List of variants in gene UNC13D reported as likely 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_199242.3(UNC13D):c.1579C>T (p.Arg527Trp)	rs75366116	0.01644
NM_199242.3(UNC13D):c.*64C>T	rs113904350	0.00793
NM_199242.3(UNC13D):c.2298+15C>T	rs112341334	0.00741
NM_199242.3(UNC13D):c.2955-14G>C	rs138462345	0.00196
NM_199242.3(UNC13D):c.610A>G (p.Met204Val)	rs144722609	0.00081
NM_199242.3(UNC13D):c.2052C>G (p.Leu684=)	rs150861045	0.00070
NM_199242.3(UNC13D):c.1228A>C (p.Ile410Leu)	rs117221419	0.00040
NM_199242.3(UNC13D):c.154-8T>A	rs369433391	0.00009

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