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rs794729005

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794729005(G;T)
Make rs794729005(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32485100
GeneDMD
is asnp
is mentioned by
dbSNPrs794729005
ebirs794729005
HLIrs794729005
Exacrs794729005
Varsomers794729005
Maprs794729005
PheGenIrs794729005
hapmaprs794729005
1000 genomesrs794729005
hgdprs794729005
ensemblrs794729005
gopubmedrs794729005
geneviewrs794729005
scholarrs794729005
googlers794729005
pharmgkbrs794729005
gwascentralrs794729005
openSNPrs794729005
23andMers794729005
23andMe allrs794729005
SNP Nexus

SNPshotrs794729005
SNPdbers794729005
MSV3drs794729005
GWAS Ctlgrs794729005
Max Magnitude0
ClinVar
Risk rs794729005(T;T)
Alt rs794729005(T;T)
Reference rs794729005(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene DMD
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.32503217C>A
CLNSRC
CLNACC RCV000183424.1,