ClinVar Miner

List of variants in gene VPS13B reported as likely pathogenic by Institute of Human Genetics, University of Leipzig Medical Center

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_152564.5(VPS13B):c.2591C>A (p.Ser864Ter)	rs140936527	0.00001
NM_152564.5(VPS13B):c.2828del (p.Ala943fs)	rs1554765140

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