Have questions? Visit https://www.reddit.com/r/SNPedia

rs863224992

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863224992(C;G)
Make rs863224992(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32468669
GeneDMD
is asnp
is mentioned by
dbSNPrs863224992
ebirs863224992
HLIrs863224992
Exacrs863224992
Varsomers863224992
Maprs863224992
PheGenIrs863224992
hapmaprs863224992
1000 genomesrs863224992
hgdprs863224992
ensemblrs863224992
gopubmedrs863224992
geneviewrs863224992
scholarrs863224992
googlers863224992
pharmgkbrs863224992
gwascentralrs863224992
openSNPrs863224992
23andMers863224992
23andMe allrs863224992
SNP Nexus

SNPshotrs863224992
SNPdbers863224992
MSV3drs863224992
GWAS Ctlgrs863224992
Max Magnitude0
ClinVar
Risk rs863224992(G;G)
Alt rs863224992(G;G)
Reference rs863224992(C;C)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32486786G>C
CLNSRC Quest Diagnostics
CLNACC RCV000201111.1,