ClinVar Miner

Submissions for variant NM_000038.6(APC):c.1744-290G>A

gnomAD frequency: 0.64971  dbSNP: rs458967
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001668177 SCV001889964 benign not provided 2019-01-10 criteria provided, single submitter clinical testing
Systems Biology Platform Zhejiang California International NanoSystems Institute RCV000074200 SCV000105793 cancer Familial colorectal cancer no assertion criteria provided not provided Converted during submission to other.

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