{{Rsnum
|rsid=5496
|Gene=ICAM1
|Chromosome=19
|position=10284771
|Orientation=plus
|GMAF=0.01377
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=ICAM1
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 100.0 | 0.0 | 0.0
| HCB | 31.1 | 42.2 | 26.7
| JPT | 36.4 | 47.7 | 15.9
| YRI | 63.5 | 33.3 | 3.2
| ASW | 0.0 | 0.0 | 0.0
| CHB | 31.1 | 42.2 | 26.7
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}
{{PMID Auto
|PMID=18420209
|Title=ICAM1 and VCAM1 polymorphisms, coronary artery calcium, and circulating levels of soluble ICAM-1: the multi-ethnic study of atherosclerosis (MESA)
|OA=1
}}

{{PMID Auto
|PMID=18528404
|Title=Variation in the ICAM1 gene is not associated with severe malaria phenotypes.
|OA=1
}}

{{PMID Auto
|PMID=19332210
|Title=Candidate genetic variants in the fibrinogen, methylenetetrahydrofolate reductase, and intercellular adhesion molecule-1 genes and plasma levels of fibrinogen, homocysteine, and intercellular adhesion molecule-1 among various race/ethnic groups: data from the Women's Genome Health Study.
|OA=1
}}

{{PMID Auto
|PMID=23137758
|Title=Genetic polymorphisms of ICAM 1 and IL28 as predictors of liver fibrosis severity and viral clearance in hepatitis C genotype 4
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}