"Diagnostic Laboratory, Strasbourg University Hospital"[submitter] AND - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 981378	NM_001127644.2(GABRA1):c.888G>T (p.Leu296Phe)	GABRA1 (L296F)	Single nucleotide variant (missense variant)	Intellectual disability	GLikely pathogenic
Select item 981377	NM_001127644.2(GABRA1):c.922G>A (p.Ala308Thr)	GABRA1 (A308T)	Single nucleotide variant (missense variant)	Intellectual disability	GLikely pathogenic