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rs863225011

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863225011(C;T)
Make rs863225011(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position31627852
GeneDMD
is asnp
is mentioned by
dbSNPrs863225011
ebirs863225011
HLIrs863225011
Exacrs863225011
Varsomers863225011
Maprs863225011
PheGenIrs863225011
hapmaprs863225011
1000 genomesrs863225011
hgdprs863225011
ensemblrs863225011
gopubmedrs863225011
geneviewrs863225011
scholarrs863225011
googlers863225011
pharmgkbrs863225011
gwascentralrs863225011
openSNPrs863225011
23andMers863225011
23andMe allrs863225011
SNP Nexus

SNPshotrs863225011
SNPdbers863225011
MSV3drs863225011
GWAS Ctlgrs863225011
Max Magnitude0
ClinVar
Risk rs863225011(T;T)
Alt rs863225011(T;T)
Reference rs863225011(C;C)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.31645969G>A
CLNSRC Quest Diagnostics
CLNACC RCV000201174.1,