ClinVar Miner

Submissions for variant NM_000548.5(TSC2):c.139-20C>A

gnomAD frequency: 0.00001  dbSNP: rs779808076
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002638033 SCV003517273 likely benign Tuberous sclerosis 2 2022-04-09 criteria provided, single submitter clinical testing

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