ClinVar Miner

Submissions for variant NM_000110.4(DPYD):c.2622+1G>A

dbSNP: rs1057517095
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000410613 SCV000486740 likely pathogenic Dihydropyrimidine dehydrogenase deficiency 2016-07-29 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV000410613 SCV000894210 likely pathogenic Dihydropyrimidine dehydrogenase deficiency 2018-10-31 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV000410613 SCV004049521 likely pathogenic Dihydropyrimidine dehydrogenase deficiency 2023-04-11 criteria provided, single submitter clinical testing
Baylor Genetics RCV000410613 SCV004194131 likely pathogenic Dihydropyrimidine dehydrogenase deficiency 2023-01-27 criteria provided, single submitter clinical testing

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