ClinVar Miner

Submissions for variant NM_001160372.4(TRAPPC9):c.1768+7C>T

gnomAD frequency: 0.00003  dbSNP: rs587780485
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000118669 SCV000153083 uncertain significance not provided 2014-02-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000118669 SCV004538571 likely benign not provided 2023-11-18 criteria provided, single submitter clinical testing

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