ClinVar Miner

Submissions for variant NM_000038.6(APC):c.645+50A>G

gnomAD frequency: 0.00009  dbSNP: rs377697545
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001549984 SCV001770235 likely benign not provided 2018-06-21 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV002268512 SCV002550568 benign not specified 2023-08-15 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001549984 SCV005226769 likely benign not provided criteria provided, single submitter not provided

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