List of variants in gene UNC13D reported as likely pathogenic by GeneDx

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_199242.3(UNC13D):c.919C>T (p.Gln307Ter)	rs747169857	0.00001
NM_199242.3(UNC13D):c.1241G>T (p.Arg414Leu)	rs768171054
NM_199242.3(UNC13D):c.1820G>C (p.Arg607Pro)	rs377293829
NM_199242.3(UNC13D):c.869C>A (p.Ser290Ter)	rs202020396

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