ClinVar Miner

Submissions for variant NM_138364.4(PRMT9):c.565G>A (p.Gly189Arg)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory of Medical Genetics (UMR_S 1112), INSERM/Strasbourg University RCV003126218 SCV002569977 pathogenic Neurodevelopmental abnormality 2022-08-02 criteria provided, single submitter research

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