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rs878854618

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878854618(C;T)
Make rs878854618(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32595855
GeneDMD
is asnp
is mentioned by
dbSNPrs878854618
ebirs878854618
HLIrs878854618
Exacrs878854618
Varsomers878854618
Maprs878854618
PheGenIrs878854618
hapmaprs878854618
1000 genomesrs878854618
hgdprs878854618
ensemblrs878854618
gopubmedrs878854618
geneviewrs878854618
scholarrs878854618
googlers878854618
pharmgkbrs878854618
gwascentralrs878854618
openSNPrs878854618
23andMers878854618
23andMe allrs878854618
SNP Nexus

SNPshotrs878854618
SNPdbers878854618
MSV3drs878854618
GWAS Ctlgrs878854618
Max Magnitude0
ClinVar
Risk rs878854618(T;T)
Alt rs878854618(T;T)
Reference rs878854618(C;C)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32613972G>A
CLNSRC
CLNACC RCV000230747.1,