{{Rsnum
|rsid=2292657
|Chromosome=12
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=GLI1
|position=57466149
|Gene_s=GLI1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 10.9 | 53.6 | 35.5
| HCB | 48.1 | 44.4 | 7.4
| JPT | 21.2 | 48.7 | 30.1
| YRI | 72.6 | 24.7 | 2.7
| ASW | 57.1 | 39.3 | 3.6
| CHB | 48.1 | 44.4 | 7.4
| CHD | 0.0 | 0.0 | 0.0
| GIH | 28.9 | 49.5 | 21.6
| LWK | 0.0 | 0.0 | 0.0
| MEX | 33.3 | 53.7 | 13.0
| MKK | 42.1 | 44.1 | 13.8
| TSI | 11.0 | 47.0 | 42.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=23792102
|Title=Phenotype variations affect genetic association studies of degenerative disc disease: conclusions of analysis of genetic association of 58 single nucleotide polymorphisms with highly specific phenotypes for disc degeneration in 332 subjects
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | Illumina Human 1M}}