List of variants in gene combination LOC130061690, UNC13D reported as uncertain significance for immune system disorder

Minimum submission review status:		Collection method:
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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: 4

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HGVS	dbSNP	gnomAD frequency
NM_199242.2(UNC13D):c.-332G>A	rs560759175	0.00059
NM_199242.2(UNC13D):c.-363C>T	rs886053429	0.00044
NM_199242.2(UNC13D):c.-347G>A	rs534324377	0.00031
NM_199242.2(UNC13D):c.-328G>A	rs867915391	0.00001

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