ClinVar Miner

Submissions for variant NM_001332.4(CTNND2):c.735CGC[7] (p.Ala251dup)

dbSNP: rs578098885
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001669276 SCV001882095 benign not provided 2018-12-26 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003975876 SCV004793947 benign CTNND2-related disorder 2022-04-06 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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