ClinVar Miner

Submissions for variant NM_012293.3(PXDN):c.272+18A>G

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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 RCV003746291 SCV004475916 benign Anterior segment dysgenesis 7 2023-09-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004714396 SCV005283729 benign not provided criteria provided, single submitter not provided

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