ClinVar Miner

List of variants reported as benign for Fraser syndrome 3

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 12
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001366722.1(GRIP1):c.2464+15T>C rs7970076 0.97982
NM_001366722.1(GRIP1):c.2461C>G (p.Gln821Glu) rs13277 0.87545
NM_001366722.1(GRIP1):c.724+10G>A rs12316942 0.67684
NM_001366722.1(GRIP1):c.1838+13G>T rs7397862 0.49975
NM_001366722.1(GRIP1):c.*616T>C rs1168308 0.47053
NM_001366722.1(GRIP1):c.503-15C>A rs11838180 0.27190
NM_001366722.1(GRIP1):c.418+26A>G rs66522623 0.25360
NM_001366722.1(GRIP1):c.*428C>T rs78619935 0.00225
NM_001366722.1(GRIP1):c.1199-7C>G rs200313638 0.00029
NM_001366722.1(GRIP1):c.692C>T (p.Ala231Val) rs150958775 0.00029
NM_001366722.1(GRIP1):c.418+14C>A rs79994510
NM_001366722.1(GRIP1):c.964G>A (p.Ala322Thr) rs17102531

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.