ClinVar Miner

Submissions for variant NM_000548.5(TSC2):c.804G>A (p.Leu268=)

dbSNP: rs2151087245
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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 RCV001372332 SCV001568963 likely benign Tuberous sclerosis 2 2024-03-04 criteria provided, single submitter clinical testing

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