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rs794727661

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794727661(-;-)
Make rs794727661(-;A)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32343176
GeneDMD
is asnp
is mentioned by
dbSNPrs794727661
dbSNP (old)rs794727661
ClinGenrs794727661
ebirs794727661
HLIrs794727661
Exacrs794727661
Gnomadrs794727661
Varsomers794727661
Maprs794727661
PheGenIrs794727661
Biobankrs794727661
1000 genomesrs794727661
hgdprs794727661
ensemblrs794727661
gopubmedrs794727661
geneviewrs794727661
scholarrs794727661
googlers794727661
pharmgkbrs794727661
gwascentralrs794727661
openSNPrs794727661
23andMers794727661
23andMe allrs794727661
SNP Nexus

SNPshotrs794727661
SNPdbers794727661
MSV3drs794727661
GWAS Ctlgrs794727661
Max Magnitude0
ClinVar
Risk rs794727661(-;-)
Alt rs794727661(-;-)
Reference Rs794727661(A;A)
Significance Pathogenic
Disease Duchenne muscular dystrophy Becker muscular dystrophy Dilated cardiomyopathy 3B not provided
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy Becker muscular dystrophy Dilated cardiomyopathy 3B not provided
Reversed 1
HGVS NC_000023.10:g.32361293delT
CLNSRC
CLNACC RCV000178433.1, RCV000178434.1, RCV000178435.1, RCV000483538.1,