ClinVar Miner

Submissions for variant NM_000038.6(APC):c.136-230C>A

gnomAD frequency: 0.65666  dbSNP: rs2464805
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001610344 SCV001841114 benign not provided 2018-06-22 criteria provided, single submitter clinical testing
Systems Biology Platform Zhejiang California International NanoSystems Institute RCV000073860 SCV000105453 cancer Familial colorectal cancer no assertion criteria provided not provided Converted during submission to other.

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