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rs794727499

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794727499(C;T)
Make rs794727499(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32849781
GeneDMD
is asnp
is mentioned by
dbSNPrs794727499
ebirs794727499
HLIrs794727499
Exacrs794727499
Varsomers794727499
Maprs794727499
PheGenIrs794727499
hapmaprs794727499
1000 genomesrs794727499
hgdprs794727499
ensemblrs794727499
gopubmedrs794727499
geneviewrs794727499
scholarrs794727499
googlers794727499
pharmgkbrs794727499
gwascentralrs794727499
openSNPrs794727499
23andMers794727499
23andMe allrs794727499
SNP Nexus

SNPshotrs794727499
SNPdbers794727499
MSV3drs794727499
GWAS Ctlgrs794727499
Max Magnitude0
ClinVar
Risk rs794727499(T;T)
Alt rs794727499(T;T)
Reference rs794727499(C;C)
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.32867898G>A
CLNSRC
CLNACC RCV000177187.1, RCV000177188.1,