List of variants in gene VPS13A reported as uncertain significance by Counsyl

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_033305.3(VPS13A):c.4979C>G (p.Thr1660Ser)	rs139073067	0.00011
NM_033305.3(VPS13A):c.7811G>A (p.Arg2604His)	rs762985818	0.00001
NM_033305.3(VPS13A):c.5117_5122del (p.Thr1706_Glu1707del)	rs753852395

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