ClinVar Miner

Submissions for variant NM_012452.3(TNFRSF13B):c.618C>T (p.Ala206=)

gnomAD frequency: 0.00133  dbSNP: rs147846226
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 RCV000895395 SCV001039432 benign Immunodeficiency, common variable, 2 2024-12-19 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV001201259 SCV001372364 benign not specified 2020-06-11 criteria provided, single submitter clinical testing

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