List of variants in gene OPA1 reported as likely benign for Autosomal dominant optic atrophy classic form

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

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_130837.3(OPA1):c.2961C>T (p.Arg987=)	rs35540805	0.00758
NM_130837.3(OPA1):c.2049A>G (p.Val683=)	rs73069703	0.00753
NM_130837.3(OPA1):c.1236A>G (p.Ala412=)	rs150807064	0.00179
NM_130837.3(OPA1):c.32+14C>T	rs201927764	0.00054
NM_130837.3(OPA1):c.653C>T (p.Ser218Phe)	rs200243596	0.00022
NM_130837.3(OPA1):c.2506C>T (p.Arg836Trp)	rs190235251	0.00017
NM_130837.3(OPA1):c.70A>G (p.Ile24Val)	rs201520438	0.00017
NM_130837.3(OPA1):c.530G>T (p.Ser177Ile)	rs150279202	0.00016
NM_130837.3(OPA1):c.2331+10T>C	rs371096629	0.00005
NM_130837.3(OPA1):c.339C>T (p.Tyr113=)	rs779836454	0.00004
NM_130837.3(OPA1):c.617C>T (p.Pro206Leu)	rs772090345	0.00004
NM_130837.3(OPA1):c.1286G>A (p.Gly429Asp)	rs146003075	0.00002
NM_130837.3(OPA1):c.1017G>A (p.Thr339=)	rs758922394
NM_130837.3(OPA1):c.1737G>C (p.Gln579His)	rs538099724
NM_130837.3(OPA1):c.544T>C (p.Phe182Leu)	rs769335936

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