"PreventionGenetics, part of Exact Sciences"[submitter] AND "SYN2"[gen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3038848	NM_133625.6(SYN2):c.383A>G (p.Lys128Arg)	SYN2 (K128R)	Single nucleotide variant (missense variant)	SYN2-related disorder	GBenign
Select item 3042477	NM_133625.6(SYN2):c.578C>T (p.Ala193Val)	SYN2 (A193V)	Single nucleotide variant (missense variant)	SYN2-related disorder	GBenign
Select item 3043360	NM_133625.6(SYN2):c.789G>T (p.Thr263=)	SYN2	Single nucleotide variant (synonymous variant)	SYN2-related disorder	GLikely benign
Select item 3029391	NM_133625.6(SYN2):c.1308+1G>A	SYN2	Single nucleotide variant (splice donor variant)	SYN2-related disorder	GUncertain significance
Select item 3050302	NM_133625.6(SYN2):c.1370-4del	SYN2	Deletion (intron variant)	SYN2-related disorder	GLikely benign
Select item 1298153	NM_133625.6(SYN2):c.1516A>G (p.Thr506Ala)	SYN2 (T506A)	Single nucleotide variant (missense variant)	SYN2-related disorder +1 more	GBenign
Select item 3053612	NM_133625.6(SYN2):c.1620G>A (p.Ser540=)	SYN2	Single nucleotide variant (synonymous variant)	SYN2-related disorder	GBenign
Select item 3059730	NM_133625.6(SYN2):c.1698A>G (p.Ala566=)	SYN2	Single nucleotide variant (synonymous variant)	SYN2-related disorder	GBenign

ClinVar