ClinVar Miner

Submissions for variant NM_000548.5(TSC2):c.2837+10G>T

dbSNP: rs1232454175
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics RCV001288896 SCV001476301 uncertain significance not provided 2020-06-02 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001433588 SCV001636379 likely benign Tuberous sclerosis 2 2025-01-01 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001433588 SCV002039693 likely benign Tuberous sclerosis 2 2021-11-07 criteria provided, single submitter clinical testing

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