ClinVar Miner

Submissions for variant NM_019844.4(SLCO1B3):c.560C>G (p.Pro187Arg)

gnomAD frequency: 0.00008  dbSNP: rs368572652
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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 RCV001289726 SCV001477702 uncertain significance Rotor syndrome 2020-01-06 criteria provided, single submitter clinical testing

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