ClinVar Miner

List of variants reported as likely benign for Focal segmental glomerulosclerosis by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 6
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_012120.2(CD2AP):c.*3047G>A rs116607853 0.00826
NM_004621.6(TRPC6):c.*33del rs753955901
NM_004621.6(TRPC6):c.*509_*512dup rs557577176
NM_012120.3(CD2AP):c.*1430dup rs145649247
NM_012120.3(CD2AP):c.-167_-165del rs533900030
NM_012120.3(CD2AP):c.-55_-54insAGG rs560930115

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.