ClinVar Miner

Submissions for variant NM_000062.3(SERPING1):c.1475T>C (p.Met492Thr)

dbSNP: rs978962357
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, University of Wuerzburg RCV000490705 SCV000579342 likely pathogenic Angioedema no assertion criteria provided clinical testing

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