ClinVar Miner

Submissions for variant NM_000128.4(F11):c.55+6T>G

dbSNP: rs1739571881
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ISTH-SSC Genomics in Thrombosis and Hemostasis, KU Leuven, Center for Molecular and Vascular Biology RCV002245405 SCV002515639 uncertain significance Hereditary factor XI deficiency disease no assertion criteria provided clinical testing

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