ClinVar Miner

Submissions for variant NM_021870.2(FGG):c.902G>A (p.Arg301His) (rs121913088)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
NIHR Bioresource Rare Diseases, University of Cambridge RCV000851952 SCV000899374 pathogenic Hypofibrinogenemia 2019-02-01 criteria provided, single submitter research
OMIM RCV000017777 SCV000038056 other FIBRINOGEN HAIFA 1 2014-09-19 no assertion criteria provided literature only

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