List of variants in gene OPA3 reported as likely benign for not specified

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_025136.4(OPA3):c.231T>C (p.Ala77=)	rs3826860	0.70508
NM_025136.4(OPA3):c.537A>G (p.Lys179=)	rs140105522	0.00158
NM_025136.4(OPA3):c.336G>A (p.Glu112=)	rs146349367	0.00002
NM_025136.4(OPA3):c.123C>G (p.Ile41Met)	rs763083098	0.00001
NM_025136.4(OPA3):c.508G>A (p.Ala170Thr)	rs374639297	0.00001
NM_001017989.3(OPA3):c.222T>G (p.Gly74=)	rs1057520935
NM_025136.4(OPA3):c.216C>T (p.Asn72=)	rs772750356
NM_025136.4(OPA3):c.273C>T (p.Ile91=)	rs369545089
NM_025136.4(OPA3):c.445C>T (p.Leu149=)	rs1057523113
NM_025136.4(OPA3):c.532A>G (p.Lys178Glu)	rs767372876

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