ClinVar Miner

Submissions for variant NM_021870.3(FGG):c.1030G>C (p.Asp344His)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetics and Molecular Pathology, SA Pathology RCV003447705 SCV004175332 likely pathogenic Familial dysfibrinogenemia 2021-07-16 criteria provided, single submitter clinical testing

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