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rs794727861

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794727861(C;T)
Make rs794727861(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32809577
GeneDMD
is asnp
is mentioned by
dbSNPrs794727861
ebirs794727861
HLIrs794727861
Exacrs794727861
Varsomers794727861
Maprs794727861
PheGenIrs794727861
hapmaprs794727861
1000 genomesrs794727861
hgdprs794727861
ensemblrs794727861
gopubmedrs794727861
geneviewrs794727861
scholarrs794727861
googlers794727861
pharmgkbrs794727861
gwascentralrs794727861
openSNPrs794727861
23andMers794727861
23andMe allrs794727861
SNP Nexus

SNPshotrs794727861
SNPdbers794727861
MSV3drs794727861
GWAS Ctlgrs794727861
Max Magnitude0
ClinVar
Risk rs794727861(T;T)
Alt rs794727861(T;T)
Reference rs794727861(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.32827694G>A
CLNSRC
CLNACC RCV000179864.1, RCV000179865.1,