ClinVar Miner

Submissions for variant CYP2C19*5

gnomAD frequency: 0.00001  dbSNP: rs56337013
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Clinical Pharmacogenetics Implementation Consortium RCV000783657 SCV000922180 drug response CYP2C19: no function practice guideline curation
Eurofins NTD LLC (GA) RCV000348667 SCV000338706 other not provided 2015-12-28 criteria provided, single submitter clinical testing
OMIM RCV000018396 SCV000038678 drug response Mephenytoin, poor metabolism of 1998-04-01 no assertion criteria provided literature only

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