ClinVar Miner

Submissions for variant NM_000548.5(TSC2):c.3814+14C>A

dbSNP: rs374139943
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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 RCV003511860 SCV004322036 likely benign Tuberous sclerosis 2 2023-06-02 criteria provided, single submitter clinical testing

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