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rs863224991

From SNPedia

Orientationminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863224991(-;T)
Make rs863224991(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32823369
GeneDMD
is asnp
is mentioned by
dbSNPrs863224991
ClinGenrs863224991
ebirs863224991
HLIrs863224991
Exacrs863224991
Varsomers863224991
Maprs863224991
PheGenIrs863224991
hapmaprs863224991
1000 genomesrs863224991
hgdprs863224991
ensemblrs863224991
gopubmedrs863224991
geneviewrs863224991
scholarrs863224991
googlers863224991
pharmgkbrs863224991
gwascentralrs863224991
openSNPrs863224991
23andMers863224991
23andMe allrs863224991
SNP Nexus

SNPshotrs863224991
SNPdbers863224991
MSV3drs863224991
GWAS Ctlgrs863224991
Max Magnitude0
ClinVar
Risk rs863224991(T;T)
Alt rs863224991(T;T)
Reference Rs863224991(;)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32841487dupA
CLNSRC Quest Diagnostics
CLNACC RCV000201042.1,