ClinVar Miner

Submissions for variant NM_024809.5(TCTN2):c.1033+13T>A

dbSNP: rs368148687
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000243781 SCV000314447 likely benign not specified criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002058339 SCV002333782 likely benign Familial aplasia of the vermis; Meckel-Gruber syndrome 2023-11-13 criteria provided, single submitter clinical testing

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