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

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 978900	NM_001278116.2(L1CAM):c.3458-5T>G	L1CAM	Single nucleotide variant (intron variant)	Intellectual disability	GUncertain significance
Select item 978901	NM_001278116.2(L1CAM):c.3226A>C (p.Thr1076Pro)	L1CAM (T1071P +1 more)	Single nucleotide variant (missense variant)	Intellectual disability	GLikely pathogenic