ClinVar Miner

Submissions for variant NM_052945.4(TNFRSF13C):c.195G>A (p.Ala65=)

gnomAD frequency: 0.00001  dbSNP: rs1408228920
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 RCV002176341 SCV002474168 likely benign Immunodeficiency, common variable, 4 2023-04-20 criteria provided, single submitter clinical testing

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