ClinVar Miner

Submissions for variant NM_021224.6(ZNF462):c.3076A>G (p.Thr1026Ala)

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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 RCV004546825 SCV005041640 likely benign not provided 2024-04-01 criteria provided, single submitter clinical testing ZNF462: BS1
PreventionGenetics, part of Exact Sciences RCV003914451 SCV004731056 benign ZNF462-related disorder 2019-03-22 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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