ClinVar Miner

Submissions for variant NM_000038.6(APC):c.1743+193G>A

gnomAD frequency: 0.39549  dbSNP: rs351772
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001596950 SCV001830288 benign not provided 2018-06-22 criteria provided, single submitter clinical testing
Systems Biology Platform Zhejiang California International NanoSystems Institute RCV000074154 SCV000105747 cancer Familial colorectal cancer no assertion criteria provided not provided Converted during submission to other.

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