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rs398123883

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123883(C;T)
Make rs398123883(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32501803
GeneDMD
is asnp
is mentioned by
dbSNPrs398123883
ebirs398123883
HLIrs398123883
Exacrs398123883
Varsomers398123883
Maprs398123883
PheGenIrs398123883
hapmaprs398123883
1000 genomesrs398123883
hgdprs398123883
ensemblrs398123883
gopubmedrs398123883
geneviewrs398123883
scholarrs398123883
googlers398123883
pharmgkbrs398123883
gwascentralrs398123883
openSNPrs398123883
23andMers398123883
23andMe allrs398123883
SNP Nexus

SNPshotrs398123883
SNPdbers398123883
MSV3drs398123883
GWAS Ctlgrs398123883
Max Magnitude0
ClinVar
Risk rs398123883(T;T)
Alt rs398123883(T;T)
Reference rs398123883(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.32519920G>A
CLNSRC HGMD
CLNACC RCV000080492.4, RCV000175440.1, RCV000175441.1,