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rs863224988

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863224988(C;G)
Make rs863224988(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32485102
GeneDMD
is asnp
is mentioned by
dbSNPrs863224988
ebirs863224988
HLIrs863224988
Exacrs863224988
Varsomers863224988
Maprs863224988
PheGenIrs863224988
hapmaprs863224988
1000 genomesrs863224988
hgdprs863224988
ensemblrs863224988
gopubmedrs863224988
geneviewrs863224988
scholarrs863224988
googlers863224988
pharmgkbrs863224988
gwascentralrs863224988
openSNPrs863224988
23andMers863224988
23andMe allrs863224988
SNP Nexus

SNPshotrs863224988
SNPdbers863224988
MSV3drs863224988
GWAS Ctlgrs863224988
Max Magnitude0
ClinVar
Risk rs863224988(G;G)
Alt rs863224988(G;G)
Reference rs863224988(C;C)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32503219G>C
CLNSRC Quest Diagnostics
CLNACC RCV000201114.1,