ClinVar Miner

Submissions for variant CYP2C19*16/*16

gnomAD frequency: 0.00010  dbSNP: rs192154563
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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 RCV000783544 SCV000922067 drug response Voriconazole response practice guideline curation
Clinical Pharmacogenetics Implementation Consortium RCV000783819 SCV000922342 drug response Citalopram response practice guideline curation
Clinical Pharmacogenetics Implementation Consortium RCV000783820 SCV000922343 drug response Escitalopram response practice guideline curation
Clinical Pharmacogenetics Implementation Consortium RCV000784351 SCV000922874 drug response Sertraline response practice guideline curation

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