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rs863224983

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863224983(C;T)
Make rs863224983(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32573786
GeneDMD
is asnp
is mentioned by
dbSNPrs863224983
ebirs863224983
HLIrs863224983
Exacrs863224983
Varsomers863224983
Maprs863224983
PheGenIrs863224983
hapmaprs863224983
1000 genomesrs863224983
hgdprs863224983
ensemblrs863224983
gopubmedrs863224983
geneviewrs863224983
scholarrs863224983
googlers863224983
pharmgkbrs863224983
gwascentralrs863224983
openSNPrs863224983
23andMers863224983
23andMe allrs863224983
SNP Nexus

SNPshotrs863224983
SNPdbers863224983
MSV3drs863224983
GWAS Ctlgrs863224983
Max Magnitude0
ClinVar
Risk rs863224983(T;T)
Alt rs863224983(T;T)
Reference rs863224983(C;C)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32591903G>A
CLNSRC Quest Diagnostics
CLNACC RCV000201018.1,