ClinVar Miner

Submissions for variant NM_000371.4(TTR):c.54T>C (p.Ser18=)

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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 RCV002582267 SCV003492757 likely benign Amyloidosis, hereditary systemic 1 2023-10-27 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV005239663 SCV005884335 likely benign not specified 2024-12-02 criteria provided, single submitter clinical testing

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