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rs398124053

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398124053(A;A)
Make rs398124053(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position31679564
GeneDMD
is asnp
is mentioned by
dbSNPrs398124053
ebirs398124053
HLIrs398124053
Exacrs398124053
Varsomers398124053
Maprs398124053
PheGenIrs398124053
hapmaprs398124053
1000 genomesrs398124053
hgdprs398124053
ensemblrs398124053
gopubmedrs398124053
geneviewrs398124053
scholarrs398124053
googlers398124053
pharmgkbrs398124053
gwascentralrs398124053
openSNPrs398124053
23andMers398124053
23andMe allrs398124053
SNP Nexus

SNPshotrs398124053
SNPdbers398124053
MSV3drs398124053
GWAS Ctlgrs398124053
Max Magnitude0
ClinVar
Risk rs398124053(A;A)
Alt rs398124053(A;A)
Reference rs398124053(G;G)
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.31697681C>T
CLNSRC ClinVar Emory University
CLNACC RCV000080768.4, RCV000179123.1, RCV000179124.1,