List of variants in gene PCYT1A reported as uncertain significance 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_001312673.2(PCYT1A):c.983G>A (p.Arg328His)	rs199831548	0.00027
NM_001312673.2(PCYT1A):c.117+5G>A	rs375529354	0.00011
NM_001312673.2(PCYT1A):c.121T>G (p.Leu41Val)

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