ClinVar Miner

Submissions for variant NM_001206999.2(CIT):c.3157-37del

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV003392076 SCV004132083 likely benign not provided 2023-06-01 criteria provided, single submitter clinical testing CIT: BS2

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