ClinVar Miner

Submissions for variant NM_000110.4(DPYD):c.1316del (p.Gly439fs)

dbSNP: rs1057516761
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000411796 SCV000486183 likely pathogenic Dihydropyrimidine dehydrogenase deficiency 2016-04-12 criteria provided, single submitter clinical testing
Baylor Genetics RCV000411796 SCV005060236 likely pathogenic Dihydropyrimidine dehydrogenase deficiency 2024-02-27 criteria provided, single submitter clinical testing

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