ClinVar Miner

Submissions for variant NM_000062.3(SERPING1):c.979_980delinsGTGCC (p.Ser327delinsValPro)

dbSNP: rs1945411643
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Greenwood Genetic Center Diagnostic Laboratories, Greenwood Genetic Center RCV001280757 SCV001468076 likely pathogenic not provided 2020-08-25 criteria provided, single submitter clinical testing

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