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rs794727030

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794727030(A;G)
Make rs794727030(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32644315
GeneDMD
is asnp
is mentioned by
dbSNPrs794727030
ebirs794727030
HLIrs794727030
Exacrs794727030
Varsomers794727030
Maprs794727030
PheGenIrs794727030
hapmaprs794727030
1000 genomesrs794727030
hgdprs794727030
ensemblrs794727030
gopubmedrs794727030
geneviewrs794727030
scholarrs794727030
googlers794727030
pharmgkbrs794727030
gwascentralrs794727030
openSNPrs794727030
23andMers794727030
23andMe allrs794727030
SNP Nexus

SNPshotrs794727030
SNPdbers794727030
MSV3drs794727030
GWAS Ctlgrs794727030
Max Magnitude0
ClinVar
Risk rs794727030(G;G)
Alt rs794727030(G;G)
Reference rs794727030(A;A)
Significance Pathogenic
Disease Duchenne muscular dystrophy Becker muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy Becker muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32662432T>C
CLNSRC
CLNACC RCV000174087.1, RCV000174088.1,