ClinVar Miner

List of variants in gene CYP4V2 reported as benign by EGL Genetic Diagnostics, Eurofins Clinical Diagnostics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 8
Download table as spreadsheet
HGVS dbSNP
NM_207352.4(CYP4V2):c.*4T>C rs76978024
NM_207352.4(CYP4V2):c.1328G>A (p.Arg443Gln) rs72646291
NM_207352.4(CYP4V2):c.1446G>A (p.Ser482=) rs141950964
NM_207352.4(CYP4V2):c.327+11G>C rs62350517
NM_207352.4(CYP4V2):c.64C>G (p.Leu22Val) rs1055138
NM_207352.4(CYP4V2):c.802-7C>T rs3817184
NM_207352.4(CYP4V2):c.810T>G (p.Ala270=) rs3736455
NM_207352.4(CYP4V2):c.846T>C (p.Cys282=) rs3736456

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.