ClinVar Miner

Submissions for variant NM_000392.5(ABCC2):c.4581C>T (p.Pro1527=) (rs1564704231)

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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 RCV000731578 SCV000859416 uncertain significance not provided 2018-01-26 criteria provided, single submitter clinical testing

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