ClinVar Miner

Submissions for variant NM_002972.4(SBF1):c.898-4G>A (rs377428323)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Praxis fuer Humangenetik Tuebingen RCV000416032 SCV000493537 uncertain significance not provided 2017-01-01 criteria provided, single submitter clinical testing
Invitae RCV000416032 SCV001044341 likely benign not provided 2019-12-31 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001000978 SCV001158079 likely benign Charcot-Marie-Tooth disease, type 4B3 2019-04-25 criteria provided, single submitter clinical testing

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