ClinVar Miner

Submissions for variant NM_000548.5(TSC2):c.807C>A (p.Gly269=)

dbSNP: rs1297815371
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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 RCV001394052 SCV001595732 likely benign Tuberous sclerosis 2 2022-02-03 criteria provided, single submitter clinical testing

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