ClinVar Miner

Submissions for variant NM_001355436.2(SPTB):c.1350T>C (p.Phe450=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002948574 SCV003275576 benign not provided 2024-11-11 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV002948574 SCV003799266 benign not provided 2023-07-27 criteria provided, single submitter clinical testing

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