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rs398123870

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123870(C;T)
Make rs398123870(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32565704
GeneDMD
is asnp
is mentioned by
dbSNPrs398123870
ebirs398123870
HLIrs398123870
Exacrs398123870
Varsomers398123870
Maprs398123870
PheGenIrs398123870
hapmaprs398123870
1000 genomesrs398123870
hgdprs398123870
ensemblrs398123870
gopubmedrs398123870
geneviewrs398123870
scholarrs398123870
googlers398123870
pharmgkbrs398123870
gwascentralrs398123870
openSNPrs398123870
23andMers398123870
23andMe allrs398123870
SNP Nexus

SNPshotrs398123870
SNPdbers398123870
MSV3drs398123870
GWAS Ctlgrs398123870
Max Magnitude0
ClinVar
Risk rs398123870(T;T)
Alt rs398123870(T;T)
Reference rs398123870(C;C)
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.32583821G>A
CLNSRC HGMD
CLNACC RCV000080473.4, RCV000175054.1, RCV000175055.1,