{{Rsnum
|rsid=6079395
|Gene=MACROD2
|Chromosome=20
|position=14347253
|Orientation=plus
|GMAF=0.404
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=MACROD2
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 35.4 | 48.7 | 15.9
| HCB | 0.0 | 28.5 | 71.5
| JPT | 3.5 | 28.3 | 68.1
| YRI | 22.4 | 42.9 | 34.7
| ASW | 19.3 | 35.1 | 45.6
| CHB | 0.0 | 28.5 | 71.5
| CHD | 8.3 | 33.0 | 58.7
| GIH | 5.9 | 32.7 | 61.4
| LWK | 20.0 | 48.2 | 31.8
| MEX | 13.8 | 51.7 | 34.5
| MKK | 12.2 | 50.6 | 37.2
| TSI | 29.4 | 46.1 | 24.5
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20708005
|Trait=None
|Title=Genome-Wide Association Study Identifies Variants Associated with Histologic Features of Nonalcoholic Fatty Liver Disease
|RiskAllele=A
|Pval=0.000007
|OR=0.92
|ORtxt=[NR] unit increase
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}