ClinVar Miner

Submissions for variant CYP2C19*16

gnomAD frequency: 0.00010  dbSNP: rs192154563
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Clinical Pharmacogenetics Implementation Consortium RCV000782430 SCV000920953 drug response CYP2C19: decreased function practice guideline curation

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