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rs398123827

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123827(C;T)
Make rs398123827(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position31180423
GeneDMD
is asnp
is mentioned by
dbSNPrs398123827
ebirs398123827
HLIrs398123827
Exacrs398123827
Varsomers398123827
Maprs398123827
PheGenIrs398123827
hapmaprs398123827
1000 genomesrs398123827
hgdprs398123827
ensemblrs398123827
gopubmedrs398123827
geneviewrs398123827
scholarrs398123827
googlers398123827
pharmgkbrs398123827
gwascentralrs398123827
openSNPrs398123827
23andMers398123827
23andMe allrs398123827
SNP Nexus

SNPshotrs398123827
SNPdbers398123827
MSV3drs398123827
GWAS Ctlgrs398123827
Max Magnitude0
ClinVar
Risk rs398123827(T;T)
Alt rs398123827(T;T)
Reference rs398123827(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.31198540G>A
CLNSRC HGMD
CLNACC RCV000080404.4, RCV000179686.1, RCV000179687.1,