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rs863224998

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224998(G;T)
Make rs863224998(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32386378
GeneDMD
is asnp
is mentioned by
dbSNPrs863224998
ebirs863224998
HLIrs863224998
Exacrs863224998
Varsomers863224998
Maprs863224998
PheGenIrs863224998
hapmaprs863224998
1000 genomesrs863224998
hgdprs863224998
ensemblrs863224998
gopubmedrs863224998
geneviewrs863224998
scholarrs863224998
googlers863224998
pharmgkbrs863224998
gwascentralrs863224998
openSNPrs863224998
23andMers863224998
23andMe allrs863224998
SNP Nexus

SNPshotrs863224998
SNPdbers863224998
MSV3drs863224998
GWAS Ctlgrs863224998
Max Magnitude0
ClinVar
Risk rs863224998(T;T)
Alt rs863224998(T;T)
Reference rs863224998(G;G)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32404495C>A
CLNSRC Quest Diagnostics
CLNACC RCV000201102.1,