ClinVar Miner

Submissions for variant NM_001393997.1(CCAR2):c.1845+3G>A

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV003436798 SCV004164483 likely benign not provided 2022-06-01 criteria provided, single submitter clinical testing CCAR2: BP4, BS2
PreventionGenetics, part of Exact Sciences RCV003919222 SCV004732403 benign CCAR2-related disorder 2019-06-11 no assertion criteria provided clinical testing This variant is classified as benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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