C4539848[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 1333853	NM_001386298.1(CIC):c.6422C>T (p.Pro2141Leu)	CIC (P1232L +2 more)	Single nucleotide variant (missense variant)	Intellectual disability, autosomal dominant 45	GUncertain significance
Select item 1333854	NM_001386298.1(CIC):c.6992C>T (p.Ser2331Leu)	CIC (S1421L +3 more)	Single nucleotide variant (missense variant)	Intellectual disability, autosomal dominant 45	GUncertain significance