ClinVar Miner

Submissions for variant NM_001994.3(F13B):c.1079T>A (p.Val360Glu)

dbSNP: rs2125068039
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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 RCV002222124 SCV002499564 uncertain significance Factor XIII, b subunit, deficiency of criteria provided, single submitter clinical testing

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