C3280538[trait identifier] AND "Equipe Genetique des Anomalies du Deve - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 982564	NM_001040616.3(LINS1):c.597del (p.Glu200fs)	LINS1 (E185fs +1 more)	Deletion (frameshift variant +2 more)	Intellectual disability, autosomal recessive 27	GLikely pathogenic
Select item 982565	NM_001040616.3(LINS1):c.557_558del (p.Lys186fs)	LINS1 (K171fs +1 more)	Deletion (frameshift variant +2 more)	Intellectual disability, autosomal recessive 27	GLikely pathogenic