ClinVar Miner

Submissions for variant NM_000044.6(AR):c.2607+10C>T

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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 RCV003798148 SCV004578836 benign Androgen resistance syndrome; Kennedy disease 2024-09-22 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV004755020 SCV005348874 likely benign AR-related disorder 2024-07-23 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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