ClinVar Miner

Submissions for variant CYP2C19*15/*15

gnomAD frequency: 0.00626  dbSNP: rs17882687
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Clinical Pharmacogenetics Implementation Consortium RCV000783064 SCV000921587 drug response Sertraline response practice guideline curation
Clinical Pharmacogenetics Implementation Consortium RCV000783708 SCV000922231 drug response Citalopram response practice guideline curation
Clinical Pharmacogenetics Implementation Consortium RCV000783709 SCV000922232 drug response Escitalopram response practice guideline curation
Clinical Pharmacogenetics Implementation Consortium RCV000784831 SCV000923368 drug response Voriconazole response practice guideline curation

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