List of variants in gene VPS13B reported as uncertain significance by Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC)

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_152564.5(VPS13B):c.2471C>T (p.Ser824Phe)	rs145419141	0.00019
NM_152564.5(VPS13B):c.6530G>A (p.Arg2177His)	rs147099791	0.00016
NM_152564.5(VPS13B):c.5902T>C (p.Cys1968Arg)	rs1422533086	0.00001
NM_152564.5(VPS13B):c.11967_11970dup (p.Ala3991Ter)	rs769983613

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