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rs794727170

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794727170(C;T)
Make rs794727170(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32565782
GeneDMD
is asnp
is mentioned by
dbSNPrs794727170
ebirs794727170
HLIrs794727170
Exacrs794727170
Varsomers794727170
Maprs794727170
PheGenIrs794727170
hapmaprs794727170
1000 genomesrs794727170
hgdprs794727170
ensemblrs794727170
gopubmedrs794727170
geneviewrs794727170
scholarrs794727170
googlers794727170
pharmgkbrs794727170
gwascentralrs794727170
openSNPrs794727170
23andMers794727170
23andMe allrs794727170
SNP Nexus

SNPshotrs794727170
SNPdbers794727170
MSV3drs794727170
GWAS Ctlgrs794727170
Max Magnitude0
ClinVar
Risk rs794727170(T;T)
Alt rs794727170(T;T)
Reference rs794727170(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.32583899G>A
CLNSRC
CLNACC RCV000175050.1, RCV000175051.1,