ClinVar Miner

Submissions for variant NM_006446.5(SLCO1B1):c.1812C>T (p.Thr604=)

gnomAD frequency: 0.00001  dbSNP: rs779508352
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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 RCV001802714 SCV002049775 likely benign Rotor syndrome 2023-03-15 criteria provided, single submitter clinical testing

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