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rs863225013

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863225013(C;C)
Make rs863225013(C;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position31507279
GeneDMD
is asnp
is mentioned by
dbSNPrs863225013
ebirs863225013
HLIrs863225013
Exacrs863225013
Varsomers863225013
Maprs863225013
PheGenIrs863225013
hapmaprs863225013
1000 genomesrs863225013
hgdprs863225013
ensemblrs863225013
gopubmedrs863225013
geneviewrs863225013
scholarrs863225013
googlers863225013
pharmgkbrs863225013
gwascentralrs863225013
openSNPrs863225013
23andMers863225013
23andMe allrs863225013
SNP Nexus

SNPshotrs863225013
SNPdbers863225013
MSV3drs863225013
GWAS Ctlgrs863225013
Max Magnitude0
ClinVar
Risk rs863225013(C;C)
Alt rs863225013(C;C)
Reference rs863225013(T;T)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.31525396A>G
CLNSRC Quest Diagnostics
CLNACC RCV000201084.1,