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rs863225012

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863225012(A;A)
Make rs863225012(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position31507314
GeneDMD
is asnp
is mentioned by
dbSNPrs863225012
ebirs863225012
HLIrs863225012
Exacrs863225012
Varsomers863225012
Maprs863225012
PheGenIrs863225012
hapmaprs863225012
1000 genomesrs863225012
hgdprs863225012
ensemblrs863225012
gopubmedrs863225012
geneviewrs863225012
scholarrs863225012
googlers863225012
pharmgkbrs863225012
gwascentralrs863225012
openSNPrs863225012
23andMers863225012
23andMe allrs863225012
SNP Nexus

SNPshotrs863225012
SNPdbers863225012
MSV3drs863225012
GWAS Ctlgrs863225012
Max Magnitude0
ClinVar
Risk rs863225012(A;A)
Alt rs863225012(A;A)
Reference rs863225012(G;G)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.31525431C>T
CLNSRC Quest Diagnostics
CLNACC RCV000201027.1,