ClinVar Miner

Submissions for variant NM_001134831.2(AHI1):c.10+115C>A

gnomAD frequency: 0.73311  dbSNP: rs9402709
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000833256 SCV000975018 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 RCV001548863 SCV001768853 benign Joubert syndrome 3 2021-07-14 criteria provided, single submitter clinical testing

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