ClinVar Miner

Submissions for variant NM_031206.7(LAS1L):c.1788TGA[1] (p.Asp597del)

dbSNP: rs750470319
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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 RCV000640515 SCV000762107 benign Wilson-Turner syndrome 2024-12-11 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003905728 SCV004724918 benign LAS1L-related disorder 2023-12-15 no assertion criteria provided clinical testing This variant is classified as benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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