ClinVar Miner

Submissions for variant NM_006231.4(POLE):c.6658-18G>A

gnomAD frequency: 0.00002  dbSNP: rs575414442
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003657528 SCV002224018 likely benign not provided 2025-01-12 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV003321885 SCV004027282 likely benign not specified 2025-03-04 criteria provided, single submitter clinical testing

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