List of variants in gene OTX2 reported as likely benign for perceptual disorders

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_021728.4(OTX2):c.*10G>A	rs171978	0.06420
NM_021728.4(OTX2):c.*340del	rs3215889	0.02501
NM_021728.4(OTX2):c.97+12C>T	rs28757218	0.00889
NM_021728.4(OTX2):c.*779G>A	rs138197536	0.00041
NM_021728.4(OTX2):c.*966A>G	rs57390094	0.00006

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