List of variants in gene PDE6G 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
NM_002602.4(PDE6G):c.146+1G>T
NM_002602.4(PDE6G):c.187+1G>T	rs1598717056
NM_002602.4(PDE6G):c.206del (p.Pro69fs)	rs1555692916

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