ClinVar Miner

Submissions for variant NM_000483.5(APOC2):c.255C>A (p.Tyr85Ter)

dbSNP: rs120074116
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000002701 SCV000022859 pathogenic APOLIPOPROTEIN C-II (AUCKLAND) 2003-06-01 no assertion criteria provided literature only
OMIM RCV000002702 SCV000022860 pathogenic Familial apolipoprotein C-II deficiency 2003-06-01 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.