List of variants in gene SYT2 reported as pathogenic for not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_177402.5(SYT2):c.1094T>C (p.Leu365Pro)	rs2149064005
NM_177402.5(SYT2):c.686_687del (p.Asp228_Phe229insTer)
NM_177402.5(SYT2):c.923C>T (p.Pro308Leu)	rs587777782

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