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rs863225016

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863225016(A;A)
Make rs863225016(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32849821
GeneDMD
is asnp
is mentioned by
dbSNPrs863225016
ebirs863225016
HLIrs863225016
Exacrs863225016
Varsomers863225016
Maprs863225016
PheGenIrs863225016
hapmaprs863225016
1000 genomesrs863225016
hgdprs863225016
ensemblrs863225016
gopubmedrs863225016
geneviewrs863225016
scholarrs863225016
googlers863225016
pharmgkbrs863225016
gwascentralrs863225016
openSNPrs863225016
23andMers863225016
23andMe allrs863225016
SNP Nexus

SNPshotrs863225016
SNPdbers863225016
MSV3drs863225016
GWAS Ctlgrs863225016
Max Magnitude0
ClinVar
Risk rs863225016(A;A)
Alt rs863225016(A;A)
Reference rs863225016(G;G)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32867938C>T
CLNSRC Quest Diagnostics
CLNACC RCV000201209.1,