ClinVar Miner

Submissions for variant NM_012452.3(TNFRSF13B):c.633T>C (p.Asp211=)

gnomAD frequency: 0.00001  dbSNP: rs199592890
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000507679 SCV000605400 likely benign not specified 2017-03-29 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001432883 SCV001635663 likely benign Immunodeficiency, common variable, 2 2024-12-31 criteria provided, single submitter clinical testing

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