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rs587776437

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587776437(C;C)
Make rs587776437(C;T)
ReferenceGRCh38 38.1/142
ChromosomeMT
Position9478
GeneMT-CO3
is asnp
is mentioned by
dbSNPrs587776437
ebirs587776437
HLIrs587776437
Exacrs587776437
Varsomers587776437
Maprs587776437
PheGenIrs587776437
hapmaprs587776437
1000 genomesrs587776437
hgdprs587776437
ensemblrs587776437
gopubmedrs587776437
geneviewrs587776437
scholarrs587776437
googlers587776437
pharmgkbrs587776437
gwascentralrs587776437
openSNPrs587776437
23andMers587776437
23andMe allrs587776437
SNP Nexus

SNPshotrs587776437
SNPdbers587776437
MSV3drs587776437
GWAS Ctlgrs587776437
Max Magnitude0
ClinVar
Risk rs587776437(C;C)
Alt rs587776437(C;C)
Reference rs587776437(T;T)
Significance Pathogenic
Disease Leigh syndrome
Variation info
Gene COX3
CLNDBN Leigh syndrome
Reversed 0
HGVS NC_012920.1:m.9478T>C
CLNSRC
CLNACC RCV000144007.2,