ClinVar Miner

Submissions for variant NM_139057.4(ADAMTS17):c.2670C>T (p.Tyr890=)

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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 RCV002597182 SCV002948338 likely benign not provided 2024-09-14 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003943443 SCV004757522 likely benign ADAMTS17-related disorder 2019-04-12 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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