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rs794727863

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794727863(C;G)
Make rs794727863(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32809570
GeneDMD
is asnp
is mentioned by
dbSNPrs794727863
ebirs794727863
HLIrs794727863
Exacrs794727863
Varsomers794727863
Maprs794727863
PheGenIrs794727863
hapmaprs794727863
1000 genomesrs794727863
hgdprs794727863
ensemblrs794727863
gopubmedrs794727863
geneviewrs794727863
scholarrs794727863
googlers794727863
pharmgkbrs794727863
gwascentralrs794727863
openSNPrs794727863
23andMers794727863
23andMe allrs794727863
SNP Nexus

SNPshotrs794727863
SNPdbers794727863
MSV3drs794727863
GWAS Ctlgrs794727863
Max Magnitude0
ClinVar
Risk rs794727863(G;G)
Alt rs794727863(G;G)
Reference rs794727863(C;C)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32827687G>C
CLNSRC
CLNACC RCV000179871.1,