List of variants in gene OPA3 reported as benign by Breakthrough Genomics, Breakthrough Genomics

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: 25

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HGVS	dbSNP	gnomAD frequency
NM_025136.4(OPA3):c.*6790T>C	rs10422253	0.76137
NM_025136.4(OPA3):c.231T>C (p.Ala77=)	rs3826860	0.70508
NM_025136.4(OPA3):c.*1950G>A	rs4404183	0.69999
NM_025136.4(OPA3):c.*3387G>A	rs3760844	0.69742
NM_025136.4(OPA3):c.*4318T>C	rs4802261	0.69665
NM_025136.4(OPA3):c.*152G>A	rs3826861	0.66267
NM_025136.4(OPA3):c.*6012A>G	rs11083772	0.58619
NM_001017989.3(OPA3):c.143-127C>G	rs12971437	0.37215
NM_025136.4(OPA3):c.*3874G>A	rs62109650	0.21272
NM_025136.4(OPA3):c.*5523G>A	rs57585727	0.13908
NM_025136.4(OPA3):c.*638T>A	rs150575877	0.13761
NM_025136.4(OPA3):c.*5525C>T	rs117230006	0.11420
NM_025136.4(OPA3):c.*3212G>A	rs79317386	0.11233
NM_025136.4(OPA3):c.*4672G>A	rs11669246	0.11223
NM_025136.4(OPA3):c.*3722G>A	rs73568973	0.08874
NM_025136.4(OPA3):c.*2485G>A	rs8106584	0.08485
NM_001017989.3(OPA3):c.*190A>G	rs73568948	0.08298
NM_025136.4(OPA3):c.*577T>C	rs112654759	0.06293
NM_025136.4(OPA3):c.*3878A>G	rs79660166	0.06091
NM_025136.4(OPA3):c.*272G>A	rs7246349	0.05540
NM_025136.4(OPA3):c.*3531G>T	rs112899014	0.05413
NM_025136.4(OPA3):c.*3038G>A	rs73568982	0.04790
NM_025136.4(OPA3):c.*1387C>T	rs73568986	0.04457
NM_025136.4(OPA3):c.142+69G>C	rs62111684	0.03152
NM_025136.4(OPA3):c.*4857A>T	rs4803833

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