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rs398123937

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123937(A;A)
Make rs398123937(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32463438
GeneDMD
is asnp
is mentioned by
dbSNPrs398123937
ebirs398123937
HLIrs398123937
Exacrs398123937
Varsomers398123937
Maprs398123937
PheGenIrs398123937
hapmaprs398123937
1000 genomesrs398123937
hgdprs398123937
ensemblrs398123937
gopubmedrs398123937
geneviewrs398123937
scholarrs398123937
googlers398123937
pharmgkbrs398123937
gwascentralrs398123937
openSNPrs398123937
23andMers398123937
23andMe allrs398123937
SNP Nexus

SNPshotrs398123937
SNPdbers398123937
MSV3drs398123937
GWAS Ctlgrs398123937
Max Magnitude0
ClinVar
Risk rs398123937(A;A)
Alt rs398123937(A;A)
Reference rs398123937(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.32481555C>T
CLNSRC HGMD
CLNACC RCV000080578.4, RCV000176554.1, RCV000176555.2,