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rs863224996

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863224996(A;G)
Make rs863224996(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32816642
GeneDMD
is asnp
is mentioned by
dbSNPrs863224996
ebirs863224996
HLIrs863224996
Exacrs863224996
Varsomers863224996
Maprs863224996
PheGenIrs863224996
hapmaprs863224996
1000 genomesrs863224996
hgdprs863224996
ensemblrs863224996
gopubmedrs863224996
geneviewrs863224996
scholarrs863224996
googlers863224996
pharmgkbrs863224996
gwascentralrs863224996
openSNPrs863224996
23andMers863224996
23andMe allrs863224996
SNP Nexus

SNPshotrs863224996
SNPdbers863224996
MSV3drs863224996
GWAS Ctlgrs863224996
Max Magnitude0
ClinVar
Risk rs863224996(G;G)
Alt rs863224996(G;G)
Reference rs863224996(A;A)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32834759T>C
CLNSRC Quest Diagnostics
CLNACC RCV000201147.1,