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rs398123861

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123861(C;T)
Make rs398123861(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32614320
GeneDMD
is asnp
is mentioned by
dbSNPrs398123861
ebirs398123861
HLIrs398123861
Exacrs398123861
Varsomers398123861
Maprs398123861
PheGenIrs398123861
hapmaprs398123861
1000 genomesrs398123861
hgdprs398123861
ensemblrs398123861
gopubmedrs398123861
geneviewrs398123861
scholarrs398123861
googlers398123861
pharmgkbrs398123861
gwascentralrs398123861
openSNPrs398123861
23andMers398123861
23andMe allrs398123861
SNP Nexus

SNPshotrs398123861
SNPdbers398123861
MSV3drs398123861
GWAS Ctlgrs398123861
Max Magnitude0
ClinVar
Risk rs398123861(T;T)
Alt rs398123861(T;T)
Reference rs398123861(C;C)
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.32632437G>A
CLNSRC HGMD
CLNACC RCV000080453.4, RCV000174318.1, RCV000174319.1,