ClinVar Miner

Submissions for variant NM_152513.4(MEI1):c.3772G>T (p.Asp1258Tyr)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Yatsenko Laboratory, Magee-Womens Research Institute, University of Pittsburgh RCV003149079 SCV003836557 likely pathogenic Hydatidiform mole, recurrent, 3 2022-12-30 criteria provided, single submitter research
PreventionGenetics, part of Exact Sciences RCV003936713 SCV004755458 benign MEI1-related disorder 2019-09-12 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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