List of variants in gene OPA3 reported as benign for Optic Atrophy, Dominant

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_025136.4(OPA3):c.*1294dup	rs74313320
NM_025136.4(OPA3):c.*3111AGC[3]	rs542311224
NM_025136.4(OPA3):c.*4132CCCTG[3]	rs68079762
NM_025136.4(OPA3):c.*4696ATAA[8]	rs58537694
NM_025136.4(OPA3):c.4850_4852del	rs144752998
NM_025136.4(OPA3):c.*986del	rs377547137

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