List of variants in gene ACO2 reported as likely benign for Infantile cerebellar-retinal degeneration; Optic atrophy 9

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001098.3(ACO2):c.1038G>A (p.Lys346=)	rs144269243	0.00055
NM_001098.3(ACO2):c.941-19C>T	rs375652573	0.00007
NM_001098.3(ACO2):c.1387G>T (p.Gly463Trp)	rs2006715

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