RS782289759 SURF1

Health Risk Chr 9:133352707
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What This Variant Does
"CLNSIG=5
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 SURF1
rs1588691694 rs121918657 rs781787822 rs1588689993 rs121918658 rs28933402 rs2119081408 rs782316919 rs398122806 rs72619327
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