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

rs863224999

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863224999(C;T)
Make rs863224999(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32380626
GeneDMD
is asnp
is mentioned by
dbSNPrs863224999
ebirs863224999
HLIrs863224999
Exacrs863224999
Varsomers863224999
Maprs863224999
PheGenIrs863224999
hapmaprs863224999
1000 genomesrs863224999
hgdprs863224999
ensemblrs863224999
gopubmedrs863224999
geneviewrs863224999
scholarrs863224999
googlers863224999
pharmgkbrs863224999
gwascentralrs863224999
openSNPrs863224999
23andMers863224999
23andMe allrs863224999
SNP Nexus

SNPshotrs863224999
SNPdbers863224999
MSV3drs863224999
GWAS Ctlgrs863224999
Max Magnitude0
ClinVar
Risk rs863224999(T;T)
Alt rs863224999(T;T)
Reference rs863224999(C;C)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32398743G>A
CLNSRC Quest Diagnostics
CLNACC RCV000201158.1,