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rs794727672

From SNPedia

Orientationminus
Make rs794727672(-;-)
Make rs794727672(-;C)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32287581
GeneDMD
is asnp
is mentioned by
dbSNPrs794727672
ebirs794727672
HLIrs794727672
Exacrs794727672
Varsomers794727672
Maprs794727672
PheGenIrs794727672
hapmaprs794727672
1000 genomesrs794727672
hgdprs794727672
ensemblrs794727672
gopubmedrs794727672
geneviewrs794727672
scholarrs794727672
googlers794727672
pharmgkbrs794727672
gwascentralrs794727672
openSNPrs794727672
23andMers794727672
23andMe allrs794727672
SNP Nexus

SNPshotrs794727672
SNPdbers794727672
MSV3drs794727672
GWAS Ctlgrs794727672
Max Magnitude
ClinVar
Risk rs794727672(;)
Alt rs794727672(;)
Reference rs794727672(C;C)
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.32305698delG
CLNSRC
CLNACC RCV000178528.1, RCV000178529.1, RCV000178530.1,