ClinVar Miner

Submissions for variant NM_153033.5(KCTD7):c.315-24C>T

gnomAD frequency: 0.01333  dbSNP: rs75672175
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000675798 SCV001881884 benign not provided 2018-06-28 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000675798 SCV005270727 benign not provided criteria provided, single submitter not provided
Mayo Clinic Laboratories, Mayo Clinic RCV000675798 SCV000801519 likely benign not provided 2015-10-26 no assertion criteria provided clinical testing

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