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rs863225009

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863225009(A;A)
Make rs863225009(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position31679430
GeneDMD
is asnp
is mentioned by
dbSNPrs863225009
ebirs863225009
HLIrs863225009
Exacrs863225009
Varsomers863225009
Maprs863225009
PheGenIrs863225009
hapmaprs863225009
1000 genomesrs863225009
hgdprs863225009
ensemblrs863225009
gopubmedrs863225009
geneviewrs863225009
scholarrs863225009
googlers863225009
pharmgkbrs863225009
gwascentralrs863225009
openSNPrs863225009
23andMers863225009
23andMe allrs863225009
SNP Nexus

SNPshotrs863225009
SNPdbers863225009
MSV3drs863225009
GWAS Ctlgrs863225009
Max Magnitude0
ClinVar
Risk rs863225009(A;A)
Alt rs863225009(A;A)
Reference rs863225009(G;G)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.31697547C>T
CLNSRC Quest Diagnostics
CLNACC RCV000201020.1,