ClinVar Miner

Submissions for variant NM_001135998.3(NDUFB11):c.198G>A (p.Leu66=)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV003944067 SCV004764677 likely benign NDUFB11-related disorders 2022-02-15 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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