ClinVar Miner

Submissions for variant NM_004586.3(RPS6KA3):c.1237A>G (p.Arg413Gly) (rs765914103)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000591676 SCV000708977 uncertain significance not provided 2018-06-21 criteria provided, single submitter clinical testing
Fulgent Genetics,Fulgent Genetics RCV000764872 SCV000896028 uncertain significance Coffin-Lowry syndrome; Mental retardation, X-linked 19 2018-10-31 criteria provided, single submitter clinical testing

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