{{Rsnum
|rsid=7748513
|Gene=TREM2
|Chromosome=6
|position=41160234
|Orientation=plus
|GMAF=0.1354
|Gene_s=TREM2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 92.9 | 7.1 | 0.0
| HCB | 97.8 | 2.2 | 0.0
| JPT | 98.2 | 1.8 | 0.0
| YRI | 17.0 | 53.7 | 29.3
| ASW | 26.3 | 45.6 | 28.1
| CHB | 97.8 | 2.2 | 0.0
| CHD | 98.2 | 1.8 | 0.0
| GIH | 87.1 | 12.9 | 0.0
| LWK | 25.5 | 48.2 | 26.4
| MEX | 89.7 | 10.3 | 0.0
| MKK | 24.4 | 54.5 | 21.2
| TSI | 93.1 | 6.9 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=22939635
  |Trait=C-reactive protein
  |Title=Genome-wide association and population genetic analysis of C-reactive protein in African American and Hispanic American women.
  |RiskAllele=G
  |Pval=1E-10
  |OR=NR
  |ORtxt=NR
  |OA=1
}}

{{PMID Auto
|PMID=19019460
|Title=No evidence for shared etiology in two demyelinative disorders, MS and PLOSL.
|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}}