List of variants in gene OPA3 reported as uncertain significance by Mayo Clinic Laboratories, Mayo Clinic

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_025136.4(OPA3):c.478C>T (p.Arg160Cys)	rs137978109	0.00127
NM_025136.4(OPA3):c.540G>C (p.Ter180Tyr)	rs774281852	0.00001
NM_025136.4(OPA3):c.410A>C (p.Gln137Pro)	rs372161100

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