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rs863225010

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863225010(A;A)
Make rs863225010(A;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position31657988
GeneDMD
is asnp
is mentioned by
dbSNPrs863225010
ebirs863225010
HLIrs863225010
Exacrs863225010
Varsomers863225010
Maprs863225010
PheGenIrs863225010
hapmaprs863225010
1000 genomesrs863225010
hgdprs863225010
ensemblrs863225010
gopubmedrs863225010
geneviewrs863225010
scholarrs863225010
googlers863225010
pharmgkbrs863225010
gwascentralrs863225010
openSNPrs863225010
23andMers863225010
23andMe allrs863225010
SNP Nexus

SNPshotrs863225010
SNPdbers863225010
MSV3drs863225010
GWAS Ctlgrs863225010
Max Magnitude0
ClinVar
Risk rs863225010(A;A)
Alt rs863225010(A;A)
Reference rs863225010(T;T)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.31676105A>T
CLNSRC Quest Diagnostics
CLNACC RCV000201094.1,