"Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, E - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1284586	NM_006446.5(SLCO1B1):c.210C>T (p.Asp70=)	SLCO1B1	Single nucleotide variant (synonymous variant)	Rotor syndrome	GLikely benign
Select item 307939	NM_006446.5(SLCO1B1):c.633A>G (p.Ile211Met)	SLCO1B1 (I211M)	Single nucleotide variant (missense variant)	Rotor syndrome	GLikely benign
Select item 307950	NM_006446.5(SLCO1B1):c.1331+9A>G	SLCO1B1	Single nucleotide variant (intron variant)	Rotor syndrome	GConflicting classifications of pathogenicity

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