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rs878854366

From SNPedia

Orientationminus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs878854366(-;-)
Make rs878854366(-;AG)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position31169486
GeneDMD
is asnp
is mentioned by
dbSNPrs878854366
ebirs878854366
HLIrs878854366
Exacrs878854366
Varsomers878854366
Maprs878854366
PheGenIrs878854366
hapmaprs878854366
1000 genomesrs878854366
hgdprs878854366
ensemblrs878854366
gopubmedrs878854366
geneviewrs878854366
scholarrs878854366
googlers878854366
pharmgkbrs878854366
gwascentralrs878854366
openSNPrs878854366
23andMers878854366
23andMe allrs878854366
SNP Nexus

SNPshotrs878854366
SNPdbers878854366
MSV3drs878854366
GWAS Ctlgrs878854366
Max Magnitude0
ClinVar
Risk rs878854366(;)
Alt rs878854366(;)
Reference rs878854366(AG;AG)
Significance Probable-Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.31187603_31187604delCT
CLNSRC
CLNACC RCV000226304.1,