ClinVar Miner

Submissions for variant NM_001040716.2(PC):c.*13C>T

gnomAD frequency: 0.00173  dbSNP: rs58032722
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001716715 SCV001942688 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003931291 SCV004748651 likely benign PC-related disorder 2021-09-10 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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