ClinVar Miner

Submissions for variant NM_006446.5(SLCO1B1):c.485G>A (p.Cys162Tyr)

gnomAD frequency: 0.00011  dbSNP: rs138374684
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001286059 SCV001472579 uncertain significance Rotor syndrome 2020-01-21 criteria provided, single submitter clinical testing

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