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rs398123853

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123853(A;A)
Make rs398123853(A;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32644177
GeneDMD
is asnp
is mentioned by
dbSNPrs398123853
ebirs398123853
HLIrs398123853
Exacrs398123853
Varsomers398123853
Maprs398123853
PheGenIrs398123853
hapmaprs398123853
1000 genomesrs398123853
hgdprs398123853
ensemblrs398123853
gopubmedrs398123853
geneviewrs398123853
scholarrs398123853
googlers398123853
pharmgkbrs398123853
gwascentralrs398123853
openSNPrs398123853
23andMers398123853
23andMe allrs398123853
SNP Nexus

SNPshotrs398123853
SNPdbers398123853
MSV3drs398123853
GWAS Ctlgrs398123853
Max Magnitude0
ClinVar
Risk rs398123853(A;A)
Alt rs398123853(A;A)
Reference rs398123853(C;C)
Significance Pathogenic
Disease Becker muscular dystrophy Duchenne muscular dystrophy Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Becker muscular dystrophy Duchenne muscular dystrophy Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32662294G>C; NC_000023.10:g.32662294G>T
CLNSRC HGMD
CLNACC RCV000174085.1, RCV000174086.1, RCV000080440.3,