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rs398123875

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123875(-;-)
Make rs398123875(-;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32545202
GeneDMD
is asnp
is mentioned by
dbSNPrs398123875
ebirs398123875
HLIrs398123875
Exacrs398123875
Varsomers398123875
Maprs398123875
PheGenIrs398123875
hapmaprs398123875
1000 genomesrs398123875
hgdprs398123875
ensemblrs398123875
gopubmedrs398123875
geneviewrs398123875
scholarrs398123875
googlers398123875
pharmgkbrs398123875
gwascentralrs398123875
openSNPrs398123875
23andMers398123875
23andMe allrs398123875
SNP Nexus

SNPshotrs398123875
SNPdbers398123875
MSV3drs398123875
GWAS Ctlgrs398123875
Max Magnitude0
ClinVar
Risk rs398123875(;)
Alt rs398123875(;)
Reference rs398123875(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.32563319delG
CLNSRC ClinVar
CLNACC RCV000080479.4, RCV000175179.1, RCV000175180.1,