ClinVar Miner

Submissions for variant NM_000106.6(CYP2D6):c.368G>T (p.Arg123Leu)

gnomAD frequency: 0.00010  dbSNP: rs373000587
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics RCV000162081 SCV000212080 drug-response not provided no assertion criteria provided not provided Converted during submission to drug response.

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