ClinVar Miner

Submissions for variant NM_000371.4(TTR):c.223C>T (p.Leu75=)

dbSNP: rs2073510448
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002092272 SCV002323877 likely benign Amyloidosis, hereditary systemic 1 2023-11-13 criteria provided, single submitter clinical testing

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