ClinVar Miner

Submissions for variant NM_004937.3(CTNS):c.853-28C>T

gnomAD frequency: 0.00563  dbSNP: rs78671385
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000675698 SCV001785226 likely benign not provided 2020-07-11 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000675698 SCV005217955 likely benign not provided criteria provided, single submitter not provided
Mayo Clinic Laboratories, Mayo Clinic RCV000675698 SCV000801409 benign not provided 2017-06-28 no assertion criteria provided clinical testing

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