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rs794727550

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794727550(A;T)
Make rs794727550(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32390100
GeneDMD
is asnp
is mentioned by
dbSNPrs794727550
ebirs794727550
HLIrs794727550
Exacrs794727550
Varsomers794727550
Maprs794727550
PheGenIrs794727550
hapmaprs794727550
1000 genomesrs794727550
hgdprs794727550
ensemblrs794727550
gopubmedrs794727550
geneviewrs794727550
scholarrs794727550
googlers794727550
pharmgkbrs794727550
gwascentralrs794727550
openSNPrs794727550
23andMers794727550
23andMe allrs794727550
SNP Nexus

SNPshotrs794727550
SNPdbers794727550
MSV3drs794727550
GWAS Ctlgrs794727550
Max Magnitude0
ClinVar
Risk rs794727550(T;T)
Alt rs794727550(T;T)
Reference rs794727550(A;A)
Significance Pathogenic
Disease Becker muscular dystrophy Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Becker muscular dystrophy Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32408217T>A
CLNSRC
CLNACC RCV000177554.1, RCV000177555.1,