ClinVar Miner

Submissions for variant NM_001070.5(TUBG1):c.50-15G>T

gnomAD frequency: 0.00139  dbSNP: rs16967891
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001555444 SCV001776865 likely benign not provided 2018-09-18 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001555444 SCV003033466 benign not provided 2023-07-26 criteria provided, single submitter clinical testing

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