C3714756[trait identifier] AND "Pediatric Genomics Discovery Program, - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 813291	NM_001376.5(DYNC1H1):c.4234C>T (p.His1412Tyr)	DYNC1H1 (H1412Y)	Single nucleotide variant (missense variant)	Intellectual disability	GLikely pathogenic
Select item 813289	NM_001376.5(DYNC1H1):c.10973G>A (p.Gly3658Glu)	DYNC1H1 (G3658E)	Single nucleotide variant (missense variant)	Intellectual disability +1 more	GLikely pathogenic