ClinVar Miner

Submissions for variant NM_012452.3(TNFRSF13B):c.489C>A (p.Val163=)

dbSNP: rs2143642351
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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 RCV002103822 SCV002391025 likely benign Immunodeficiency, common variable, 2 2022-06-09 criteria provided, single submitter clinical testing

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