ClinVar Miner

Submissions for variant NM_000133.3(F9):c.819T>C (p.Val273=) (rs1800455)

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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 RCV000402083 SCV000481886 likely benign Hemophilia B, Factor IX Deficiency 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000531327 SCV000647888 benign not provided 2019-02-27 criteria provided, single submitter clinical testing
CeGaT Praxis fuer Humangenetik Tuebingen RCV000531327 SCV001150464 likely benign not provided 2018-10-01 criteria provided, single submitter clinical testing
OMIM RCV000011346 SCV000031578 benign FACTOR IX, DNA POLYMORPHISM 1989-09-01 no assertion criteria provided literature only

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