rs199913055
This variant is located in the C2orf69 gene.
▶ClinVar annotation
Likely Benign★☆☆☆
1 submitterAbout C2orf69
Involved in oxidative phosphorylation. Located in mitochondrion. Implicated in combined oxidative phosphorylation deficiency 53. [provided by Alliance of Genome Resources, Jul 2025]
View all C2orf69 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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