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rs863224977

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224977(G;T)
Make rs863224977(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position31169492
GeneDMD
is asnp
is mentioned by
dbSNPrs863224977
ebirs863224977
HLIrs863224977
Exacrs863224977
Varsomers863224977
Maprs863224977
PheGenIrs863224977
hapmaprs863224977
1000 genomesrs863224977
hgdprs863224977
ensemblrs863224977
gopubmedrs863224977
geneviewrs863224977
scholarrs863224977
googlers863224977
pharmgkbrs863224977
gwascentralrs863224977
openSNPrs863224977
23andMers863224977
23andMe allrs863224977
SNP Nexus

SNPshotrs863224977
SNPdbers863224977
MSV3drs863224977
GWAS Ctlgrs863224977
Max Magnitude0
ClinVar
Risk rs863224977(T;T)
Alt rs863224977(T;T)
Reference rs863224977(G;G)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.31187609C>A
CLNSRC Quest Diagnostics
CLNACC RCV000201119.1,