ClinVar Miner

Submissions for variant NM_000767.5(CYP2B6):c.637T>C (p.Phe213Leu)

gnomAD frequency: 0.00002  dbSNP: rs371424910
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000106298 SCV000143757 drug response Efavirenz response 2013-05-01 no assertion criteria provided literature only

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