C0282512[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 1333788	NM_001134407.3(GRIN2A):c.3455A>C (p.Gln1152Pro)	GRIN2A (Q1152P)	Single nucleotide variant (missense variant)	Landau-Kleffner syndrome	GUncertain significance
Select item 1333787	NM_001134407.3(GRIN2A):c.1877C>A (p.Thr626Asn)	GRIN2A (T626N)	Single nucleotide variant (missense variant)	Landau-Kleffner syndrome	GUncertain significance