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rs863224987

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863224987(A;T)
Make rs863224987(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32491288
GeneDMD
is asnp
is mentioned by
dbSNPrs863224987
ebirs863224987
HLIrs863224987
Exacrs863224987
Varsomers863224987
Maprs863224987
PheGenIrs863224987
hapmaprs863224987
1000 genomesrs863224987
hgdprs863224987
ensemblrs863224987
gopubmedrs863224987
geneviewrs863224987
scholarrs863224987
googlers863224987
pharmgkbrs863224987
gwascentralrs863224987
openSNPrs863224987
23andMers863224987
23andMe allrs863224987
SNP Nexus

SNPshotrs863224987
SNPdbers863224987
MSV3drs863224987
GWAS Ctlgrs863224987
Max Magnitude0
ClinVar
Risk rs863224987(T;T)
Alt rs863224987(T;T)
Reference rs863224987(A;A)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32509405T>A
CLNSRC Quest Diagnostics
CLNACC RCV000201029.1,