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rs863224997

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863224997(C;T)
Make rs863224997(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32390175
GeneDMD
is asnp
is mentioned by
dbSNPrs863224997
ebirs863224997
HLIrs863224997
Exacrs863224997
Varsomers863224997
Maprs863224997
PheGenIrs863224997
hapmaprs863224997
1000 genomesrs863224997
hgdprs863224997
ensemblrs863224997
gopubmedrs863224997
geneviewrs863224997
scholarrs863224997
googlers863224997
pharmgkbrs863224997
gwascentralrs863224997
openSNPrs863224997
23andMers863224997
23andMe allrs863224997
SNP Nexus

SNPshotrs863224997
SNPdbers863224997
MSV3drs863224997
GWAS Ctlgrs863224997
Max Magnitude0
ClinVar
Risk rs863224997(T;T)
Alt rs863224997(T;T)
Reference rs863224997(C;C)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32408292G>A
CLNSRC Quest Diagnostics
CLNACC RCV000201081.1,