ClinVar Miner

Submissions for variant NM_001082538.3(TCTN1):c.473-10dup

dbSNP: rs771463400
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001518783 SCV001727542 benign Familial aplasia of the vermis; Meckel-Gruber syndrome 2024-05-31 criteria provided, single submitter clinical testing
GeneDx RCV001581170 SCV001811192 likely benign not provided 2018-11-02 criteria provided, single submitter clinical testing

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