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rs398123997

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123997(G;T)
Make rs398123997(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32342249
GeneDMD
is asnp
is mentioned by
dbSNPrs398123997
ebirs398123997
HLIrs398123997
Exacrs398123997
Varsomers398123997
Maprs398123997
PheGenIrs398123997
hapmaprs398123997
1000 genomesrs398123997
hgdprs398123997
ensemblrs398123997
gopubmedrs398123997
geneviewrs398123997
scholarrs398123997
googlers398123997
pharmgkbrs398123997
gwascentralrs398123997
openSNPrs398123997
23andMers398123997
23andMe allrs398123997
SNP Nexus

SNPshotrs398123997
SNPdbers398123997
MSV3drs398123997
GWAS Ctlgrs398123997
Max Magnitude0
ClinVar
Risk rs398123997(T;T)
Alt rs398123997(T;T)
Reference rs398123997(G;G)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32360366C>A
CLNSRC HGMD
CLNACC RCV000080671.3, RCV000201201.1,