{{Rsnum
|rsid=5742612
|Gene=IGF1
|Chromosome=12
|position=102481086
|Orientation=minus
|GMAF=0.1166
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=IGF1
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 0.0 | 4.4 | 95.6
| HCB | 5.8 | 47.4 | 46.7
| JPT | 8.8 | 32.7 | 58.4
| YRI | 0.0 | 7.5 | 92.5
| ASW | 0.0 | 7.0 | 93.0
| CHB | 5.8 | 47.4 | 46.7
| CHD | 9.2 | 55.0 | 35.8
| GIH | 1.0 | 20.8 | 78.2
| LWK | 0.0 | 2.7 | 97.3
| MEX | 3.4 | 27.6 | 69.0
| MKK | 0.0 | 4.5 | 95.5
| TSI | 0.0 | 6.9 | 93.1
| HapMapRevision=28
}}{{PMID Auto
|PMID=18761080
|Title=Absence of association between SNPs in the promoter region of the insulin-like growth factor 1 (IGF-1) gene and longevity in the Han Chinese population
}}

{{PMID Auto
|PMID=17108398
|Title=Genetic association study of insulin-like growth factor-I (IGF-I) gene with curve severity and osteopenia in adolescent idiopathic scoliosis.
}}

{{PMID Auto
|PMID=18398040
|Title=Transcription factor 7-like 2 polymorphism and colon cancer.
|OA=1
}}

{{PMID Auto
|PMID=18992263
|Title=Colon tumor mutations and epigenetic changes associated with genetic polymorphism: insight into disease pathways.
|OA=1
}}

{{PMID Auto
|PMID=19240240
|Title=IGF-I and IGFBP-3 polymorphisms in relation to circulating levels among African American and Caucasian women.
|OA=1
}}

{{PMID Auto
|PMID=20199671
|Title=A microsatellite polymorphism in IGF1 gene promoter and longevity in a Han Chinese population.
|OA=1
}}

{{PMID Auto
|PMID=21046444
|Title=Are elevated levels of IGF-1 caused by coronary arteriesoclerosis?: Molecular and clinical analysis.
|OA=1
}}

{{PMID Auto
|PMID=21113804
|Title=IGF1 htSNPs in relation to IGF-1 levels in young women from high-risk breast cancer families: implications for early-onset breast cancer.
}}

{{PMID Auto
|PMID=23757194
|Title=Functional Interaction between SNPs and Microsatellite in the Transcriptional Regulation of Insulin-Like Growth Factor 1
}}

{{PMID Auto
|PMID=23364988
|Title=Analysis of single nucleotide polymorphism in adolescent idiopathic scoliosis in Korea: for personalized treatment.
|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}