ClinVar Miner

List of variants in gene UNC13D reported by Genetics and Molecular Pathology, SA Pathology

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_199242.3(UNC13D):c.2341G>A (p.Val781Ile)	rs149871493	0.00162
NM_199242.3(UNC13D):c.1556T>C (p.Ile519Thr)	rs1402195363	0.00001

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