List of variants in gene OPA3 reported as not provided

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001017989.3(OPA3):c.481G>A (p.Ala161Thr)	rs1445523438	0.00001
NM_025136.4(OPA3):c.143-1G>C	rs80356523
NM_025136.4(OPA3):c.277G>A (p.Gly93Ser)	rs80356524
NM_025136.4(OPA3):c.313C>G (p.Gln105Glu)	rs80356525
NM_025136.4(OPA3):c.322_339del (p.Gln108_Glu113del)	rs80356526
NM_025136.4(OPA3):c.415C>T (p.Gln139Ter)	rs28937899
NM_025136.4(OPA3):c.439_440del (p.Gly147fs)	rs1425399743

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