"PreventionGenetics, part of Exact Sciences"[submitter] AND "RXRB"[gen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 779906	NM_021976.5(RXRB):c.1455-10_1455-5dup	RXRB	Duplication (intron variant)	not provided +1 more	GBenign
Select item 3041645	NM_021976.5(RXRB):c.1419C>G (p.Thr473=)	RXRB	Single nucleotide variant (synonymous variant)	RXRB-related disorder	GLikely benign
Select item 3049286	NM_021976.5(RXRB):c.1206C>T (p.His402=)	RXRB	Single nucleotide variant (synonymous variant)	RXRB-related disorder	GLikely benign
Select item 3050300	NM_021976.5(RXRB):c.1194C>T (p.Ala398=)	RXRB	Single nucleotide variant (synonymous variant)	RXRB-related disorder	GLikely benign
Select item 1254260	NM_021976.5(RXRB):c.1152C>T (p.Phe384=)	RXRB	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 3034436	NM_021976.5(RXRB):c.641-6C>G	RXRB	Single nucleotide variant (intron variant)	RXRB-related disorder	GBenign
Select item 3042895	NM_021976.5(RXRB):c.624C>T (p.Cys208=)	RXRB	Single nucleotide variant (synonymous variant)	RXRB-related disorder	GBenign
Select item 3061577	NM_021976.5(RXRB):c.310C>T (p.Pro104Ser)	RXRB (P104S)	Single nucleotide variant (missense variant +1 more)	RXRB-related disorder	GLikely benign
Select item 3042026	NM_001291989.2(RXRB):c.16+9A>C	RXRB	Single nucleotide variant (intron variant)	RXRB-related disorder	GLikely benign

ClinVar