ClinVar Miner

Submissions for variant NM_001303256.3(MORC2):c.1214+9T>C

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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 RCV003005266 SCV003301293 likely benign Charcot-Marie-Tooth disease axonal type 2Z 2024-02-13 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003926651 SCV004738913 likely benign MORC2-related disorder 2019-09-25 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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