"PreventionGenetics, part of Exact Sciences"[submitter] AND "RAP1B"[ge - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3041426	NM_001010942.3(RAP1B):c.58-4dup	RAP1B	Duplication (intron variant)	RAP1B-related disorder	GLikely benign
Select item 3034954	NM_001010942.3(RAP1B):c.405A>G (p.Ala135=)	RAP1B	Single nucleotide variant (synonymous variant)	RAP1B-related disorder	GLikely benign
Select item 2635924	NM_001010942.3(RAP1B):c.468+5G>A	RAP1B	Single nucleotide variant (intron variant)	RAP1B-related disorder	GUncertain significance

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