ClinVar Miner

Submissions for variant NM_021871.4(FGA):c.1838A>G (p.His613Arg) (rs201686865)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000323812 SCV000447807 likely benign Familial visceral amyloidosis, Ostertag type 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000381748 SCV000447808 likely benign Afibrinogenemia, congenital 2016-06-14 criteria provided, single submitter clinical testing

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