ClinVar Miner

Submissions for variant NM_024870.4(PREX2):c.-4G>C

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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 RCV003435520 SCV004155923 likely benign not provided 2022-11-01 criteria provided, single submitter clinical testing PREX2: BP4, BS2
PreventionGenetics, part of Exact Sciences RCV003980946 SCV004789053 benign PREX2-related disorder 2019-02-18 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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