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rs863224994

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GGAAGGT;GGAAGGT) 0 common in clinvar
Make rs863224994(-;-)
Make rs863224994(-;GGAAGGT)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32454831
GeneDMD
is asnp
is mentioned by
dbSNPrs863224994
ClinGenrs863224994
ebirs863224994
HLIrs863224994
Exacrs863224994
Varsomers863224994
Maprs863224994
PheGenIrs863224994
hapmaprs863224994
1000 genomesrs863224994
hgdprs863224994
ensemblrs863224994
gopubmedrs863224994
geneviewrs863224994
scholarrs863224994
googlers863224994
pharmgkbrs863224994
gwascentralrs863224994
openSNPrs863224994
23andMers863224994
23andMe allrs863224994
SNP Nexus

SNPshotrs863224994
SNPdbers863224994
MSV3drs863224994
GWAS Ctlgrs863224994
Max Magnitude0
ClinVar
Risk rs863224994(-;-)
Alt rs863224994(-;-)
Reference Rs863224994(GGAAGGT;GGAAGGT)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32472948_32472954delACCTTCC
CLNSRC Quest Diagnostics
CLNACC RCV000201188.1,