ClinVar Miner

Submissions for variant NM_170784.3(MKKS):c.111T>C (p.Tyr37=)

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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 RCV002885844 SCV003242044 likely benign Bardet-Biedl syndrome; McKusick-Kaufman syndrome 2023-11-20 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV004536426 SCV004726199 likely benign MKKS-related disorder 2019-06-17 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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