Related gene-specific medical variations for Gene (Select 5915) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3360252	NM_000965.5(RARB):c.1121T>C (p.Ile374Thr)	RARB (I262T +5 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3360039	NM_000965.5(RARB):c.1086C>A (p.Ser362Arg)	RARB (S250R +5 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 814429	GRCh37/hg19 3p24.2(chr3:25329791-25554978)x3	RARB	Copy number gain	not provided	GUncertain significance

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