ClinVar Miner

Submissions for variant NM_001080522.2(CC2D2A):c.2061G>A (p.Leu687=) (rs182372139)

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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 RCV000598244 SCV000707673 uncertain significance not provided 2017-04-10 criteria provided, single submitter clinical testing

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