ClinVar Miner

Submissions for variant NM_000110.3(DPYD):c.496A>G (p.Met166Val) (rs2297595)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics Inc RCV000086499 SCV000841883 benign not provided 2017-04-20 criteria provided, single submitter clinical testing
Diasio Lab, Mayo Clinic RCV000086499 SCV000118665 not provided not provided no assertion provided not provided
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000245015 SCV000345079 benign not specified 2016-08-29 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000276917 SCV000359607 likely benign Dihydropyrimidine dehydrogenase deficiency 2016-06-14 criteria provided, single submitter clinical testing
PreventionGenetics RCV000245015 SCV000302305 benign not specified criteria provided, single submitter clinical testing

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