ClinVar Miner

Submissions for variant NM_021871.4(FGA):c.531C>G (p.Ile177Met)

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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 RCV005027263 SCV005658167 uncertain significance Familial visceral amyloidosis, Ostertag type; Congenital afibrinogenemia; Familial dysfibrinogenemia 2024-02-04 criteria provided, single submitter clinical testing

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