ClinVar Miner

Submissions for variant NM_000110.4(DPYD):c.1178del (p.Pro393fs)

dbSNP: rs1553197926
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000674165 SCV000799452 likely pathogenic Dihydropyrimidine dehydrogenase deficiency 2018-04-18 criteria provided, single submitter clinical testing
Baylor Genetics RCV000674165 SCV005060248 likely pathogenic Dihydropyrimidine dehydrogenase deficiency 2023-12-05 criteria provided, single submitter clinical testing

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