ClinVar Miner

Submissions for variant NM_000548.5(TSC2):c.5161-17C>G

dbSNP: rs1256554136
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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 RCV003627762 SCV004405055 likely benign Tuberous sclerosis 2 2023-03-04 criteria provided, single submitter clinical testing

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