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rs779739455

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs779739455(C;G)
Make rs779739455(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position31968451
GeneDMD
is asnp
is mentioned by
dbSNPrs779739455
ebirs779739455
HLIrs779739455
Exacrs779739455
Varsomers779739455
Maprs779739455
PheGenIrs779739455
hapmaprs779739455
1000 genomesrs779739455
hgdprs779739455
ensemblrs779739455
gopubmedrs779739455
geneviewrs779739455
scholarrs779739455
googlers779739455
pharmgkbrs779739455
gwascentralrs779739455
openSNPrs779739455
23andMers779739455
23andMe allrs779739455
SNP Nexus

SNPshotrs779739455
SNPdbers779739455
MSV3drs779739455
GWAS Ctlgrs779739455
Max Magnitude0
ClinVar
Risk rs779739455(G;G)
Alt rs779739455(G;G)
Reference rs779739455(C;C)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 0
HGVS NC_000023.10:g.31986568C>A
CLNSRC
CLNACC RCV000210931.1,