{{Rsnum
|rsid=10793294
|Gene=GAB2
|Chromosome=11
|position=78285357
|Orientation=plus
|GMAF=0.4876
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=GAB2
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 66.4 | 31.9 | 1.8
| HCB | 4.4 | 36.5 | 59.1
| JPT | 0.9 | 37.2 | 61.9
| YRI | 13.6 | 46.9 | 39.5
| ASW | 16.1 | 46.4 | 37.5
| CHB | 4.4 | 36.5 | 59.1
| CHD | 3.7 | 35.2 | 61.1
| GIH | 15.8 | 52.5 | 31.7
| LWK | 15.5 | 50.9 | 33.6
| MEX | 31.0 | 50.0 | 19.0
| MKK | 9.6 | 48.7 | 41.7
| TSI | 49.0 | 46.1 | 4.9
| HapMapRevision=28
}}{{PMID Auto
|PMID=21108942
|Title=Common variant in GRB2 is associated with late-onset Alzheimer's disease in Han Chinese
}}

{{PMID|17553421|OA=1
}} GAB2 alleles modify Alzheimer's risk in APOE epsilon4 carriers.

{{PMID Auto
|PMID=23071633
|Title=Mining pure, strict epistatic interactions from high-dimensional datasets: ameliorating the curse of dimensionality.
|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}