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rs794727323

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794727323(G;T)
Make rs794727323(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32491420
GeneDMD
is asnp
is mentioned by
dbSNPrs794727323
ebirs794727323
HLIrs794727323
Exacrs794727323
Varsomers794727323
Maprs794727323
PheGenIrs794727323
hapmaprs794727323
1000 genomesrs794727323
hgdprs794727323
ensemblrs794727323
gopubmedrs794727323
geneviewrs794727323
scholarrs794727323
googlers794727323
pharmgkbrs794727323
gwascentralrs794727323
openSNPrs794727323
23andMers794727323
23andMe allrs794727323
SNP Nexus

SNPshotrs794727323
SNPdbers794727323
MSV3drs794727323
GWAS Ctlgrs794727323
Max Magnitude0
ClinVar
Risk rs794727323(T;T)
Alt rs794727323(T;T)
Reference rs794727323(G;G)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32509537C>A
CLNSRC
CLNACC RCV000176079.1,