ClinVar Miner

Submissions for variant NM_000133.3(F9):c.391+7A>G (rs6049)

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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 RCV000377411 SCV000481880 benign Hemophilia B, Factor IX Deficiency 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000555206 SCV000647887 benign Hereditary factor IX deficiency disease; Thrombophilia, X-linked, due to factor IX defect 2017-05-23 criteria provided, single submitter clinical testing

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