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rs398123961

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs398123961(-;-)
Make rs398123961(-;CT)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32386449
GeneDMD
is asnp
is mentioned by
dbSNPrs398123961
ebirs398123961
HLIrs398123961
Exacrs398123961
Varsomers398123961
Maprs398123961
PheGenIrs398123961
hapmaprs398123961
1000 genomesrs398123961
hgdprs398123961
ensemblrs398123961
gopubmedrs398123961
geneviewrs398123961
scholarrs398123961
googlers398123961
pharmgkbrs398123961
gwascentralrs398123961
openSNPrs398123961
23andMers398123961
23andMe allrs398123961
SNP Nexus

SNPshotrs398123961
SNPdbers398123961
MSV3drs398123961
GWAS Ctlgrs398123961
Max Magnitude0
ClinVar
Risk rs398123961(;)
Alt rs398123961(;)
Reference rs398123961(CT;CT)
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.32404566_32404567delAG
CLNSRC ClinVar
CLNACC RCV000080623.4, RCV000177741.1, RCV000177742.1,