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rs863224981

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224981(A;A)
Make rs863224981(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32614397
GeneDMD
is asnp
is mentioned by
dbSNPrs863224981
ebirs863224981
HLIrs863224981
Exacrs863224981
Varsomers863224981
Maprs863224981
PheGenIrs863224981
hapmaprs863224981
1000 genomesrs863224981
hgdprs863224981
ensemblrs863224981
gopubmedrs863224981
geneviewrs863224981
scholarrs863224981
googlers863224981
pharmgkbrs863224981
gwascentralrs863224981
openSNPrs863224981
23andMers863224981
23andMe allrs863224981
SNP Nexus

SNPshotrs863224981
SNPdbers863224981
MSV3drs863224981
GWAS Ctlgrs863224981
Max Magnitude0
ClinVar
Risk rs863224981(A;A)
Alt rs863224981(A;A)
Reference rs863224981(G;G)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32632514C>T
CLNSRC Quest Diagnostics
CLNACC RCV000201011.1,