ClinVar Miner

Submissions for variant NM_001039141.3(TRIOBP):c.6472+14_6472+15insT

dbSNP: rs546389039
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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 RCV002177541 SCV002346496 benign not provided 2023-01-11 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003968746 SCV004781912 likely benign TRIOBP-related disorder 2022-12-28 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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