List of variants in gene OPN1SW reported as pathogenic 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: 3

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HGVS	dbSNP	gnomAD frequency
NC_000007.14:g.128775556C>T	rs104894031	0.00017
NC_000007.14:g.128773786G>A	rs104894033	0.00004
NC_000007.14:g.128774545A>G	rs104894032

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