RS761709212 FARS2

Health Risk Chr 6:5431069
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Associated Conditions
Inborn genetic diseases
Combined oxidative phosphorylation defect type 14
Inborn genetic diseases
Combined oxidative phosphorylation defect type 14
Other Variants in FARS2
rs397514610 rs397514611 rs397514612 rs148568494 rs1554169353 rs146356199 rs202060864 rs751459058 rs372054960 rs775690041
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