ClinVar for MedGen (Select 815243) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 620038	NM_004170.6(SLC1A1):c.860C>G (p.Ala287Gly)	SLC1A1 (A287G)	Single nucleotide variant (missense variant)	Schizophrenia 18 +1 more	GLikely benign
Select item 50362	nsv1067898	LOC124210610, LOC130001477 +7 more	Deletion	Schizophrenia 18	GPathogenic