"PreventionGenetics, part of Exact Sciences"[submitter] AND "RAB28"[ge - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3035465	NM_001017979.3(RAB28):c.574-3173G>A	RAB28	Single nucleotide variant (3 prime UTR variant +1 more)	RAB28-related disorder	GBenign
Select item 3043569	NM_001017979.3(RAB28):c.-9C>T	RAB28, LOC111828517	Single nucleotide variant (5 prime UTR variant)	RAB28-related disorder	GLikely benign