ClinVar Miner

Submissions for variant NM_001127511.3(APC):c.-134_-133insG

dbSNP: rs1561393341
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003771568 SCV001727934 benign Familial adenomatous polyposis 1 2024-02-01 criteria provided, single submitter clinical testing
GeneDx RCV001562980 SCV001785839 likely benign not provided 2018-06-28 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV002476823 SCV002774334 benign not specified 2019-05-16 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV002476823 SCV004243215 benign not specified 2024-02-06 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV001562980 SCV004699067 benign not provided 2024-01-01 criteria provided, single submitter clinical testing APC: BS1, BS2

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