ClinVar Miner

Submissions for variant NM_000301.5(PLG):c.1075A>G (p.Thr359Ala)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV005039553 SCV005668204 uncertain significance Plasminogen deficiency, type I; Angioedema, hereditary, 4 2024-05-03 criteria provided, single submitter clinical testing

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