RS199668725 COX10

Health Risk Chr 17:14102246
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Associated Conditions
Leigh syndrome
Mitochondrial complex IV deficiency
nuclear type 1
Inborn genetic diseases
Leigh syndrome
Mitochondrial complex IV deficiency
nuclear type 1
Inborn genetic diseases
Other Variants in COX10
rs104894560 rs104894555 rs104894556 rs104894557 rs387906383 rs587780910 rs587780911 rs62052075 rs146175179 rs111541535
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