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rs863224976

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863224976(G;G)
Make rs863224976(G;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position31169584
GeneDMD
is asnp
is mentioned by
dbSNPrs863224976
ebirs863224976
HLIrs863224976
Exacrs863224976
Varsomers863224976
Maprs863224976
PheGenIrs863224976
hapmaprs863224976
1000 genomesrs863224976
hgdprs863224976
ensemblrs863224976
gopubmedrs863224976
geneviewrs863224976
scholarrs863224976
googlers863224976
pharmgkbrs863224976
gwascentralrs863224976
openSNPrs863224976
23andMers863224976
23andMe allrs863224976
SNP Nexus

SNPshotrs863224976
SNPdbers863224976
MSV3drs863224976
GWAS Ctlgrs863224976
Max Magnitude0
ClinVar
Risk rs863224976(G;G)
Alt rs863224976(G;G)
Reference rs863224976(T;T)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.31187701A>C
CLNSRC Quest Diagnostics
CLNACC RCV000201187.1,