ClinVar Miner

Submissions for variant NM_021871.4(FGA):c.1631C>T (p.Thr544Ile)

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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 RCV005037509 SCV005660606 uncertain significance Familial visceral amyloidosis, Ostertag type; Congenital afibrinogenemia; Familial dysfibrinogenemia 2024-01-22 criteria provided, single submitter clinical testing

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