"OMIM"[submitter] AND "FDX2"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 623644	NM_001397406.1(FDX2):c.422C>T (p.Pro141Leu)	FDX2, FDX2-ZGLP1 (P144L +1 more)	Single nucleotide variant (missense variant)	Inborn mitochondrial myopathy	GLikely pathogenic
Select item 143059	NM_001397406.1(FDX2):c.1A>T (p.Met1Leu)	FDX2, FDX2-ZGLP1 (M4L)	Single nucleotide variant (missense variant +1 more)	not provided +2 more	GConflicting classifications of pathogenicity