ClinVar Miner

Submissions for variant NM_032119.4(ADGRV1):c.9907-35A>C

gnomAD frequency: 0.71289  dbSNP: rs7723259
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000833699 SCV000975463 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 RCV001701615 SCV001933924 benign Usher syndrome type 2C 2021-08-10 criteria provided, single submitter clinical testing
Genetic Services Laboratory,University of Chicago RCV000146085 SCV000193301 likely benign not specified no assertion criteria provided clinical testing

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