ClinVar Miner

Submissions for variant NM_000365.6(TPI1):c.463G>A (p.Val155Met)

gnomAD frequency: 0.00118  dbSNP: rs188138723
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV002248909 SCV002516109 uncertain significance not specified 2022-05-04 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003094007 SCV003441196 benign not provided 2023-02-02 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV003138122 SCV003827847 uncertain significance Triosephosphate isomerase deficiency 2023-01-09 criteria provided, single submitter clinical testing

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