ClinVar Miner

Submissions for variant NM_001561.6(TNFRSF9):c.166G>A (p.Ala56Thr)

gnomAD frequency: 0.00332  dbSNP: rs9657963
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Diagnostic Laboratory, Division of Genomic Diagnostics, Children's Hospital of Philadelphia RCV000238983 SCV000297102 benign not specified 2015-11-20 criteria provided, single submitter clinical testing
Invitae RCV001521632 SCV001731008 benign not provided 2024-01-31 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV000238983 SCV002067253 likely benign not specified 2021-06-22 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV001521632 SCV004128126 likely benign not provided 2024-06-01 criteria provided, single submitter clinical testing TNFRSF9: BP4, BS2

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