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rs398123880

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123880(-;-)
Make rs398123880(-;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32844827
GeneDMD
is asnp
is mentioned by
dbSNPrs398123880
ebirs398123880
HLIrs398123880
Exacrs398123880
Varsomers398123880
Maprs398123880
PheGenIrs398123880
hapmaprs398123880
1000 genomesrs398123880
hgdprs398123880
ensemblrs398123880
gopubmedrs398123880
geneviewrs398123880
scholarrs398123880
googlers398123880
pharmgkbrs398123880
gwascentralrs398123880
openSNPrs398123880
23andMers398123880
23andMe allrs398123880
SNP Nexus

SNPshotrs398123880
SNPdbers398123880
MSV3drs398123880
GWAS Ctlgrs398123880
Max Magnitude0
ClinVar
Risk rs398123880(;)
Alt rs398123880(;)
Reference rs398123880(C;C)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32862944delG
CLNSRC ClinVar
CLNACC RCV000080486.3,