C4282400[trait identifier] AND "HudsonAlpha Institute for Biotechnolog - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 517140	NM_000168.6(GLI3):c.1343C>T (p.Ala448Val)	GLI3 (A448V)	Single nucleotide variant (missense variant)	Polydactyly, postaxial, type A1 +3 more	GUncertain significance
Select item 1172546	NM_000168.6(GLI3):c.758A>G (p.Asp253Gly)	GLI3 (D253G)	Single nucleotide variant (missense variant)	Polydactyly, postaxial, type A1	GUncertain significance