List of variants in gene UNC13D reported as benign by Illumina Laboratory Services, Illumina

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: 20

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HGVS	dbSNP	gnomAD frequency
NM_199242.3(UNC13D):c.3198A>G (p.Glu1066=)	rs7210574	0.49757
NM_199242.3(UNC13D):c.2599A>G (p.Lys867Glu)	rs1135688	0.47045
NM_199242.3(UNC13D):c.1992+5G>A	rs17581728	0.19407
NM_199242.3(UNC13D):c.*326C>T	rs9916685	0.08635
NM_199242.2(UNC13D):c.-149G>A	rs3744012	0.07109
NM_199242.3(UNC13D):c.1744C>T (p.Leu582=)	rs75853379	0.02622
NM_199242.3(UNC13D):c.1977C>T (p.Thr659=)	rs2290770	0.02469
NM_199242.2(UNC13D):c.-250C>T	rs57161046	0.02092
NM_199242.2(UNC13D):c.-260C>T	rs113482537	0.01892
NM_199242.3(UNC13D):c.951+13T>G	rs140758914	0.01637
NM_199242.3(UNC13D):c.3252T>C (p.His1084=)	rs61753922	0.01313
NM_199242.3(UNC13D):c.1992+11T>C	rs112501965	0.01262
NM_199242.3(UNC13D):c.904C>T (p.Leu302Phe)	rs55661958	0.01066
NM_199242.3(UNC13D):c.*658G>A	rs115709152	0.01012
NM_199242.2(UNC13D):c.-180C>T	rs149878313	0.00936
NM_199242.3(UNC13D):c.847A>G (p.Ile283Val)	rs61754871	0.00194
NM_199242.3(UNC13D):c.1056-13C>T	rs141030299	0.00169
NM_199242.3(UNC13D):c.2448-8dup	rs3217698
NM_199242.3(UNC13D):c.279C>T (p.Pro93=)	rs3744007
NM_199242.3(UNC13D):c.888G>C (p.Pro296=)	rs7223416

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