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rs794727463

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794727463(A;T)
Make rs794727463(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32441263
GeneDMD
is asnp
is mentioned by
dbSNPrs794727463
ebirs794727463
HLIrs794727463
Exacrs794727463
Varsomers794727463
Maprs794727463
PheGenIrs794727463
hapmaprs794727463
1000 genomesrs794727463
hgdprs794727463
ensemblrs794727463
gopubmedrs794727463
geneviewrs794727463
scholarrs794727463
googlers794727463
pharmgkbrs794727463
gwascentralrs794727463
openSNPrs794727463
23andMers794727463
23andMe allrs794727463
SNP Nexus

SNPshotrs794727463
SNPdbers794727463
MSV3drs794727463
GWAS Ctlgrs794727463
Max Magnitude0
ClinVar
Risk rs794727463(T;T)
Alt rs794727463(T;T)
Reference rs794727463(A;A)
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.32459380T>A
CLNSRC
CLNACC RCV000176871.1, RCV000176872.1,