ClinVar Miner

Submissions for variant NM_000769.1(CYP2C19):c.358T>C (p.Trp120Arg)

gnomAD frequency: 0.00159  dbSNP: rs41291556
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Clinical Pharmacogenetics Implementation Consortium RCV000783659 SCV000922182 drug response CYP2C19: no function practice guideline curation
Eurofins Ntd Llc (ga) RCV000394401 SCV000338707 other not provided 2015-12-28 criteria provided, single submitter clinical testing

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