ClinVar Miner

Submissions for variant NM_012301.4(MAGI2):c.302-9dup

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003065194 SCV003453633 benign not provided 2022-04-08 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003906466 SCV004726532 likely benign MAGI2-related disorder 2019-03-06 no assertion criteria provided clinical testing This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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