"ANGPT2-related disorder"[Disease/phenotype] AND "PreventionGenetics, - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3032006	NM_001118887.2(ANGPT2):c.300T>C (p.Tyr100=)	ANGPT2, MCPH1	Single nucleotide variant (synonymous variant +1 more)	ANGPT2-related disorder	GLikely benign
Select item 3046197	NM_001118887.2(ANGPT2):c.139C>T (p.Leu47=)	ANGPT2, MCPH1	Single nucleotide variant (synonymous variant +1 more)	ANGPT2-related disorder	GLikely benign