ClinVar Miner

Submissions for variant NM_000038.6(APC):c.729+88T>C

gnomAD frequency: 0.00237  dbSNP: rs79627325
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001711168 SCV001943934 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Systems Biology Platform Zhejiang California International NanoSystems Institute RCV000073469 SCV000105060 cancer Familial colorectal cancer no assertion criteria provided not provided Converted during submission to other.

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