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rs587776435

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587776435(G;G)
Make rs587776435(G;T)
ReferenceGRCh38 38.1/142
ChromosomeMT
Position5523
is asnp
is mentioned by
dbSNPrs587776435
ebirs587776435
HLIrs587776435
Exacrs587776435
Varsomers587776435
Maprs587776435
PheGenIrs587776435
hapmaprs587776435
1000 genomesrs587776435
hgdprs587776435
ensemblrs587776435
gopubmedrs587776435
geneviewrs587776435
scholarrs587776435
googlers587776435
pharmgkbrs587776435
gwascentralrs587776435
openSNPrs587776435
23andMers587776435
23andMe allrs587776435
SNP Nexus

SNPshotrs587776435
SNPdbers587776435
MSV3drs587776435
GWAS Ctlgrs587776435
Max Magnitude0
ClinVar
Risk rs587776435(G;G)
Alt rs587776435(G;G)
Reference rs587776435(T;T)
Significance Pathogenic
Disease Leigh syndrome
Variation info
Gene
CLNDBN Leigh syndrome
Reversed 0
HGVS NC_012920.1:m.5523T>G
CLNSRC
CLNACC RCV000144001.2,