ClinVar Miner

List of variants in gene CYP4V2, LOC129993526 studied for corneal disorder

Included ClinVar conditions (75):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 10
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_207352.4(CYP4V2):c.64C>G (p.Leu22Val) rs1055138 0.46276
NM_207352.4(CYP4V2):c.-146C>T rs1398007 0.41622
NM_207352.4(CYP4V2):c.-152A>G rs2241819 0.39682
NM_207352.4(CYP4V2):c.-128A>G rs531909464 0.01113
NM_207352.4(CYP4V2):c.24C>T (p.Leu8=) rs202148693 0.00077
NM_207352.4(CYP4V2):c.-178C>T rs886059279 0.00009
NM_207352.4(CYP4V2):c.-22C>G rs894067959 0.00002
NM_207352.4(CYP4V2):c.-133G>T rs562885669
NM_207352.4(CYP4V2):c.-199C>T rs886059278
NM_207352.4(CYP4V2):c.-56C>G rs886059280

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.