ClinVar Miner

Submissions for variant NM_019844.4(SLCO1B3):c.67C>T (p.Arg23Cys)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Revvity Omics, Revvity RCV003136851 SCV003823897 uncertain significance Rotor syndrome 2022-01-18 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV003136851 SCV004565061 uncertain significance Rotor syndrome 2023-03-29 criteria provided, single submitter clinical testing

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