ClinVar Miner

Submissions for variant NM_177972.3(TUB):c.397+26C>G

gnomAD frequency: 0.79455  dbSNP: rs7396690
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV002245223 SCV002514597 benign Retinal dystrophy and obesity 2021-12-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004719009 SCV005322219 benign not provided criteria provided, single submitter not provided

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