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rs398123859

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398123859(-;-)
Make rs398123859(-;AT)
Make rs398123859(AT;AT)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32849775
GeneDMD
is asnp
is mentioned by
dbSNPrs398123859
ebirs398123859
HLIrs398123859
Exacrs398123859
Varsomers398123859
Maprs398123859
PheGenIrs398123859
hapmaprs398123859
1000 genomesrs398123859
hgdprs398123859
ensemblrs398123859
gopubmedrs398123859
geneviewrs398123859
scholarrs398123859
googlers398123859
pharmgkbrs398123859
gwascentralrs398123859
openSNPrs398123859
23andMers398123859
23andMe allrs398123859
SNP Nexus

SNPshotrs398123859
SNPdbers398123859
MSV3drs398123859
GWAS Ctlgrs398123859
Max Magnitude0
ClinVar
Risk rs398123859(AT;AT)
Alt rs398123859(AT;AT)
Reference rs398123859(;)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32867893_32867894dupAT
CLNSRC ClinVar
CLNACC RCV000080450.3,