ClinVar Miner

Submissions for variant NM_000365.6(TPI1):c.457+7C>G

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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 RCV003547076 SCV004251248 likely benign not provided 2023-12-01 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV003626878 SCV004562675 likely benign Triosephosphate isomerase deficiency 2023-10-13 criteria provided, single submitter clinical testing

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