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rs863225004

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863225004(C;T)
Make rs863225004(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32343232
GeneDMD
is asnp
is mentioned by
dbSNPrs863225004
ebirs863225004
HLIrs863225004
Exacrs863225004
Varsomers863225004
Maprs863225004
PheGenIrs863225004
hapmaprs863225004
1000 genomesrs863225004
hgdprs863225004
ensemblrs863225004
gopubmedrs863225004
geneviewrs863225004
scholarrs863225004
googlers863225004
pharmgkbrs863225004
gwascentralrs863225004
openSNPrs863225004
23andMers863225004
23andMe allrs863225004
SNP Nexus

SNPshotrs863225004
SNPdbers863225004
MSV3drs863225004
GWAS Ctlgrs863225004
Max Magnitude0
ClinVar
Risk rs863225004(T;T)
Alt rs863225004(T;T)
Reference rs863225004(C;C)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32361349G>A
CLNSRC Quest Diagnostics
CLNACC RCV000201117.1,