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rs794727832

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794727832(C;G)
Make rs794727832(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position31180478
GeneDMD
is asnp
is mentioned by
dbSNPrs794727832
ebirs794727832
HLIrs794727832
Exacrs794727832
Varsomers794727832
Maprs794727832
PheGenIrs794727832
hapmaprs794727832
1000 genomesrs794727832
hgdprs794727832
ensemblrs794727832
gopubmedrs794727832
geneviewrs794727832
scholarrs794727832
googlers794727832
pharmgkbrs794727832
gwascentralrs794727832
openSNPrs794727832
23andMers794727832
23andMe allrs794727832
SNP Nexus

SNPshotrs794727832
SNPdbers794727832
MSV3drs794727832
GWAS Ctlgrs794727832
Max Magnitude0
ClinVar
Risk rs794727832(G;G)
Alt rs794727832(G;G)
Reference rs794727832(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.31198595G>C
CLNSRC
CLNACC RCV000179684.1, RCV000179685.1,