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rs794727890

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794727890(A;G)
Make rs794727890(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position31147520
GeneDMD
is asnp
is mentioned by
dbSNPrs794727890
ebirs794727890
HLIrs794727890
Exacrs794727890
Varsomers794727890
Maprs794727890
PheGenIrs794727890
hapmaprs794727890
1000 genomesrs794727890
hgdprs794727890
ensemblrs794727890
gopubmedrs794727890
geneviewrs794727890
scholarrs794727890
googlers794727890
pharmgkbrs794727890
gwascentralrs794727890
openSNPrs794727890
23andMers794727890
23andMe allrs794727890
SNP Nexus

SNPshotrs794727890
SNPdbers794727890
MSV3drs794727890
GWAS Ctlgrs794727890
Max Magnitude0
ClinVar
Risk rs794727890(G;G)
Alt rs794727890(G;G)
Reference rs794727890(A;A)
Significance Pathogenic
Disease Becker muscular dystrophy Dilated cardiomyopathy 3B Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Becker muscular dystrophy Dilated cardiomyopathy 3B Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.31165637T>C
CLNSRC
CLNACC RCV000180065.1, RCV000180066.1, RCV000180067.1,