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rs863224982

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224982(C;C)
Make rs863224982(C;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32595877
GeneDMD
is asnp
is mentioned by
dbSNPrs863224982
ebirs863224982
HLIrs863224982
Exacrs863224982
Varsomers863224982
Maprs863224982
PheGenIrs863224982
hapmaprs863224982
1000 genomesrs863224982
hgdprs863224982
ensemblrs863224982
gopubmedrs863224982
geneviewrs863224982
scholarrs863224982
googlers863224982
pharmgkbrs863224982
gwascentralrs863224982
openSNPrs863224982
23andMers863224982
23andMe allrs863224982
SNP Nexus

SNPshotrs863224982
SNPdbers863224982
MSV3drs863224982
GWAS Ctlgrs863224982
Max Magnitude0
ClinVar
Risk rs863224982(C;C)
Alt rs863224982(C;C)
Reference rs863224982(G;G)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32613994C>G
CLNSRC Quest Diagnostics
CLNACC RCV000201056.1,