ClinVar Miner

Submissions for variant NM_018965.4(TREM2):c.417A>C (p.Gly139=)

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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 RCV005064874 SCV005693285 likely benign not provided 2024-06-13 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003954553 SCV004767899 likely benign TREM2-related disorder 2024-05-14 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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