ClinVar Miner

Submissions for variant NM_000278.5(PAX2):c.195C>G (p.Val65=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV005038627 SCV005662261 uncertain significance Renal coloboma syndrome; Focal segmental glomerulosclerosis 7 2024-06-17 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV004534490 SCV004713326 likely benign PAX2-related disorder 2021-03-05 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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