List of variants in gene SYT14 reported as benign for cerebellar ataxia

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001146262.4(SYT14):c.1419T>C (p.Tyr473=)	rs17188183	0.09972
NM_001146262.4(SYT14):c.672AGA[1] (p.Glu225del)	rs2307890

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