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rs797044764

From SNPedia

Orientationminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797044764(-;T)
Make rs797044764(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position31820036
GeneDMD
is asnp
is mentioned by
dbSNPrs797044764
ClinGenrs797044764
ebirs797044764
HLIrs797044764
Exacrs797044764
Varsomers797044764
Maprs797044764
PheGenIrs797044764
hapmaprs797044764
1000 genomesrs797044764
hgdprs797044764
ensemblrs797044764
gopubmedrs797044764
geneviewrs797044764
scholarrs797044764
googlers797044764
pharmgkbrs797044764
gwascentralrs797044764
openSNPrs797044764
23andMers797044764
23andMe allrs797044764
SNP Nexus

SNPshotrs797044764
SNPdbers797044764
MSV3drs797044764
GWAS Ctlgrs797044764
Max Magnitude0
ClinVar
Risk rs797044764(T;T)
Alt rs797044764(T;T)
Reference Rs797044764(;)
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.31838154dupA
CLNSRC
CLNACC RCV000179072.1, RCV000179073.1,