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rs794727763

From SNPedia

Orientationminus
Make rs794727763(-;-)
Make rs794727763(-;C)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position31627706
GeneDMD
is asnp
is mentioned by
dbSNPrs794727763
ebirs794727763
HLIrs794727763
Exacrs794727763
Varsomers794727763
Maprs794727763
PheGenIrs794727763
hapmaprs794727763
1000 genomesrs794727763
hgdprs794727763
ensemblrs794727763
gopubmedrs794727763
geneviewrs794727763
scholarrs794727763
googlers794727763
pharmgkbrs794727763
gwascentralrs794727763
openSNPrs794727763
23andMers794727763
23andMe allrs794727763
SNP Nexus

SNPshotrs794727763
SNPdbers794727763
MSV3drs794727763
GWAS Ctlgrs794727763
Max Magnitude
ClinVar
Risk rs794727763(;)
Alt rs794727763(;)
Reference rs794727763(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.31645823delG
CLNSRC
CLNACC RCV000179163.1, RCV000179164.1,