ClinVar Miner

Submissions for variant NM_000511.6(FUT2):c.461G>A (p.Trp154Ter)

gnomAD frequency: 0.45281  dbSNP: rs601338
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 5
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV002490360 SCV002799025 benign Vitamin b12 plasma level quantitative trait locus 1; Bombay phenotype 2021-08-12 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004716906 SCV005313405 benign not provided criteria provided, single submitter not provided
OMIM RCV000013808 SCV000034055 benign SECRETOR/NONSECRETOR POLYMORPHISM 2008-10-01 no assertion criteria provided literature only
OMIM RCV000013810 SCV000034057 association Vitamin b12 plasma level quantitative trait locus 1 2008-10-01 no assertion criteria provided literature only
University of Washington Center for Mendelian Genomics, University of Washington RCV001291126 SCV001479492 confers sensitivity Familial Otitis Media no assertion criteria provided research

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.