"Baylor Genetics"[submitter] AND "PARS2"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 632566	NM_152268.4(PARS2):c.1091C>G (p.Pro364Arg)	PARS2 (P364R)	Single nucleotide variant (missense variant)	Developmental and epileptic encephalopathy, 75 +3 more	GConflicting classifications of pathogenicity
Select item 983148	NM_152268.4(PARS2):c.340G>A (p.Gly114Ser)	PARS2 (G114S)	Single nucleotide variant (missense variant)	Developmental and epileptic encephalopathy, 75	GUncertain significance