List of variants in gene VPS33A reported as likely pathogenic for bone disorder

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_022916.6(VPS33A):c.1492C>T (p.Arg498Trp)	rs767748011	0.00001
NM_022916.6(VPS33A):c.599G>C (p.Arg200Pro)	rs200032973

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