ClinVar Miner

Submissions for variant NM_003200.5(TCF3):c.1806G>A (p.Leu602=)

dbSNP: rs1376446279
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001002629 SCV001160612 likely benign Agammaglobulinemia 8, autosomal dominant 2019-06-08 criteria provided, single submitter clinical testing
Invitae RCV003769389 SCV004644245 likely benign not provided 2023-05-07 criteria provided, single submitter clinical testing

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