ClinVar Miner

Submissions for variant NM_000312.4(PROC):c.92A>T (p.Glu31Val)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center For Human Genetics And Laboratory Diagnostics, Dr. Klein, Dr. Rost And Colleagues RCV002776555 SCV003035435 uncertain significance Thrombophilia due to protein C deficiency, autosomal dominant 2022-06-20 criteria provided, single submitter clinical testing

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