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rs863225008

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863225008(G;T)
Make rs863225008(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position31836813
GeneDMD
is asnp
is mentioned by
dbSNPrs863225008
ebirs863225008
HLIrs863225008
Exacrs863225008
Varsomers863225008
Maprs863225008
PheGenIrs863225008
hapmaprs863225008
1000 genomesrs863225008
hgdprs863225008
ensemblrs863225008
gopubmedrs863225008
geneviewrs863225008
scholarrs863225008
googlers863225008
pharmgkbrs863225008
gwascentralrs863225008
openSNPrs863225008
23andMers863225008
23andMe allrs863225008
SNP Nexus

SNPshotrs863225008
SNPdbers863225008
MSV3drs863225008
GWAS Ctlgrs863225008
Max Magnitude0
ClinVar
Risk rs863225008(T;T)
Alt rs863225008(T;T)
Reference rs863225008(G;G)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.31854930C>A
CLNSRC Quest Diagnostics
CLNACC RCV000201085.1,