C0268416[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 973546	NM_002772.3(TMPRSS15):c.2325del (p.Lys775fs)	TMPRSS15 (K775fs)	Deletion (frameshift variant)	Enterokinase deficiency +1 more	GPathogenic/Likely pathogenic
Select item 973545	NM_002772.3(TMPRSS15):c.2294del (p.Leu765fs)	TMPRSS15 (L765fs)	Deletion (frameshift variant)	Enterokinase deficiency +1 more	GPathogenic/Likely pathogenic