ClinVar Miner

Submissions for variant NM_052945.4(TNFRSF13C):c.367+14G>C

gnomAD frequency: 0.00001  dbSNP: rs781263826
Minimum review status: Collection method:
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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 RCV002090716 SCV002372692 likely benign Immunodeficiency, common variable, 4 2022-07-11 criteria provided, single submitter clinical testing

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