ClinVar Miner

List of variants studied for syndromic dyslipidemia by GBinsight Genetic Testing by GB HealthWatch, Genben Lifesciences Corporation

Included ClinVar conditions (70):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 2
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000237.3(LPL):c.929G>A (p.Cys310Tyr) rs1409123950 0.00001
NM_178172.6(GPIHBP1):c.230G>A (p.Cys77Tyr) rs780340378

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.