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rs398123845

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398123845(-;-)
Make rs398123845(-;A)
ReferenceGRCh38 38.1/141
ChromosomeX
Position31147298
GeneDMD
is asnp
is mentioned by
dbSNPrs398123845
ebirs398123845
HLIrs398123845
Exacrs398123845
Varsomers398123845
Maprs398123845
PheGenIrs398123845
hapmaprs398123845
1000 genomesrs398123845
hgdprs398123845
ensemblrs398123845
gopubmedrs398123845
geneviewrs398123845
scholarrs398123845
googlers398123845
pharmgkbrs398123845
gwascentralrs398123845
openSNPrs398123845
23andMers398123845
23andMe allrs398123845
SNP Nexus

SNPshotrs398123845
SNPdbers398123845
MSV3drs398123845
GWAS Ctlgrs398123845
Max Magnitude0
ClinVar
Risk rs398123845(;)
Alt rs398123845(;)
Reference rs398123845(A;A)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.31165415delT
CLNSRC ClinVar
CLNACC RCV000080430.3,