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rs863224986

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863224986(C;T)
Make rs863224986(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32491492
GeneDMD
is asnp
is mentioned by
dbSNPrs863224986
ebirs863224986
HLIrs863224986
Exacrs863224986
Varsomers863224986
Maprs863224986
PheGenIrs863224986
hapmaprs863224986
1000 genomesrs863224986
hgdprs863224986
ensemblrs863224986
gopubmedrs863224986
geneviewrs863224986
scholarrs863224986
googlers863224986
pharmgkbrs863224986
gwascentralrs863224986
openSNPrs863224986
23andMers863224986
23andMe allrs863224986
SNP Nexus

SNPshotrs863224986
SNPdbers863224986
MSV3drs863224986
GWAS Ctlgrs863224986
Max Magnitude0
ClinVar
Risk rs863224986(T;T)
Alt rs863224986(T;T)
Reference rs863224986(C;C)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32509609G>A
CLNSRC Quest Diagnostics
CLNACC RCV000201181.1,