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rs863225002

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863225002(G;T)
Make rs863225002(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32346068
GeneDMD
is asnp
is mentioned by
dbSNPrs863225002
ebirs863225002
HLIrs863225002
Exacrs863225002
Varsomers863225002
Maprs863225002
PheGenIrs863225002
hapmaprs863225002
1000 genomesrs863225002
hgdprs863225002
ensemblrs863225002
gopubmedrs863225002
geneviewrs863225002
scholarrs863225002
googlers863225002
pharmgkbrs863225002
gwascentralrs863225002
openSNPrs863225002
23andMers863225002
23andMe allrs863225002
SNP Nexus

SNPshotrs863225002
SNPdbers863225002
MSV3drs863225002
GWAS Ctlgrs863225002
Max Magnitude0
ClinVar
Risk rs863225002(T;T)
Alt rs863225002(T;T)
Reference rs863225002(G;G)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32364185C>A
CLNSRC Quest Diagnostics
CLNACC RCV000201122.1,