ClinVar Miner

Submissions for variant NM_001348800.3(ZBTB20):c.598G>T (p.Val200Leu)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Neuberg Centre For Genomic Medicine, NCGM RCV003445314 SCV004171851 uncertain significance Primrose syndrome criteria provided, single submitter clinical testing

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