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rs863225005

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863225005(C;T)
Make rs863225005(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32342105
GeneDMD
is asnp
is mentioned by
dbSNPrs863225005
ebirs863225005
HLIrs863225005
Exacrs863225005
Varsomers863225005
Maprs863225005
PheGenIrs863225005
hapmaprs863225005
1000 genomesrs863225005
hgdprs863225005
ensemblrs863225005
gopubmedrs863225005
geneviewrs863225005
scholarrs863225005
googlers863225005
pharmgkbrs863225005
gwascentralrs863225005
openSNPrs863225005
23andMers863225005
23andMe allrs863225005
SNP Nexus

SNPshotrs863225005
SNPdbers863225005
MSV3drs863225005
GWAS Ctlgrs863225005
Max Magnitude0
ClinVar
Risk rs863225005(T;T)
Alt rs863225005(T;T)
Reference rs863225005(C;C)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32360222G>A
CLNSRC Quest Diagnostics
CLNACC RCV000201134.1,