List of variants in gene VPS13B reported as uncertain significance by Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics

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.11158G>A (p.Glu3720Lys)	rs150393340	0.00110
NM_152564.5(VPS13B):c.11180G>A (p.Arg3727Gln)	rs913075497	0.00001
NM_152564.5(VPS13B):c.11745+4C>T	rs751045565	0.00001
NM_152564.5(VPS13B):c.5087T>C (p.Val1696Ala)	rs878852995	0.00001

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