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rs398123862

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123862(G;T)
Make rs398123862(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32614302
GeneDMD
is asnp
is mentioned by
dbSNPrs398123862
ebirs398123862
HLIrs398123862
Exacrs398123862
Varsomers398123862
Maprs398123862
PheGenIrs398123862
hapmaprs398123862
1000 genomesrs398123862
hgdprs398123862
ensemblrs398123862
gopubmedrs398123862
geneviewrs398123862
scholarrs398123862
googlers398123862
pharmgkbrs398123862
gwascentralrs398123862
openSNPrs398123862
23andMers398123862
23andMe allrs398123862
SNP Nexus

SNPshotrs398123862
SNPdbers398123862
MSV3drs398123862
GWAS Ctlgrs398123862
Max Magnitude0
ClinVar
Risk rs398123862(T;T)
Alt rs398123862(T;T)
Reference rs398123862(G;G)
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.32632419C>A
CLNSRC ClinVar
CLNACC RCV000080454.4, RCV000174326.1, RCV000174327.1,