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rs794727359

From SNPedia

Orientationminus
Make rs794727359(-;-)
Make rs794727359(-;GA)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32472179
GeneDMD
is asnp
is mentioned by
dbSNPrs794727359
ebirs794727359
HLIrs794727359
Exacrs794727359
Varsomers794727359
Maprs794727359
PheGenIrs794727359
hapmaprs794727359
1000 genomesrs794727359
hgdprs794727359
ensemblrs794727359
gopubmedrs794727359
geneviewrs794727359
scholarrs794727359
googlers794727359
pharmgkbrs794727359
gwascentralrs794727359
openSNPrs794727359
23andMers794727359
23andMe allrs794727359
SNP Nexus

SNPshotrs794727359
SNPdbers794727359
MSV3drs794727359
GWAS Ctlgrs794727359
Max Magnitude
ClinVar
Risk rs794727359(;)
Alt rs794727359(;)
Reference rs794727359(GA;GA)
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.32490296_32490297delTC
CLNSRC
CLNACC RCV000176305.1, RCV000176306.1,