ClinVar Miner

Submissions for variant NM_000548.5(TSC2):c.5259+7A>G

dbSNP: rs1060504122
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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 RCV000464126 SCV000556686 likely benign Tuberous sclerosis 2 2024-11-11 criteria provided, single submitter clinical testing

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