ClinVar Miner

Submissions for variant NM_000392.5(ABCC2):c.601C>T (p.Leu201=) (rs749655460)

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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 RCV000729651 SCV000857327 uncertain significance not provided 2017-10-04 criteria provided, single submitter clinical testing

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