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rs398123842

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398123842(-;-)
Make rs398123842(-;A)
Make rs398123842(A;A)
ReferenceGRCh38 38.1/141
ChromosomeX
Position31147469
GeneDMD
is asnp
is mentioned by
dbSNPrs398123842
ebirs398123842
HLIrs398123842
Exacrs398123842
Varsomers398123842
Maprs398123842
PheGenIrs398123842
hapmaprs398123842
1000 genomesrs398123842
hgdprs398123842
ensemblrs398123842
gopubmedrs398123842
geneviewrs398123842
scholarrs398123842
googlers398123842
pharmgkbrs398123842
gwascentralrs398123842
openSNPrs398123842
23andMers398123842
23andMe allrs398123842
SNP Nexus

SNPshotrs398123842
SNPdbers398123842
MSV3drs398123842
GWAS Ctlgrs398123842
Max Magnitude0
ClinVar
Risk rs398123842(A;A)
Alt rs398123842(A;A)
Reference rs398123842(;)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.31165587dupT
CLNSRC ClinVar
CLNACC RCV000080426.3,