List of variants in gene VPS13B reported by St. Jude Molecular Pathology, St. Jude Children's Research Hospital

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_152564.5(VPS13B):c.2704A>G (p.Lys902Glu)	rs149531438	0.00074
NM_152564.5(VPS13B):c.1627A>G (p.Thr543Ala)	rs372625091	0.00004
NM_152564.5(VPS13B):c.8639C>T (p.Ser2880Leu)	rs760166376	0.00002
NM_152564.5(VPS13B):c.10384C>T (p.Leu3462Phe)	rs761972356	0.00001
NM_152564.5(VPS13B):c.11197C>A (p.Leu3733Met)	rs1318142770	0.00001
NM_152564.5(VPS13B):c.328C>T (p.Arg110Cys)	rs368290618	0.00001

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