ClinVar Miner

Submissions for variant NM_000301.5(PLG):c.435G>T (p.Glu145Asp)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Revvity Omics, Revvity RCV003135047 SCV003811177 uncertain significance not provided 2021-05-10 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV005036675 SCV005668169 uncertain significance Plasminogen deficiency, type I; Angioedema, hereditary, 4 2024-06-13 criteria provided, single submitter clinical testing

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