ClinVar Miner

Submissions for variant NM_006446.5(SLCO1B1):c.727+33C>T

dbSNP: rs2291076
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001661226 SCV001874534 benign not provided 2021-05-16 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001810197 SCV002057281 benign Rotor syndrome 2021-07-15 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001661226 SCV005236226 benign not provided criteria provided, single submitter not provided

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