ClinVar Miner

List of variants in gene GLI3 reported as uncertain significance for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 8
Download table as spreadsheet
NM_000168.6(GLI3):c.1242+8G>A rs75925934
NM_000168.6(GLI3):c.1593T>C (p.Tyr531=) rs749798195
NM_000168.6(GLI3):c.2119C>T (p.Pro707Ser) rs121917716
NM_000168.6(GLI3):c.3098C>A (p.Pro1033Gln) rs376956433
NM_000168.6(GLI3):c.313C>T (p.Arg105Cys) rs555794809
NM_000168.6(GLI3):c.3140_3141delinsCA (p.Gln1047Pro) rs1064796326
NM_000168.6(GLI3):c.3284A>G (p.Asp1095Gly) rs1554304659
NM_000168.6(GLI3):c.3970G>C (p.Ala1324Pro) rs1480007692

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.