ClinVar Miner

Submissions for variant NM_019844.4(SLCO1B3):c.1732G>C (p.Val578Leu)

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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 RCV003643518 SCV004562548 uncertain significance Rotor syndrome 2023-09-21 criteria provided, single submitter clinical testing

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