ClinVar Miner

List of variants in gene FBXL8, HSF4 studied for cataract 5 multiple types

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 12
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001538.3(HSF4):c.-944G>A rs61735433 0.04927
NM_001538.3(HSF4):c.-832G>A rs201963745 0.00162
NM_001538.3(HSF4):c.-880G>C rs201429195 0.00143
NM_001538.3(HSF4):c.-622G>C rs200404151 0.00024
NM_001538.3(HSF4):c.-772G>T rs201135322 0.00011
NM_018378.3(FBXL8):c.720A>C (p.Glu240Asp) rs768152063 0.00007
NM_001538.4(HSF4):c.-419C>T rs562489000 0.00006
NM_001538.3(HSF4):c.-874G>C rs936318443 0.00002
NM_001538.4(HSF4):c.-448A>G rs886052213 0.00002
NM_001538.3(HSF4):c.-759A>G rs777343855 0.00001
NM_001538.3(HSF4):c.-833C>T rs1332713508 0.00001
NM_001538.4(HSF4):c.-565G>A rs147591659

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.