ClinVar Miner

Submissions for variant NM_000038.5(APC):c.1958+8T>C (rs62626346)

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 10
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV000077982 SCV000602529 benign not specified 2017-05-01 criteria provided, single submitter clinical testing
Color RCV000579978 SCV000681498 benign Hereditary cancer-predisposing syndrome 2016-03-21 criteria provided, single submitter clinical testing
Department of Pathology and Laboratory Medicine,Sinai Health System RCV000077982 SCV000591100 benign not specified 2013-03-04 criteria provided, single submitter clinical testing
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000077982 SCV000109813 benign not specified 2012-10-26 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000379464 SCV000451993 likely benign APC-Associated Polyposis Disorders 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000477032 SCV000562613 benign Familial adenomatous polyposis 1 2017-08-18 criteria provided, single submitter clinical testing
Mayo Clinic Genetic Testing Laboratories,Mayo Clinic RCV000077982 SCV000256935 benign not specified no assertion criteria provided clinical testing
PreventionGenetics RCV000077982 SCV000301589 benign not specified criteria provided, single submitter clinical testing
Systems Biology Platform Zhejiang California International NanoSystems Institute RCV000073605 SCV000105196 cancer Familial colorectal cancer no assertion criteria provided not provided Converted during submission to other.
True Health Diagnostics RCV000579978 SCV000693472 likely benign Hereditary cancer-predisposing syndrome 2017-09-29 no assertion criteria provided clinical testing

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.