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rs398123890

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123890(-;-)
Make rs398123890(-;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32491420
GeneDMD
is asnp
is mentioned by
dbSNPrs398123890
ebirs398123890
HLIrs398123890
Exacrs398123890
Varsomers398123890
Maprs398123890
PheGenIrs398123890
hapmaprs398123890
1000 genomesrs398123890
hgdprs398123890
ensemblrs398123890
gopubmedrs398123890
geneviewrs398123890
scholarrs398123890
googlers398123890
pharmgkbrs398123890
gwascentralrs398123890
openSNPrs398123890
23andMers398123890
23andMe allrs398123890
SNP Nexus

SNPshotrs398123890
SNPdbers398123890
MSV3drs398123890
GWAS Ctlgrs398123890
Max Magnitude0
ClinVar
Risk rs398123890(;)
Alt rs398123890(;)
Reference rs398123890(G;G)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32509537delC
CLNSRC ClinVar
CLNACC RCV000080502.3,