ClinVar Miner

Submissions for variant NM_025179.4(PLXNA2):c.1413G>A (p.Glu471=)

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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 RCV002937787 SCV003259637 benign not provided 2024-01-06 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003961218 SCV004778501 likely benign PLXNA2-related disorder 2021-06-17 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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