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rs398123832

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123832(C;T)
Make rs398123832(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position31178721
GeneDMD
is asnp
is mentioned by
dbSNPrs398123832
ebirs398123832
HLIrs398123832
Exacrs398123832
Varsomers398123832
Maprs398123832
PheGenIrs398123832
hapmaprs398123832
1000 genomesrs398123832
hgdprs398123832
ensemblrs398123832
gopubmedrs398123832
geneviewrs398123832
scholarrs398123832
googlers398123832
pharmgkbrs398123832
gwascentralrs398123832
openSNPrs398123832
23andMers398123832
23andMe allrs398123832
SNP Nexus

SNPshotrs398123832
SNPdbers398123832
MSV3drs398123832
GWAS Ctlgrs398123832
Max Magnitude0
ClinVar
Risk rs398123832(T;T)
Alt rs398123832(T;T)
Reference rs398123832(C;C)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B Becker muscular dystrophy Duchenne muscular dystrophy not provided
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B Becker muscular dystrophy Duchenne muscular dystrophy not provided
Reversed 1
HGVS NC_000023.10:g.31196838G>A
CLNSRC HGMD
CLNACC RCV000080413.4, RCV000180029.1, RCV000180030.2, RCV000183403.1,