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rs794727770

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794727770(A;C)
Make rs794727770(C;C)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position31478376
GeneDMD
is asnp
is mentioned by
dbSNPrs794727770
ebirs794727770
HLIrs794727770
Exacrs794727770
Varsomers794727770
Maprs794727770
PheGenIrs794727770
hapmaprs794727770
1000 genomesrs794727770
hgdprs794727770
ensemblrs794727770
gopubmedrs794727770
geneviewrs794727770
scholarrs794727770
googlers794727770
pharmgkbrs794727770
gwascentralrs794727770
openSNPrs794727770
23andMers794727770
23andMe allrs794727770
SNP Nexus

SNPshotrs794727770
SNPdbers794727770
MSV3drs794727770
GWAS Ctlgrs794727770
Max Magnitude0
ClinVar
Risk rs794727770(C;C)
Alt rs794727770(C;C)
Reference rs794727770(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.31496493T>G
CLNSRC
CLNACC RCV000179224.1, RCV000179225.1,