ClinVar Miner

List of variants in gene UNC13D reported as uncertain significance by Department of Pathology and Laboratory Medicine, Sinai Health System

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_199242.3(UNC13D):c.2191G>A (p.Val731Met)	rs377549461	0.00012
NM_199242.3(UNC13D):c.5C>T (p.Ala2Val)	rs752295384	0.00003

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