ClinVar Miner

Submissions for variant NM_000371.4(TTR):c.200+17C>A

gnomAD frequency: 0.00001  dbSNP: rs767333203
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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 RCV002083209 SCV002371676 likely benign Amyloidosis, hereditary systemic 1 2021-05-19 criteria provided, single submitter clinical testing

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