List of variants in gene VPS13D reported as likely benign for cerebellar ataxia

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_015378.4(VPS13D):c.5334T>A (p.Ser1778Arg)	rs144311414	0.00133
NM_015378.4(VPS13D):c.1114G>A (p.Glu372Lys)	rs76782506	0.00112

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