ClinVar Miner

Submissions for variant NM_000767.5(CYP2B6):c.1132C>T (p.Arg378Ter)

gnomAD frequency: 0.00013  dbSNP: rs34097093
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Microbiology; University Hospital and Univeristy of Lausanne RCV000133446 SCV000188487 drug response Efavirenz response 2006-01-01 no assertion criteria provided research

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