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rs878854619

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878854619(G;T)
Make rs878854619(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32573638
GeneDMD
is asnp
is mentioned by
dbSNPrs878854619
ebirs878854619
HLIrs878854619
Exacrs878854619
Varsomers878854619
Maprs878854619
PheGenIrs878854619
hapmaprs878854619
1000 genomesrs878854619
hgdprs878854619
ensemblrs878854619
gopubmedrs878854619
geneviewrs878854619
scholarrs878854619
googlers878854619
pharmgkbrs878854619
gwascentralrs878854619
openSNPrs878854619
23andMers878854619
23andMe allrs878854619
SNP Nexus

SNPshotrs878854619
SNPdbers878854619
MSV3drs878854619
GWAS Ctlgrs878854619
Max Magnitude0
ClinVar
Risk rs878854619(T;T)
Alt rs878854619(T;T)
Reference rs878854619(G;G)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32591755C>A
CLNSRC
CLNACC RCV000231131.1,