C5193129[trait identifier] AND "Equipe Genetique des Anomalies du Deve - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2500276	NM_001145678.3(KIAA0825):c.3451_3456+13del	KIAA0825	Deletion (splice donor variant)	Polydactyly, postaxial, type a10	GPathogenic
Select item 2500277	NM_001145678.3(KIAA0825):c.2020T>A (p.Tyr674Asn)	KIAA0825, LOC126807453 (Y674N)	Single nucleotide variant (missense variant +1 more)	Polydactyly, postaxial, type a10	GLikely pathogenic