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rs794727820

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794727820(C;G)
Make rs794727820(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position31323606
GeneDMD
is asnp
is mentioned by
dbSNPrs794727820
ebirs794727820
HLIrs794727820
Exacrs794727820
Varsomers794727820
Maprs794727820
PheGenIrs794727820
hapmaprs794727820
1000 genomesrs794727820
hgdprs794727820
ensemblrs794727820
gopubmedrs794727820
geneviewrs794727820
scholarrs794727820
googlers794727820
pharmgkbrs794727820
gwascentralrs794727820
openSNPrs794727820
23andMers794727820
23andMe allrs794727820
SNP Nexus

SNPshotrs794727820
SNPdbers794727820
MSV3drs794727820
GWAS Ctlgrs794727820
Max Magnitude0
ClinVar
Risk rs794727820(G;G)
Alt rs794727820(G;G)
Reference rs794727820(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.31341723G>C
CLNSRC
CLNACC RCV000179602.1, RCV000179603.1,