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rs398123894

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398123894(-;-)
Make rs398123894(-;A)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32491376
GeneDMD
is asnp
is mentioned by
dbSNPrs398123894
ebirs398123894
HLIrs398123894
Exacrs398123894
Varsomers398123894
Maprs398123894
PheGenIrs398123894
hapmaprs398123894
1000 genomesrs398123894
hgdprs398123894
ensemblrs398123894
gopubmedrs398123894
geneviewrs398123894
scholarrs398123894
googlers398123894
pharmgkbrs398123894
gwascentralrs398123894
openSNPrs398123894
23andMers398123894
23andMe allrs398123894
SNP Nexus

SNPshotrs398123894
SNPdbers398123894
MSV3drs398123894
GWAS Ctlgrs398123894
Max Magnitude0
ClinVar
Risk rs398123894(;)
Alt rs398123894(;)
Reference rs398123894(A;A)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32509493delT
CLNSRC ClinVar
CLNACC RCV000080507.3,