"Center for Pediatric Genomic Medicine, Children's Mercy Hospital and - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 41890	NM_006950.3(SYN1):c.1699A>G (p.Thr567Ala)	SYN1 (T567A)	Single nucleotide variant (missense variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 252671	NM_006950.3(SYN1):c.1183A>G (p.Ile395Val)	SYN1 (I395V)	Single nucleotide variant (missense variant)	not specified +2 more	GUncertain significance
Select item 139384	NM_006950.3(SYN1):c.152C>G (p.Ala51Gly)	SYN1 (A51G)	Single nucleotide variant (missense variant)	not provided +3 more	GBenign

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