RS139771078 SCO1

Health Risk Chr 17:10681157
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Associated Conditions
Leigh syndrome
Mitochondrial complex IV deficiency
nuclear type 4
Inborn genetic diseases
Leigh syndrome
Mitochondrial complex IV deficiency
nuclear type 4
Inborn genetic diseases
Other Variants in SCO1
rs587776629 rs104894630 rs587777220 rs61753148 rs766825748 rs751482122 rs766454175 rs774730754 rs770131276 rs371690301
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