ClinVar Miner

Submissions for variant NM_000129.3(F13A1):c.103G>T (p.Val35Leu) (rs5985)

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 4
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000374698 SCV000464379 likely benign Factor XIII subunit A deficiency 2016-06-14 criteria provided, single submitter clinical testing
OMIM RCV000017996 SCV000038275 protective Myocardial infarction, protection against 2007-04-01 no assertion criteria provided literature only
OMIM RCV000017997 SCV000038276 protective Venous thrombosis, protection against 2007-04-01 no assertion criteria provided literature only
PreventionGenetics RCV000248039 SCV000302397 benign not specified criteria provided, single submitter 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.