ClinVar Miner

Submissions for variant CYP2C19*10/*10

gnomAD frequency: 0.00100  dbSNP: rs6413438
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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 RCV000783543 SCV000922066 drug response Voriconazole response practice guideline curation
Clinical Pharmacogenetics Implementation Consortium RCV000783797 SCV000922320 drug response Citalopram response practice guideline curation
Clinical Pharmacogenetics Implementation Consortium RCV000783798 SCV000922321 drug response Escitalopram response practice guideline curation
Clinical Pharmacogenetics Implementation Consortium RCV000784299 SCV000922822 drug response Sertraline response practice guideline curation

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