ClinVar Miner

Submissions for variant NM_000548.5(TSC2):c.1258-8T>G

dbSNP: rs1175574879
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001463616 SCV001667563 likely benign Tuberous sclerosis 2 2022-12-24 criteria provided, single submitter clinical testing
Institute for Clinical Genetics, University Hospital TU Dresden, University Hospital TU Dresden RCV003238255 SCV002011356 uncertain significance not provided 2021-11-03 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001463616 SCV002041143 likely benign Tuberous sclerosis 2 2021-11-07 criteria provided, single submitter clinical testing

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