ClinVar Miner

Submissions for variant NM_182918.4(ERG):c.657G>A (p.Met219Ile)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Diagnostics Laboratory, National Institute of Medical Genomics RCV003444132 SCV004036061 uncertain significance Acute lymphoid leukemia 2023-09-23 criteria provided, single submitter clinical testing

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