ClinVar Miner

Submissions for variant NM_001994.3(F13B):c.1739-8_1739-6del

dbSNP: rs556380704
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000362196 SCV000352590 uncertain significance Factor XIII, b subunit, deficiency of 2016-06-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000881320 SCV001024481 likely benign not provided 2019-12-31 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000881320 SCV002496970 likely benign not provided 2022-03-01 criteria provided, single submitter clinical testing F13B: BP4

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