ClinVar Miner

Submissions for variant NM_052945.4(TNFRSF13C):c.252G>A (p.Leu84=)

dbSNP: rs886057589
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000281136 SCV000438944 uncertain significance Common Variable Immune Deficiency, Recessive 2016-06-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002057810 SCV002341933 likely benign Immunodeficiency, common variable, 4 2021-03-28 criteria provided, single submitter clinical testing

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