ClinVar Miner

Submissions for variant CYP2C19*15 (rs17882687)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Clinical Pharmacogenetics Implementation Consortium RCV000783650 SCV000922173 drug response CYP2C19: normal function practice guideline curation
Invitae RCV000893758 SCV001037714 benign not provided 2018-05-17 criteria provided, single submitter clinical testing

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