ClinVar Miner

Submissions for variant NM_006446.5(SLCO1B1):c.79T>C (p.Leu27=)

gnomAD frequency: 0.00001  dbSNP: rs190581845
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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 RCV001802335 SCV002050268 likely benign Rotor syndrome 2020-12-30 criteria provided, single submitter clinical testing

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