RS587777600 FDX2

Health Risk Chr 19:10315996
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Associated Conditions
Inborn mitochondrial myopathy
Mitochondrial myopathy
episodic
without optic atrophy and reversible leukoencephalopathy
with optic atrophy and reversible leukoencephalopathy
Inborn mitochondrial myopathy
Mitochondrial myopathy
episodic
without optic atrophy and reversible leukoencephalopathy
with optic atrophy and reversible leukoencephalopathy
Other Variants in FDX2
rs888630930 rs771690392 rs142729488 rs201352690
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