List of variants in gene RAB28 reported as likely pathogenic for not provided

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_001017979.3(RAB28):c.76-9A>G	rs372774679	0.00002
NM_004249.4(RAB28):c.651T>G (p.Cys217Trp)	rs751163782	0.00001
NM_004249.4(RAB28):c.574-1G>A

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