RS761097220 FARS2
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Associated Conditions
Combined oxidative phosphorylation defect type 14
Inborn genetic diseases
Hereditary spastic paraplegia 77
FARS2-related disorder
Leigh syndrome
Combined oxidative phosphorylation defect type 14
Inborn genetic diseases
Hereditary spastic paraplegia 77
FARS2-related disorder
Leigh syndrome
Other Variants in FARS2