C1856439[trait identifier] AND "DBGen Ocular Genomics"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2628023	NM_012293.3(PXDN):c.1838-2A>G	PXDN	Single nucleotide variant (splice acceptor variant)	Glaucoma 3A	GPathogenic
Select item 2628045	NM_000104.4(CYP1B1):c.1064G>C (p.Arg355Pro)	CYP1B1 (R355P)	Single nucleotide variant (missense variant)	Glaucoma 3A	GLikely pathogenic
Select item 2628067	NM_015692.5(CPAMD8):c.3798_3861+1759del	CPAMD8	Deletion (splice acceptor variant +1 more)	Glaucoma 3A	GPathogenic

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