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rs398124002

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs398124002(A;A)
Make rs398124002(A;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32310199
GeneDMD
is asnp
is mentioned by
dbSNPrs398124002
ebirs398124002
HLIrs398124002
Exacrs398124002
Varsomers398124002
Maprs398124002
PheGenIrs398124002
hapmaprs398124002
1000 genomesrs398124002
hgdprs398124002
ensemblrs398124002
gopubmedrs398124002
geneviewrs398124002
scholarrs398124002
googlers398124002
pharmgkbrs398124002
gwascentralrs398124002
openSNPrs398124002
23andMers398124002
23andMe allrs398124002
SNP Nexus

SNPshotrs398124002
SNPdbers398124002
MSV3drs398124002
GWAS Ctlgrs398124002
Max Magnitude0
ClinVar
Risk rs398124002(A;A)
Alt rs398124002(A;A)
Reference rs398124002(T;T)
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.32328316A>T
CLNSRC ClinVar Emory University
CLNACC RCV000080679.4, RCV000178497.1, RCV000178498.1,