ClinVar Miner

Submissions for variant NM_000038.6(APC):c.645+32C>T

gnomAD frequency: 0.06662  dbSNP: rs2909961
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000202160 SCV000301603 benign not specified criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001711978 SCV000602505 benign not provided 2020-04-15 criteria provided, single submitter clinical testing
GeneDx RCV001711978 SCV001943935 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
KCCC/NGS Laboratory, Kuwait Cancer Control Center RCV004563124 SCV004017516 benign Familial adenomatous polyposis 1 2023-07-07 criteria provided, single submitter clinical testing
Mayo Clinic Laboratories, Mayo Clinic RCV000202160 SCV000257025 benign not specified no assertion criteria provided research

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