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rs398123999

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123999(C;T)
Make rs398123999(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32809559
GeneDMD
is asnp
is mentioned by
dbSNPrs398123999
ebirs398123999
HLIrs398123999
Exacrs398123999
Varsomers398123999
Maprs398123999
PheGenIrs398123999
hapmaprs398123999
1000 genomesrs398123999
hgdprs398123999
ensemblrs398123999
gopubmedrs398123999
geneviewrs398123999
scholarrs398123999
googlers398123999
pharmgkbrs398123999
gwascentralrs398123999
openSNPrs398123999
23andMers398123999
23andMe allrs398123999
SNP Nexus

SNPshotrs398123999
SNPdbers398123999
MSV3drs398123999
GWAS Ctlgrs398123999
Max Magnitude0
ClinVar
Risk rs398123999(T;T)
Alt rs398123999(T;T)
Reference rs398123999(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.32827676G>A
CLNSRC HGMD
CLNACC RCV000080674.4, RCV000179874.1, RCV000179875.2,