ClinVar Miner

Submissions for variant NM_006885.4(ZFHX3):c.3870C>T (p.Thr1290=)

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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 RCV003419443 SCV004144985 benign not provided 2022-10-01 criteria provided, single submitter clinical testing ZFHX3: BS1, BS2
PreventionGenetics, part of Exact Sciences RCV003966370 SCV004785219 likely benign ZFHX3-related disorder 2019-08-16 no assertion criteria provided clinical testing This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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