ClinVar Miner

Submissions for variant NM_002087.3(GRN):c.359C>A (p.Ser120Tyr) (rs63750043)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000084437 SCV000652428 likely benign not provided 2019-02-04 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000084437 SCV000843037 benign not provided 2017-10-09 criteria provided, single submitter clinical testing
VIB Department of Molecular Genetics, University of Antwerp RCV000084437 SCV000116573 not provided not provided no assertion provided not provided
Mayo Clinic Genetic Testing Laboratories,Mayo Clinic RCV000084437 SCV000801381 uncertain significance not provided 2017-11-03 no assertion criteria provided clinical testing

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