ClinVar Miner

Submissions for variant NM_000301.5(PLG):c.59A>C (p.Glu20Ala)

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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 RCV005039519 SCV005668142 uncertain significance Plasminogen deficiency, type I; Angioedema, hereditary, 4 2024-06-08 criteria provided, single submitter clinical testing

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