ClinVar Miner

List of variants in gene VPS13B reported as uncertain significance by Neuberg Centre For Genomic Medicine, NCGM

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.11438A>G (p.His3813Arg)	rs549702100	0.00002
NM_152564.5(VPS13B):c.8423A>T (p.Asn2808Ile)	rs368357351

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