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rs794727666

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794727666(A;A)
Make rs794727666(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32342154
GeneDMD
is asnp
is mentioned by
dbSNPrs794727666
ebirs794727666
HLIrs794727666
Exacrs794727666
Varsomers794727666
Maprs794727666
PheGenIrs794727666
hapmaprs794727666
1000 genomesrs794727666
hgdprs794727666
ensemblrs794727666
gopubmedrs794727666
geneviewrs794727666
scholarrs794727666
googlers794727666
pharmgkbrs794727666
gwascentralrs794727666
openSNPrs794727666
23andMers794727666
23andMe allrs794727666
SNP Nexus

SNPshotrs794727666
SNPdbers794727666
MSV3drs794727666
GWAS Ctlgrs794727666
Max Magnitude0
ClinVar
Risk rs794727666(A;A)
Alt rs794727666(A;A)
Reference rs794727666(G;G)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32360271C>T
CLNSRC
CLNACC RCV000178462.1,