ClinVar Miner

Submissions for variant NR_046473.1(MEG3):n.936-391G>T

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV003393623 SCV004130410 likely benign not provided 2023-10-01 criteria provided, single submitter clinical testing MEG3: BS1
PreventionGenetics, part of Exact Sciences RCV003919118 SCV004729632 benign MEG3-related disorder 2019-09-20 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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