ClinVar Miner

Submissions for variant NM_033026.6(PCLO):c.15289-5dup

dbSNP: rs779490171
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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 RCV002103896 SCV002394933 benign not provided 2023-01-24 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003968890 SCV004785656 likely benign PCLO-related disorder 2022-09-07 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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