ClinVar Miner

Submissions for variant NM_173660.5(DOK7):c.-30G>T

gnomAD frequency: 0.11265  dbSNP: rs146168804
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000252814 SCV000316506 likely benign not specified criteria provided, single submitter clinical testing
GeneDx RCV000252814 SCV000519820 benign not specified 2016-05-20 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Breakthrough Genomics, Breakthrough Genomics RCV004710678 SCV005256607 likely benign not provided criteria provided, single submitter not provided

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