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

rs863224995

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863224995(C;T)
Make rs863224995(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32823297
GeneDMD
is asnp
is mentioned by
dbSNPrs863224995
ebirs863224995
HLIrs863224995
Exacrs863224995
Varsomers863224995
Maprs863224995
PheGenIrs863224995
hapmaprs863224995
1000 genomesrs863224995
hgdprs863224995
ensemblrs863224995
gopubmedrs863224995
geneviewrs863224995
scholarrs863224995
googlers863224995
pharmgkbrs863224995
gwascentralrs863224995
openSNPrs863224995
23andMers863224995
23andMe allrs863224995
SNP Nexus

SNPshotrs863224995
SNPdbers863224995
MSV3drs863224995
GWAS Ctlgrs863224995
Max Magnitude0
ClinVar
Risk rs863224995(T;T)
Alt rs863224995(T;T)
Reference rs863224995(C;C)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32841414G>A
CLNSRC Quest Diagnostics
CLNACC RCV000201060.1,