Have questions? Visit https://www.reddit.com/r/SNPedia

rs794727422

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794727422(G;T)
Make rs794727422(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32454730
GeneDMD
is asnp
is mentioned by
dbSNPrs794727422
ebirs794727422
HLIrs794727422
Exacrs794727422
Varsomers794727422
Maprs794727422
PheGenIrs794727422
hapmaprs794727422
1000 genomesrs794727422
hgdprs794727422
ensemblrs794727422
gopubmedrs794727422
geneviewrs794727422
scholarrs794727422
googlers794727422
pharmgkbrs794727422
gwascentralrs794727422
openSNPrs794727422
23andMers794727422
23andMe allrs794727422
SNP Nexus

SNPshotrs794727422
SNPdbers794727422
MSV3drs794727422
GWAS Ctlgrs794727422
Max Magnitude0
ClinVar
Risk rs794727422(T;T)
Alt rs794727422(T;T)
Reference rs794727422(G;G)
Significance Pathogenic
Disease Duchenne muscular dystrophy Becker muscular dystrophy Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy Becker muscular dystrophy Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32472847C>A
CLNSRC
CLNACC RCV000176662.1, RCV000176663.1, RCV000176664.1,