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rs878854621

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs878854621(-;-)
Make rs878854621(-;A)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position31679466
GeneDMD
is asnp
is mentioned by
dbSNPrs878854621
ebirs878854621
HLIrs878854621
Exacrs878854621
Varsomers878854621
Maprs878854621
PheGenIrs878854621
hapmaprs878854621
1000 genomesrs878854621
hgdprs878854621
ensemblrs878854621
gopubmedrs878854621
geneviewrs878854621
scholarrs878854621
googlers878854621
pharmgkbrs878854621
gwascentralrs878854621
openSNPrs878854621
23andMers878854621
23andMe allrs878854621
SNP Nexus

SNPshotrs878854621
SNPdbers878854621
MSV3drs878854621
GWAS Ctlgrs878854621
Max Magnitude0
ClinVar
Risk rs878854621(;)
Alt rs878854621(;)
Reference rs878854621(A;A)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.31697583delT
CLNSRC
CLNACC RCV000232091.1,