ClinVar Miner

Submissions for variant NM_000038.6(APC):c.729+31A>G

gnomAD frequency: 0.00007  dbSNP: rs374626709
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV000202000 SCV004243226 likely benign not specified 2024-02-06 criteria provided, single submitter clinical testing
Mayo Clinic Laboratories, Mayo Clinic RCV000202000 SCV000257029 likely benign not specified no assertion criteria provided research

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