ClinVar Miner

Submissions for variant NM_000548.5(TSC2):c.3884-8C>T

dbSNP: rs397515219
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001454744 SCV001658482 likely benign Tuberous sclerosis 2 2024-07-12 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV000055521 SCV004825325 likely benign Tuberous sclerosis syndrome 2024-09-27 criteria provided, single submitter clinical testing
Tuberous sclerosis database (TSC2) RCV000055521 SCV000083744 not provided Tuberous sclerosis syndrome no assertion provided curation

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