List of variants in gene UNC13D reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_199242.3(UNC13D):c.1131C>G (p.Ser377Arg)	rs142335129	0.00016
NM_199242.3(UNC13D):c.670C>T (p.His224Tyr)	rs145607492	0.00014
NM_199242.3(UNC13D):c.2191G>A (p.Val731Met)	rs377549461	0.00012
NM_199242.3(UNC13D):c.2219C>T (p.Thr740Met)	rs761013333	0.00006
NM_199242.3(UNC13D):c.71G>A (p.Arg24His)	rs777619516	0.00006
NM_199242.3(UNC13D):c.2091+2_2091+3dup	rs778809705	0.00001
NM_199242.3(UNC13D):c.248G>A (p.Arg83Gln)	rs143944122	0.00001
NM_199242.3(UNC13D):c.2206C>A (p.Gln736Lys)	rs1187815814
NM_199242.3(UNC13D):c.3224G>T (p.Arg1075Leu)	rs377594755

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