List of variants in gene PDE1C reported as likely 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_001191057.4(PDE1C):c.778G>T (p.Ala260Ser)	rs775633137	0.00004
NM_001191057.4(PDE1C):c.1900C>T (p.Gln634Ter)
NM_001191057.4(PDE1C):c.2061C>A (p.Tyr687Ter)

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