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rs398123865

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123865(C;T)
Make rs398123865(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32573834
GeneDMD
is asnp
is mentioned by
dbSNPrs398123865
ebirs398123865
HLIrs398123865
Exacrs398123865
Varsomers398123865
Maprs398123865
PheGenIrs398123865
hapmaprs398123865
1000 genomesrs398123865
hgdprs398123865
ensemblrs398123865
gopubmedrs398123865
geneviewrs398123865
scholarrs398123865
googlers398123865
pharmgkbrs398123865
gwascentralrs398123865
openSNPrs398123865
23andMers398123865
23andMe allrs398123865
SNP Nexus

SNPshotrs398123865
SNPdbers398123865
MSV3drs398123865
GWAS Ctlgrs398123865
Max Magnitude0
ClinVar
Risk rs398123865(T;T)
Alt rs398123865(T;T)
Reference rs398123865(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.32591951G>A
CLNSRC HGMD
CLNACC RCV000080461.4, RCV000174744.1, RCV000174745.2,