ClinVar Miner

Submissions for variant NM_145868.2(ANXA11):c.1458+7G>A

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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 RCV003575972 SCV004368722 likely benign not provided 2023-03-06 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV004741640 SCV005345994 likely benign ANXA11-related disorder 2024-06-18 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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