ClinVar Miner

Submissions for variant NM_012452.3(TNFRSF13B):c.484C>T (p.Leu162=)

dbSNP: rs2087502054
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002178062 SCV002348774 likely benign Immunodeficiency, common variable, 2 2022-08-19 criteria provided, single submitter clinical testing

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