Have questions? Visit https://www.reddit.com/r/SNPedia

rs398123867

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123867(A;A)
Make rs398123867(A;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32565808
GeneDMD
is asnp
is mentioned by
dbSNPrs398123867
ebirs398123867
HLIrs398123867
Exacrs398123867
Varsomers398123867
Maprs398123867
PheGenIrs398123867
hapmaprs398123867
1000 genomesrs398123867
hgdprs398123867
ensemblrs398123867
gopubmedrs398123867
geneviewrs398123867
scholarrs398123867
googlers398123867
pharmgkbrs398123867
gwascentralrs398123867
openSNPrs398123867
23andMers398123867
23andMe allrs398123867
SNP Nexus

SNPshotrs398123867
SNPdbers398123867
MSV3drs398123867
GWAS Ctlgrs398123867
Max Magnitude0
ClinVar
Risk rs398123867(A;A)
Alt rs398123867(A;A)
Reference rs398123867(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.32583925G>T
CLNSRC ClinVar Emory University
CLNACC RCV000080469.4, RCV000175052.1, RCV000175053.1,