ClinVar Miner

Submissions for variant NM_000392.5(ABCC2):c.4160T>C (p.Phe1387Ser) (rs1554854589)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics, Eurofins Clinical Diagnostics RCV000595039 SCV000709631 uncertain significance not provided 2017-06-28 criteria provided, single submitter clinical testing

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