ClinVar Miner

Submissions for variant NM_006446.5(SLCO1B1):c.225T>G (p.Ile75Met)

dbSNP: rs1251292787
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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 RCV001802602 SCV002049023 uncertain significance Rotor syndrome 2020-10-09 criteria provided, single submitter clinical testing

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