ClinVar Miner

List of variants in gene FDX2, FDX2-ZGLP1, LOC130063486 studied for Mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 2

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

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