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rs863224984

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224984(A;A)
Make rs863224984(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32573766
GeneDMD
is asnp
is mentioned by
dbSNPrs863224984
ebirs863224984
HLIrs863224984
Exacrs863224984
Varsomers863224984
Maprs863224984
PheGenIrs863224984
hapmaprs863224984
1000 genomesrs863224984
hgdprs863224984
ensemblrs863224984
gopubmedrs863224984
geneviewrs863224984
scholarrs863224984
googlers863224984
pharmgkbrs863224984
gwascentralrs863224984
openSNPrs863224984
23andMers863224984
23andMe allrs863224984
SNP Nexus

SNPshotrs863224984
SNPdbers863224984
MSV3drs863224984
GWAS Ctlgrs863224984
Max Magnitude0
ClinVar
Risk rs863224984(A;A)
Alt rs863224984(A;A)
Reference rs863224984(G;G)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32591883C>T
CLNSRC Quest Diagnostics
CLNACC RCV000201104.1,