List of variants in gene UNC13D reported as likely benign for not specified

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: 27

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HGVS	dbSNP	gnomAD frequency
NM_199242.3(UNC13D):c.2599A>G (p.Lys867Glu)	rs1135688	0.47045
NM_199242.3(UNC13D):c.1579C>T (p.Arg527Trp)	rs75366116	0.01644
NM_199242.3(UNC13D):c.175G>A (p.Ala59Thr)	rs9904366	0.01403
NM_199242.3(UNC13D):c.753+3G>A	rs116229331	0.00627
NM_199242.3(UNC13D):c.1055+47C>T	rs185419295	0.00566
NM_199242.3(UNC13D):c.754-49G>A	rs201702634	0.00387
NM_199242.3(UNC13D):c.684-31C>T	rs114861309	0.00363
NM_199242.3(UNC13D):c.2335G>A (p.Val779Met)	rs113861754	0.00355
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.2341G>A (p.Val781Ile)	rs149871493	0.00162
NM_199242.3(UNC13D):c.227C>T (p.Thr76Met)	rs78028658	0.00153
NM_199242.3(UNC13D):c.2052C>G (p.Leu684=)	rs150861045	0.00070
NM_199242.3(UNC13D):c.3078C>T (p.Pro1026=)	rs372034111	0.00056
NM_199242.3(UNC13D):c.2625+38G>A	rs199759320	0.00048
NM_199242.3(UNC13D):c.1228A>C (p.Ile410Leu)	rs117221419	0.00040
NM_199242.3(UNC13D):c.972C>T (p.Asp324=)	rs368990813	0.00029
NM_199242.3(UNC13D):c.811C>T (p.Pro271Ser)	rs139564938	0.00020
NM_199242.3(UNC13D):c.114G>A (p.Pro38=)	rs755103812	0.00019
NM_199242.3(UNC13D):c.1212C>G (p.Thr404=)	rs201727463	0.00017
NM_199242.3(UNC13D):c.262-7C>T	rs368236546	0.00017
NM_199242.3(UNC13D):c.1626G>A (p.Thr542=)	rs371924071	0.00010
NM_199242.3(UNC13D):c.273G>A (p.Val91=)	rs149494974	0.00007
NM_199242.3(UNC13D):c.1611G>A (p.Val537=)	rs538427767	0.00001
NM_199242.3(UNC13D):c.594G>A (p.Ala198=)	rs755967157	0.00001
NM_199242.3(UNC13D):c.1447-14C>T
NM_199242.3(UNC13D):c.2340C>G (p.Gly780=)	rs556654678

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