C1838180[trait identifier] AND "Equipe Genetique des Anomalies du Deve - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 827778	NM_004793.4(LONP1):c.2815T>C (p.Tyr939His)	LONP1 (Y743H +2 more)	Single nucleotide variant (missense variant +1 more)	CODAS syndrome	GLikely pathogenic
Select item 827779	NM_004793.4(LONP1):c.1321G>A (p.Glu441Lys)	LONP1 (E245K +2 more)	Single nucleotide variant (missense variant +1 more)	CODAS syndrome +1 more	GConflicting classifications of pathogenicity