ClinVar Miner

Submissions for variant NM_021871.4(FGA):c.991A>G (p.Thr331Ala) (rs6050)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000338448 SCV000447819 benign Afibrinogenemia, congenital 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000405212 SCV000447820 benign Familial visceral amyloidosis, Ostertag type 2016-06-14 criteria provided, single submitter clinical testing
OMIM RCV000017882 SCV000038161 risk factor Venous thromboembolism, susceptibility to 2006-03-01 no assertion criteria provided literature only
PreventionGenetics RCV000246757 SCV000304604 benign not specified criteria provided, single submitter clinical testing

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