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rs863224979

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863224979(C;T)
Make rs863224979(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32644139
GeneDMD
is asnp
is mentioned by
dbSNPrs863224979
ebirs863224979
HLIrs863224979
Exacrs863224979
Varsomers863224979
Maprs863224979
PheGenIrs863224979
hapmaprs863224979
1000 genomesrs863224979
hgdprs863224979
ensemblrs863224979
gopubmedrs863224979
geneviewrs863224979
scholarrs863224979
googlers863224979
pharmgkbrs863224979
gwascentralrs863224979
openSNPrs863224979
23andMers863224979
23andMe allrs863224979
SNP Nexus

SNPshotrs863224979
SNPdbers863224979
MSV3drs863224979
GWAS Ctlgrs863224979
Max Magnitude0
ClinVar
Risk rs863224979(T;T)
Alt rs863224979(T;T)
Reference rs863224979(C;C)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32662256G>A
CLNSRC Quest Diagnostics
CLNACC RCV000201050.1,