List of variants in gene ACO2 reported as benign for hereditary optic atrophy

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_001098.3(ACO2):c.836-54T>C	rs203320	0.39646
NM_001098.3(ACO2):c.836-118C>T	rs9619974	0.36768
NM_001098.3(ACO2):c.670C>T (p.Leu224=)	rs1799932	0.36650
NM_001098.3(ACO2):c.1032+17C>T	rs203319	0.33591
NM_001098.3(ACO2):c.192A>C (p.Thr64=)	rs137831	0.29094
NM_001098.3(ACO2):c.1370+48A>G	rs12484694	0.18929
NM_001098.3(ACO2):c.174-52G>T	rs2076199

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