ClinVar Miner

Submissions for variant NM_031206.7(LAS1L):c.1209C>G (p.Leu403=)

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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 RCV003118705 SCV003786935 benign Wilson-Turner syndrome 2024-11-05 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003919014 SCV004733523 likely benign LAS1L-related disorder 2019-05-02 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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