ClinVar Miner

Submissions for variant NM_012452.3(TNFRSF13B):c.519C>T (p.Ala173=)

gnomAD frequency: 0.00061  dbSNP: rs151139237
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 RCV000648149 SCV000769963 likely benign Immunodeficiency, common variable, 2 2024-12-17 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004704163 SCV005212253 likely benign not provided criteria provided, single submitter not provided

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