ClinVar Miner

Submissions for variant NM_012452.3(TNFRSF13B):c.445+7C>T

gnomAD frequency: 0.00008  dbSNP: rs768915966
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001464456 SCV001668426 likely benign Immunodeficiency, common variable, 2 2024-11-05 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV001815557 SCV002063580 uncertain significance not provided 2021-12-01 criteria provided, single submitter clinical testing

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