ClinVar Miner

Submissions for variant NM_000371.4(TTR):c.-743A>T

dbSNP: rs3794885
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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 RCV000920847 SCV001066227 benign Amyloidosis, hereditary systemic 1 2025-01-20 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002495537 SCV002796033 likely benign Hyperthyroxinemia, dystransthyretinemic; Amyloidosis, hereditary systemic 1; Carpal tunnel syndrome 1 2021-10-27 criteria provided, single submitter clinical testing

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