ClinVar Miner

Submissions for variant NM_177972.3(TUB):c.885+7T>C

dbSNP: rs776753352
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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 RCV002071369 SCV002328854 likely benign not provided 2022-05-17 criteria provided, single submitter clinical testing
New York Genome Center RCV002468388 SCV002764512 uncertain significance Retinal dystrophy and obesity 2021-12-29 criteria provided, single submitter clinical testing

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