ClinVar Miner

Submissions for variant NM_021871.4(FGA):c.696G>T (p.Leu232Phe)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV005037515 SCV005658159 uncertain significance Familial visceral amyloidosis, Ostertag type; Congenital afibrinogenemia; Familial dysfibrinogenemia 2024-02-19 criteria provided, single submitter clinical testing

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