs398124058
Exacrs398124058
Varsomers398124058
Maprs398124058
PheGenIrs398124058
hapmaprs398124058
1000 genomesrs398124058
hgdprs398124058
ensemblrs398124058
gopubmedrs398124058
geneviewrs398124058
scholarrs398124058
googlers398124058
pharmgkbrs398124058
gwascentralrs398124058
openSNPrs398124058
23andMers398124058
23andMe allrs398124058
SNP Nexus

SNPshotrs398124058
SNPdbers398124058
MSV3drs398124058
GWAS Ctlgrs398124058
Max Magnitude0
ClinVar
Risk rs398124058(T;T)
Alt rs398124058(T;T)
Reference rs398124058(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.31676240G>A
CLNSRC ClinVar Emory University
CLNACC RCV000080774.4, RCV000179148.1, RCV000179149.1,