ClinVar Miner

Submissions for variant NM_023067.4(FOXL2):c.762G>A (p.Ser254=)

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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 RCV002720083 SCV002995979 benign not provided 2023-08-14 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003916513 SCV004734180 likely benign FOXL2-related disorder 2019-05-03 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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