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rs398123830

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123830(G;T)
Make rs398123830(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32645101
GeneDMD
is asnp
is mentioned by
dbSNPrs398123830
ebirs398123830
HLIrs398123830
Exacrs398123830
Varsomers398123830
Maprs398123830
PheGenIrs398123830
hapmaprs398123830
1000 genomesrs398123830
hgdprs398123830
ensemblrs398123830
gopubmedrs398123830
geneviewrs398123830
scholarrs398123830
googlers398123830
pharmgkbrs398123830
gwascentralrs398123830
openSNPrs398123830
23andMers398123830
23andMe allrs398123830
SNP Nexus

SNPshotrs398123830
SNPdbers398123830
MSV3drs398123830
GWAS Ctlgrs398123830
Max Magnitude0
ClinVar
Risk rs398123830(T;T)
Alt rs398123830(T;T)
Reference rs398123830(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.32663218C>A
CLNSRC HGMD
CLNACC RCV000080410.4, RCV000173789.1, RCV000173790.1,