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rs398123958

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123958(-;-)
Make rs398123958(-;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32389533
GeneDMD
is asnp
is mentioned by
dbSNPrs398123958
ebirs398123958
HLIrs398123958
Exacrs398123958
Varsomers398123958
Maprs398123958
PheGenIrs398123958
hapmaprs398123958
1000 genomesrs398123958
hgdprs398123958
ensemblrs398123958
gopubmedrs398123958
geneviewrs398123958
scholarrs398123958
googlers398123958
pharmgkbrs398123958
gwascentralrs398123958
openSNPrs398123958
23andMers398123958
23andMe allrs398123958
SNP Nexus

SNPshotrs398123958
SNPdbers398123958
MSV3drs398123958
GWAS Ctlgrs398123958
Max Magnitude0
ClinVar
Risk rs398123958(;)
Alt rs398123958(;)
Reference rs398123958(G;G)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32407650delC
CLNSRC ClinVar
CLNACC RCV000080618.3,