List of variants in gene UNC13D reported as uncertain significance 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: 14

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HGVS	dbSNP	gnomAD frequency
NM_199242.3(UNC13D):c.2341G>A (p.Val781Ile)	rs149871493	0.00162
NM_199242.3(UNC13D):c.227C>T (p.Thr76Met)	rs78028658	0.00153
NM_199242.3(UNC13D):c.2983G>C (p.Ala995Pro)	rs138760432	0.00105
NM_199242.3(UNC13D):c.610A>G (p.Met204Val)	rs144722609	0.00081
NM_199242.3(UNC13D):c.1759C>T (p.Arg587Cys)	rs148574729	0.00021
NM_199242.3(UNC13D):c.2243C>T (p.Ala748Val)	rs375724532	0.00008
NM_199242.3(UNC13D):c.898G>A (p.Val300Met)	rs141499220	0.00005
NM_199242.3(UNC13D):c.755A>T (p.Asp252Val)	rs1131691264	0.00002
NM_199242.3(UNC13D):c.2038C>T (p.Arg680Trp)	rs200341276	0.00001
NM_199242.3(UNC13D):c.3034G>A (p.Asp1012Asn)	rs1240859315	0.00001
NM_199242.3(UNC13D):c.47G>A (p.Arg16His)	rs149195431	0.00001
NM_199242.3(UNC13D):c.1820G>C (p.Arg607Pro)	rs377293829
NM_199242.3(UNC13D):c.753+5G>A	rs1463088201
NM_199242.3(UNC13D):c.98C>T (p.Pro33Leu)	rs140437526

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