ClinVar Miner

List of variants in gene combination LOC130064709, OPA3 reported by Counsyl

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_025136.4(OPA3):c.-7C>G	rs199590627	0.00041
NM_025136.3(OPA3):c.-48_-41delCGCCCCGC	rs886054542
NM_025136.4(OPA3):c.2TGG[2] (p.Val3del)	rs1555736840
NM_025136.4(OPA3):c.61A>T (p.Lys21Ter)	rs1555736814

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