ClinVar Miner

List of variants in gene FBXO7 reported as benign for Parkinson disease 15

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 4
Download table as spreadsheet
NM_012179.4(FBXO7):c.122+272T>G rs8137714
NM_012179.4(FBXO7):c.345G>A (p.Met115Ile) rs11107
NM_012179.4(FBXO7):c.540A>G (p.Pro180=) rs41311141
NM_012179.4(FBXO7):c.949C>T (p.Leu317=) rs9726

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.