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rs863224980

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224980(A;A)
Make rs863224980(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32644131
GeneDMD
is asnp
is mentioned by
dbSNPrs863224980
ebirs863224980
HLIrs863224980
Exacrs863224980
Varsomers863224980
Maprs863224980
PheGenIrs863224980
hapmaprs863224980
1000 genomesrs863224980
hgdprs863224980
ensemblrs863224980
gopubmedrs863224980
geneviewrs863224980
scholarrs863224980
googlers863224980
pharmgkbrs863224980
gwascentralrs863224980
openSNPrs863224980
23andMers863224980
23andMe allrs863224980
SNP Nexus

SNPshotrs863224980
SNPdbers863224980
MSV3drs863224980
GWAS Ctlgrs863224980
Max Magnitude0
ClinVar
Risk rs863224980(A;A)
Alt rs863224980(A;A)
Reference rs863224980(G;G)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32662248C>T
CLNSRC Quest Diagnostics
CLNACC RCV000201140.1,