ClinVar Miner

Submissions for variant NM_012452.3(TNFRSF13B):c.690C>T (p.Cys230=)

gnomAD frequency: 0.00002  dbSNP: rs746878754
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001433691 SCV001636485 likely benign Immunodeficiency, common variable, 2 2022-07-11 criteria provided, single submitter clinical testing

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