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rs797045526

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797045526(G;T)
Make rs797045526(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position31965029
GeneDMD
is asnp
is mentioned by
dbSNPrs797045526
ebirs797045526
HLIrs797045526
Exacrs797045526
Varsomers797045526
Maprs797045526
PheGenIrs797045526
hapmaprs797045526
1000 genomesrs797045526
hgdprs797045526
ensemblrs797045526
gopubmedrs797045526
geneviewrs797045526
scholarrs797045526
googlers797045526
pharmgkbrs797045526
gwascentralrs797045526
openSNPrs797045526
23andMers797045526
23andMe allrs797045526
SNP Nexus

SNPshotrs797045526
SNPdbers797045526
MSV3drs797045526
GWAS Ctlgrs797045526
Max Magnitude0
ClinVar
Risk rs797045526(T;T)
Alt rs797045526(T;T)
Reference rs797045526(G;G)
Significance Probable-Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.31983146C>A
CLNSRC
CLNACC RCV000192688.1,