"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "LLGL2"[gen - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 769435	NM_001031803.2(LLGL2):c.2230G>A (p.Ala744Thr)	LLGL2 (A744T)	Single nucleotide variant (missense variant)	not provided	GBenign/Likely benign
Select item 1701331	GRCh37/hg19 17q25.1-25.3(chr17:73481509-81043199)x3	AFMID, ALYREF +146 more	Copy number gain	not provided	GPathogenic
Select item 624519	GRCh37/hg19 17q24.1-25.2(chr17:64159738-74891024)x3	LLGL2, MAP2K6 +119 more	Copy number gain	not provided	GLikely pathogenic

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