ClinVar Miner

List of variants in gene FDX2, FDX2-ZGLP1 studied for Inborn mitochondrial myopathy

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.1A>T (p.Met1Leu)	rs587777600
NM_001397406.1(FDX2):c.422C>T (p.Pro141Leu)	rs888630930

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