"Institute of Human Genetics, University of Wuerzburg"[submitter] AND - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1301867	NM_013275.6(ANKRD11):c.6349_6362del (p.Pro2117fs)	ANKRD11 (P2117fs)	Deletion (frameshift variant)	Neutropenia +1 more	GLikely pathogenic
Select item 1027656	NM_013275.6(ANKRD11):c.4554del (p.Arg1519fs)	ANKRD11 (R1519fs)	Deletion (frameshift variant)	Intellectual disability	GLikely pathogenic