List of variants in gene UNC13D reported as benign for not provided

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 21

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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.570-229A>G	rs8074963	0.47320
NM_199242.3(UNC13D):c.2599A>G (p.Lys867Glu)	rs1135688	0.47045
NM_199242.3(UNC13D):c.388+122C>T	rs3744006	0.46505
NM_199242.3(UNC13D):c.154-19G>A	rs3744009	0.24392
NM_199242.3(UNC13D):c.1596+36A>G	rs3744026	0.23763
NM_199242.3(UNC13D):c.1728-48T>C	rs3744024	0.23380
NM_199242.3(UNC13D):c.2299-46C>T	rs7212635	0.18407
NM_199242.3(UNC13D):c.569+192T>C	rs8066943	0.15273
NM_199242.3(UNC13D):c.117+30G>A	rs3744011	0.10282
NM_199242.3(UNC13D):c.1977C>T (p.Thr659=)	rs2290770	0.02469
NM_199242.3(UNC13D):c.1579C>T (p.Arg527Trp)	rs75366116	0.01644
NM_199242.3(UNC13D):c.753+3G>A	rs116229331	0.00627
NM_199242.3(UNC13D):c.847A>G (p.Ile283Val)	rs61754871	0.00194
NM_199242.3(UNC13D):c.1056-89_1056-88insGGTTCTCCACCAGGGGCCCTGGAGGA	rs142821095
NM_199242.3(UNC13D):c.279C>T (p.Pro93=)	rs3744007
NM_199242.3(UNC13D):c.570-136_570-135del	rs34691954
NM_199242.3(UNC13D):c.570-159dup	rs34691954
NM_199242.3(UNC13D):c.570-286C>G	rs8069459
NM_199242.3(UNC13D):c.570-60T>G	rs8067076
NM_199242.3(UNC13D):c.888G>C (p.Pro296=)	rs7223416

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