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rs398123909

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123909(A;A)
Make rs398123909(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32472310
GeneDMD
is asnp
is mentioned by
dbSNPrs398123909
ebirs398123909
HLIrs398123909
Exacrs398123909
Varsomers398123909
Maprs398123909
PheGenIrs398123909
hapmaprs398123909
1000 genomesrs398123909
hgdprs398123909
ensemblrs398123909
gopubmedrs398123909
geneviewrs398123909
scholarrs398123909
googlers398123909
pharmgkbrs398123909
gwascentralrs398123909
openSNPrs398123909
23andMers398123909
23andMe allrs398123909
SNP Nexus

SNPshotrs398123909
SNPdbers398123909
MSV3drs398123909
GWAS Ctlgrs398123909
Max Magnitude0
ClinVar
Risk rs398123909(A;A)
Alt rs398123909(A;A)
Reference rs398123909(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.32490427C>T
CLNSRC ClinVar
CLNACC RCV000080525.4, RCV000176301.1, RCV000176302.1,