ClinVar Miner

Submissions for variant NM_000301.5(PLG):c.*45A>G

gnomAD frequency: 0.54884  dbSNP: rs6690
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001649467 SCV001863174 benign not provided 2021-06-19 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001789473 SCV002031478 benign Angioedema, hereditary, 4 2021-10-25 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001789472 SCV002031479 benign Plasminogen deficiency, type I 2021-10-25 criteria provided, single submitter clinical testing

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