"PreventionGenetics, part of Exact Sciences"[submitter] AND "RAB11B-AS - ClinVar - NCBI

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Items: 3

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1904841	NM_004218.4(RAB11B):c.33A>G (p.Leu11=)	RAB11B, RAB11B-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	RAB11B-related disorder +1 more	GLikely benign
Select item 781382	NM_004218.4(RAB11B):c.40+6G>T	RAB11B, RAB11B-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided +1 more	GBenign
Select item 1610479	NM_004218.4(RAB11B):c.40+7C>T	RAB11B, RAB11B-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided +1 more	GBenign/Likely benign

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