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rs863225017

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863225017(-;A)
Make rs863225017(A;A)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position31209509
GeneDMD
is asnp
is mentioned by
dbSNPrs863225017
ClinGenrs863225017
ebirs863225017
HLIrs863225017
Exacrs863225017
Varsomers863225017
Maprs863225017
PheGenIrs863225017
hapmaprs863225017
1000 genomesrs863225017
hgdprs863225017
ensemblrs863225017
gopubmedrs863225017
geneviewrs863225017
scholarrs863225017
googlers863225017
pharmgkbrs863225017
gwascentralrs863225017
openSNPrs863225017
23andMers863225017
23andMe allrs863225017
SNP Nexus

SNPshotrs863225017
SNPdbers863225017
MSV3drs863225017
GWAS Ctlgrs863225017
Max Magnitude0
ClinVar
Risk rs863225017(A;A)
Alt rs863225017(A;A)
Reference Rs863225017(-;-)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.31227627dupT
CLNSRC Quest Diagnostics
CLNACC RCV000201051.1,