"KYNU-related condition"[Disease/phenotype] AND "PreventionGenetics, p - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 799097	NM_003937.3(KYNU):c.60C>T (p.Leu20=)	KYNU	Single nucleotide variant (synonymous variant)	KYNU-related condition +1 more	GLikely benign
Select item 2632261	NM_003937.3(KYNU):c.373_373+3del	KYNU	Deletion (splice donor variant)	KYNU-related condition	GLikely pathogenic