ClinVar Miner

Submissions for variant NM_017449.5(EPHB2):c.835G>T (p.Ala279Ser)

gnomAD frequency: 0.00424  dbSNP: rs35882952
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
Labcorp Genetics (formerly Invitae), Labcorp RCV000894397 SCV001038378 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000894397 SCV005282019 benign not provided criteria provided, single submitter not provided
OMIM RCV000009059 SCV000029276 pathogenic Prostate cancer/brain cancer susceptibility 2004-09-01 no assertion criteria provided literature only

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.