ClinVar Miner

Submissions for variant NM_020956.2(PRX):c.*1421G>A (rs117336941)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000762017 SCV000261505 benign not provided 2019-03-04 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000576841 SCV000677429 benign Charcot-Marie-Tooth disease, demyelinating, type 4F 2017-05-23 criteria provided, single submitter clinical testing
CeGaT Praxis fuer Humangenetik Tuebingen RCV000762017 SCV000892260 uncertain significance not provided 2018-04-01 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001002219 SCV001160093 likely benign not specified 2018-10-09 criteria provided, single submitter clinical testing

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