ClinVar Miner

Submissions for variant NM_005560.6(LAMA5):c.694G>A (p.Val232Met)

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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 RCV002959257 SCV003282958 likely benign not provided 2024-03-04 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003906403 SCV004723091 likely benign LAMA5-related disorder 2022-03-09 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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