C0040517[trait identifier] AND "Yale Center for Mendelian Genomics, Ya - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1344624	NM_001407.3(CELSR3):c.8765G>A (p.Arg2922His)	CELSR3 (R2922H)	Single nucleotide variant (missense variant)	Tourette syndrome	GLikely risk allele
Select item 1344622	NM_001407.3(CELSR3):c.7853C>T (p.Ala2618Val)	CELSR3 (A2618V)	Single nucleotide variant (missense variant)	Tourette syndrome	GLikely risk allele
Select item 1225855	NM_001407.3(CELSR3):c.2414G>C (p.Ser805Thr)	CELSR3 (S805T)	Single nucleotide variant (missense variant)	not provided	GBenign

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