ClinVar Miner

Submissions for variant NM_000128.4(F11):c.1469T>C (p.Val490Ala)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Revvity Omics, Revvity RCV003147148 SCV003832319 uncertain significance Hereditary factor XI deficiency disease 2021-12-09 criteria provided, single submitter clinical testing

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