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rs398123854

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398123854(-;-)
Make rs398123854(-;G)
Make rs398123854(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32644156
GeneDMD
is asnp
is mentioned by
dbSNPrs398123854
ebirs398123854
HLIrs398123854
Exacrs398123854
Varsomers398123854
Maprs398123854
PheGenIrs398123854
hapmaprs398123854
1000 genomesrs398123854
hgdprs398123854
ensemblrs398123854
gopubmedrs398123854
geneviewrs398123854
scholarrs398123854
googlers398123854
pharmgkbrs398123854
gwascentralrs398123854
openSNPrs398123854
23andMers398123854
23andMe allrs398123854
SNP Nexus

SNPshotrs398123854
SNPdbers398123854
MSV3drs398123854
GWAS Ctlgrs398123854
Max Magnitude0
ClinVar
Risk rs398123854(G;G)
Alt rs398123854(G;G)
Reference rs398123854(;)
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.32662274dupC
CLNSRC ClinVar
CLNACC RCV000080441.3, RCV000174092.1, RCV000174093.1,