ClinVar Miner

Submissions for variant NM_000038.6(APC):c.136-18T>C

gnomAD frequency: 0.00001  dbSNP: rs1261769588
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV003653212 SCV002395763 likely benign Familial adenomatous polyposis 1 2024-01-05 criteria provided, single submitter clinical testing
Mayo Clinic Laboratories, Mayo Clinic RCV000583883 SCV000691702 likely benign not specified no assertion criteria provided clinical testing

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