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rs398123888

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123888(C;T)
Make rs398123888(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32491480
GeneDMD
is asnp
is mentioned by
dbSNPrs398123888
ebirs398123888
HLIrs398123888
Exacrs398123888
Varsomers398123888
Maprs398123888
PheGenIrs398123888
hapmaprs398123888
1000 genomesrs398123888
hgdprs398123888
ensemblrs398123888
gopubmedrs398123888
geneviewrs398123888
scholarrs398123888
googlers398123888
pharmgkbrs398123888
gwascentralrs398123888
openSNPrs398123888
23andMers398123888
23andMe allrs398123888
SNP Nexus

SNPshotrs398123888
SNPdbers398123888
MSV3drs398123888
GWAS Ctlgrs398123888
Max Magnitude0
ClinVar
Risk rs398123888(T;T)
Alt rs398123888(T;T)
Reference rs398123888(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.32509597G>A
CLNSRC HGMD
CLNACC RCV000080499.4, RCV000176073.1, RCV000176074.1,