"Baylor Genetics"[submitter] AND "LGI1"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1028856	NM_005097.4(LGI1):c.287+1G>A	LGI1	Single nucleotide variant (splice donor variant)	Epilepsy, familial temporal lobe, 1	GLikely pathogenic
Select item 625558	GRCh37/hg19 10q23.33-24.1(chr10:94393383-97219175)	ACSM6, CEP55 +22 more	Copy number loss	not provided	GLikely pathogenic