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rs398123857

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123857(-;-)
Make rs398123857(-;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32614414
GeneDMD
is asnp
is mentioned by
dbSNPrs398123857
ebirs398123857
HLIrs398123857
Exacrs398123857
Varsomers398123857
Maprs398123857
PheGenIrs398123857
hapmaprs398123857
1000 genomesrs398123857
hgdprs398123857
ensemblrs398123857
gopubmedrs398123857
geneviewrs398123857
scholarrs398123857
googlers398123857
pharmgkbrs398123857
gwascentralrs398123857
openSNPrs398123857
23andMers398123857
23andMe allrs398123857
SNP Nexus

SNPshotrs398123857
SNPdbers398123857
MSV3drs398123857
GWAS Ctlgrs398123857
Max Magnitude0
ClinVar
Risk rs398123857(;)
Alt rs398123857(;)
Reference rs398123857(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.32632531delC
CLNSRC ClinVar
CLNACC RCV000080448.4, RCV000174320.1, RCV000174321.1,