ClinVar Miner

Submissions for variant NM_001394998.1(TANC2):c.2582+8A>G

gnomAD frequency: 0.00261  dbSNP: rs138001880
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000970026 SCV001117580 benign not provided 2018-06-04 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000970026 SCV002545964 likely benign not provided 2023-08-01 criteria provided, single submitter clinical testing TANC2: BP4, BS1

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