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

rs863224989

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863224989(A;G)
Make rs863224989(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32823389
GeneDMD
is asnp
is mentioned by
dbSNPrs863224989
ebirs863224989
HLIrs863224989
Exacrs863224989
Varsomers863224989
Maprs863224989
PheGenIrs863224989
hapmaprs863224989
1000 genomesrs863224989
hgdprs863224989
ensemblrs863224989
gopubmedrs863224989
geneviewrs863224989
scholarrs863224989
googlers863224989
pharmgkbrs863224989
gwascentralrs863224989
openSNPrs863224989
23andMers863224989
23andMe allrs863224989
SNP Nexus

SNPshotrs863224989
SNPdbers863224989
MSV3drs863224989
GWAS Ctlgrs863224989
Max Magnitude0
ClinVar
Risk rs863224989(G;G)
Alt rs863224989(G;G)
Reference rs863224989(A;A)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32841506T>C
CLNSRC Quest Diagnostics
CLNACC RCV000201171.1,