ClinVar Miner

Submissions for variant NM_021871.4(FGA):c.614A>G (p.Glu205Gly)

dbSNP: rs886059152
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000337081 SCV000447833 uncertain significance Congenital afibrinogenemia 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000375396 SCV000447834 uncertain significance Familial visceral amyloidosis, Ostertag type 2016-06-14 criteria provided, single submitter clinical testing

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