ClinVar Miner

List of variants studied for Mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001397406.1(FDX2):c.45A>G (p.Leu15=)	rs395782	0.52486
NM_001397406.1(FDX2):c.159T>G (p.Ala53=)	rs378395	0.52347
NM_001397406.1(FDX2):c.1A>T (p.Met1Leu)	rs587777600
NM_001397406.1(FDX2):c.200+4A>G

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