C0040517[trait identifier] AND "Centogene AG - the Rare Disease Compan - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1334050	NM_001281503.2(SLITRK1):c.341A>G (p.Asn114Ser)	SLITRK1 (N114S)	Single nucleotide variant (missense variant)	Tourette syndrome	GUncertain significance
Select item 1333882	NM_002112.4(HDC):c.1568T>A (p.Ile523Asn)	HDC (I490N +1 more)	Single nucleotide variant (missense variant)	Tourette syndrome	GUncertain significance