ClinVar Miner

Submissions for variant CYP2C19*11

gnomAD frequency: 0.00302  dbSNP: rs58973490
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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 RCV000782426 SCV000920949 drug response CYP2C19: normal function practice guideline curation
CeGaT Center for Human Genetics Tuebingen RCV003884727 SCV004700231 likely benign not provided 2024-01-01 criteria provided, single submitter clinical testing CYP2C19: BP4, BS2

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