ClinVar Miner

Submissions for variant NM_033360.4(KRAS):c.*671C>T

dbSNP: rs566222739
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000290817 SCV000377724 uncertain significance Noonan syndrome 2016-06-14 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory, The Hospital for Sick Children RCV001813460 SCV002060524 likely benign Noonan syndrome and Noonan-related syndrome 2016-12-22 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003391096 SCV004134570 likely benign not provided 2022-12-01 criteria provided, single submitter clinical testing KRAS: BS1

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.