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rs267606615

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606615(A;A)
Make rs267606615(A;G)
ReferenceGRCh38 38.1/141
ChromosomeMT
Position9379
GeneMT-ATP6
is asnp
is mentioned by
dbSNPrs267606615
ebirs267606615
HLIrs267606615
Exacrs267606615
Varsomers267606615
Maprs267606615
PheGenIrs267606615
hapmaprs267606615
1000 genomesrs267606615
hgdprs267606615
ensemblrs267606615
gopubmedrs267606615
geneviewrs267606615
scholarrs267606615
googlers267606615
pharmgkbrs267606615
gwascentralrs267606615
openSNPrs267606615
23andMers267606615
23andMe allrs267606615
SNP Nexus

SNPshotrs267606615
SNPdbers267606615
MSV3drs267606615
GWAS Ctlgrs267606615
Max Magnitude0
ClinVar
Risk rs267606615(A;A)
Alt rs267606615(A;A)
Reference rs267606615(G;G)
Significance Pathogenic
Disease Cytochrome-c oxidase deficiency
Variation info
Gene COX3
CLNDBN Cytochrome-c oxidase deficiency
Reversed 0
HGVS NC_012920.1:m.9379G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010293.4,