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rs863224993

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863224993(C;T)
Make rs863224993(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32463444
GeneDMD
is asnp
is mentioned by
dbSNPrs863224993
ebirs863224993
HLIrs863224993
Exacrs863224993
Varsomers863224993
Maprs863224993
PheGenIrs863224993
hapmaprs863224993
1000 genomesrs863224993
hgdprs863224993
ensemblrs863224993
gopubmedrs863224993
geneviewrs863224993
scholarrs863224993
googlers863224993
pharmgkbrs863224993
gwascentralrs863224993
openSNPrs863224993
23andMers863224993
23andMe allrs863224993
SNP Nexus

SNPshotrs863224993
SNPdbers863224993
MSV3drs863224993
GWAS Ctlgrs863224993
Max Magnitude0
ClinVar
Risk rs863224993(T;T)
Alt rs863224993(T;T)
Reference rs863224993(C;C)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32481561G>A
CLNSRC Quest Diagnostics
CLNACC RCV000201074.1,