List of variants in gene UNC13D reported as pathogenic by Department of Pathology and Laboratory Medicine, Sinai Health System

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_199242.3(UNC13D):c.1389+1G>A	rs777759523	0.00006
NM_199242.3(UNC13D):c.817C>T (p.Arg273Ter)	rs201589664	0.00001
NM_199242.3(UNC13D):c.2346_2349del (p.Arg782fs)	rs764196809

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