ClinVar Miner

Submissions for variant NM_022124.6(CDH23):c.1135-128A>G

gnomAD frequency: 0.51167  dbSNP: rs10823810
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000838371 SCV000980237 benign not provided 2018-06-14 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.
Genome-Nilou Lab RCV001554725 SCV001776022 benign Autosomal recessive nonsyndromic hearing loss 12 2021-07-14 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001554726 SCV001776023 benign Usher syndrome type 1D 2021-07-14 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001554727 SCV001776024 benign Pituitary adenoma 5, multiple types 2021-07-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000838371 SCV005321725 benign not provided criteria provided, single submitter not provided

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