ClinVar Miner

Submissions for variant NM_001081.4(CUBN):c.884-8T>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 RCV003838300 SCV004633943 likely benign Imerslund-Grasbeck syndrome 2022-11-08 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV004723510 SCV005340817 likely benign CUBN-related disorder 2020-02-24 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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