ClinVar Miner

Submissions for variant CYP2C19*8 (rs41291556)

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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 RCV000783659 SCV000922182 drug response CYP2C19: no function practice guideline curation
EGL Genetic Diagnostics, Eurofins Clinical Diagnostics RCV000394401 SCV000338707 other not provided 2015-12-28 criteria provided, single submitter clinical testing

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