C0268548[trait identifier] AND "Centogene AG - the Rare Disease Compan - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1333824	NM_000045.4(ARG1):c.314_317delinsATGC (p.Ile105_Gly106delinsAsnAla)	ARG1, MED23	Indel (missense variant +2 more)	Arginase deficiency	GUncertain significance
Select item 419876	NM_000045.4(ARG1):c.466-1G>C	ARG1, MED23	Single nucleotide variant (splice acceptor variant +1 more)	not provided +1 more	GPathogenic