ClinVar Miner

Submissions for variant CYP2C19*13/*13

gnomAD frequency: 0.00505  dbSNP: rs17879685
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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 RCV000782477 SCV000921000 drug response Citalopram response practice guideline curation
Clinical Pharmacogenetics Implementation Consortium RCV000782478 SCV000921001 drug response Escitalopram response practice guideline curation
Clinical Pharmacogenetics Implementation Consortium RCV000783063 SCV000921586 drug response Sertraline response practice guideline curation
Clinical Pharmacogenetics Implementation Consortium RCV000783610 SCV000922133 drug response Voriconazole response practice guideline curation

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