ClinVar Miner

Submissions for variant NM_000038.6(APC):c.-19+734C>T

gnomAD frequency: 0.51721  dbSNP: rs2020383
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001811348 SCV001472384 benign not provided 2022-09-13 criteria provided, single submitter clinical testing
Systems Biology Platform Zhejiang California International NanoSystems Institute RCV000073733 SCV000105324 cancer Familial colorectal cancer no assertion criteria provided not provided Converted during submission to other.

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