C0342803[trait identifier] AND "Gemeinschaftspraxis fuer Humangenetik - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2691719	NM_001385.3(DPYS):c.1064G>A (p.Arg355Gln)	DPYS (R355Q)	Single nucleotide variant (missense variant)	Dihydropyrimidinase deficiency	GLikely pathogenic
Select item 2691788	NM_001385.3(DPYS):c.983G>T (p.Cys328Phe)	DPYS (C328F)	Single nucleotide variant (missense variant)	Dihydropyrimidinase deficiency	GLikely pathogenic