ClinVar Miner

Submissions for variant NM_003200.5(TCF3):c.145+133G>A

gnomAD frequency: 0.18839  dbSNP: rs2302419
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001544243 SCV001763243 benign Agammaglobulinemia 8, autosomal dominant 2021-07-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004717826 SCV005310110 benign not provided criteria provided, single submitter not provided

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