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rs398123983

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123983(-;-)
Make rs398123983(-;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32816467
GeneDMD
is asnp
is mentioned by
dbSNPrs398123983
ebirs398123983
HLIrs398123983
Exacrs398123983
Varsomers398123983
Maprs398123983
PheGenIrs398123983
hapmaprs398123983
1000 genomesrs398123983
hgdprs398123983
ensemblrs398123983
gopubmedrs398123983
geneviewrs398123983
scholarrs398123983
googlers398123983
pharmgkbrs398123983
gwascentralrs398123983
openSNPrs398123983
23andMers398123983
23andMe allrs398123983
SNP Nexus

SNPshotrs398123983
SNPdbers398123983
MSV3drs398123983
GWAS Ctlgrs398123983
Max Magnitude0
ClinVar
Risk rs398123983(;)
Alt rs398123983(;)
Reference rs398123983(G;G)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32834584delC
CLNSRC HGMD
CLNACC RCV000080650.3,