ClinVar Miner

Submissions for variant NM_019844.4(SLCO1B3):c.683C>A (p.Ser228Tyr)

gnomAD frequency: 0.00001  dbSNP: rs760497665
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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 RCV001287540 SCV001474239 uncertain significance Rotor syndrome 2020-05-08 criteria provided, single submitter clinical testing

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