ClinVar Miner

Submissions for variant NM_000392.5(ABCC2):c.3424G>C (p.Val1142Leu) (rs375280444)

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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 RCV000595615 SCV000704007 uncertain significance not provided 2016-11-22 criteria provided, single submitter clinical testing

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