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rs398123835

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398123835(-;-)
Make rs398123835(-;T)
Make rs398123835(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position31177935
GeneDMD
is asnp
is mentioned by
dbSNPrs398123835
ebirs398123835
HLIrs398123835
Exacrs398123835
Varsomers398123835
Maprs398123835
PheGenIrs398123835
hapmaprs398123835
1000 genomesrs398123835
hgdprs398123835
ensemblrs398123835
gopubmedrs398123835
geneviewrs398123835
scholarrs398123835
googlers398123835
pharmgkbrs398123835
gwascentralrs398123835
openSNPrs398123835
23andMers398123835
23andMe allrs398123835
SNP Nexus

SNPshotrs398123835
SNPdbers398123835
MSV3drs398123835
GWAS Ctlgrs398123835
Max Magnitude0
ClinVar
Risk rs398123835(T;T)
Alt rs398123835(T;T)
Reference rs398123835(;)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.31196053dupA
CLNSRC ClinVar
CLNACC RCV000080416.3,