ClinVar Miner

Submissions for variant NM_001282933.2(ZNF341):c.1035C>T (p.Thr345=)

dbSNP: rs192880441
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001511924 SCV001719248 benign not provided 2024-01-14 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003966067 SCV004779268 likely benign ZNF341-related disorder 2023-11-22 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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