ClinVar Miner

Submissions for variant NM_015021.3(ZNF292):c.3667C>G (p.Gln1223Glu)

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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 RCV003885150 SCV004700961 likely benign not provided 2023-12-01 criteria provided, single submitter clinical testing ZNF292: BP4, BS1
PreventionGenetics, part of Exact Sciences RCV003949098 SCV004767144 benign ZNF292-related disorder 2021-06-25 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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