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rs794727795

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(ATTCTCCTGAGCTG;ATTCTCCTGAGCTG) 0 common in clinvar
Make rs794727795(-;-)
Make rs794727795(-;ATTCTCCTGAGCTG)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32816570
GeneDMD
is asnp
is mentioned by
dbSNPrs794727795
dbSNP (old)rs794727795
ClinGenrs794727795
ebirs794727795
HLIrs794727795
Exacrs794727795
Gnomadrs794727795
Varsomers794727795
Maprs794727795
PheGenIrs794727795
Biobankrs794727795
1000 genomesrs794727795
hgdprs794727795
ensemblrs794727795
gopubmedrs794727795
geneviewrs794727795
scholarrs794727795
googlers794727795
pharmgkbrs794727795
gwascentralrs794727795
openSNPrs794727795
23andMers794727795
23andMe allrs794727795
SNP Nexus

SNPshotrs794727795
SNPdbers794727795
MSV3drs794727795
GWAS Ctlgrs794727795
Max Magnitude0
ClinVar
Risk rs794727795(-;-)
Alt rs794727795(-;-)
Reference Rs794727795(ATTCTCCTGAGCTG;ATTCTCCTGAGCTG)
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.32834687_32834700delCAGCTCAGGAGAAT
CLNSRC
CLNACC RCV000179426.1, RCV000179427.1,