ClinVar for MedGen (Select 870499) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 598968	NM_001379110.1(SLC9A6):c.1662-19_1662-3del	SLC9A6	Deletion (intron variant)	Autism +14 more	GLikely pathogenic
Select item 373996	NC_012920.1:m.8084A>G	MT-CO2	Single nucleotide variant	Leigh syndrome	GLikely benign
Select item 373995	NC_012920.1:m.15446C>T	MT-CYB	Single nucleotide variant	Ischemic stroke +1 more	GUncertain significance

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