RS751459058 FARS2

Health Risk Chr 6:5613185
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What This Variant Does
"CLNSIG=4
Associated Conditions
Combined oxidative phosphorylation defect type 14
Hereditary spastic paraplegia 77
Inborn genetic diseases
See cases
FARS2-related disorder
Combined oxidative phosphorylation defect type 14
Hereditary spastic paraplegia 77
Inborn genetic diseases
See cases
FARS2-related disorder
Other Variants in FARS2
rs397514610 rs397514611 rs397514612 rs148568494 rs1554169353 rs146356199 rs202060864 rs372054960 rs775690041 rs764427452
Ask Dr. Hemsworth about this variant