ClinVar Miner

Submissions for variant NM_024721.5(ZFHX4):c.196G>A (p.Val66Ile)

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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 RCV003423943 SCV004155947 likely benign not provided 2024-01-01 criteria provided, single submitter clinical testing ZFHX4: BP4, BS2
PreventionGenetics, part of Exact Sciences RCV003939027 SCV004753383 benign ZFHX4-related disorder 2019-03-11 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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