ClinVar Miner

Submissions for variant NM_000548.5(TSC2):c.3258G>A (p.Gly1086=)

dbSNP: rs2151440552
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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 RCV001394253 SCV001595935 likely benign Tuberous sclerosis 2 2023-10-10 criteria provided, single submitter clinical testing

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