ClinVar Miner

Submissions for variant NM_001134407.3(GRIN2A):c.1946T>G (p.Leu649Arg)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, University of Wuerzburg RCV003228229 SCV003924391 likely pathogenic Neurodevelopmental abnormality no assertion criteria provided clinical testing

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