ClinVar Miner

Submissions for variant NM_012452.3(TNFRSF13B):c.465G>A (p.Leu155=)

dbSNP: rs2143642450
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002101503 SCV002433433 likely benign Immunodeficiency, common variable, 2 2024-02-24 criteria provided, single submitter clinical testing

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