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rs398123895

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs398123895(-;-)
Make rs398123895(-;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32491352
GeneDMD
is asnp
is mentioned by
dbSNPrs398123895
ebirs398123895
HLIrs398123895
Exacrs398123895
Varsomers398123895
Maprs398123895
PheGenIrs398123895
hapmaprs398123895
1000 genomesrs398123895
hgdprs398123895
ensemblrs398123895
gopubmedrs398123895
geneviewrs398123895
scholarrs398123895
googlers398123895
pharmgkbrs398123895
gwascentralrs398123895
openSNPrs398123895
23andMers398123895
23andMe allrs398123895
SNP Nexus

SNPshotrs398123895
SNPdbers398123895
MSV3drs398123895
GWAS Ctlgrs398123895
Max Magnitude0
ClinVar
Risk rs398123895(;)
Alt rs398123895(;)
Reference rs398123895(T;T)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B Becker muscular dystrophy Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B Becker muscular dystrophy Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32509469delA
CLNSRC ClinVar
CLNACC RCV000080508.4, RCV000176075.1, RCV000176076.1,