{{Rsnum
|rsid=6686643
|Gene=MGST3
|Chromosome=1
|position=165647351
|Orientation=plus
|GMAF=0.219
|Gene_s=MGST3,MIR302A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 8.0 | 37.2 | 54.9
| HCB | 0.0 | 4.5 | 95.5
| JPT | 0.0 | 1.8 | 98.2
| YRI | 22.4 | 55.1 | 22.4
| ASW | 16.1 | 53.6 | 30.4
| CHB | 0.0 | 4.5 | 95.5
| CHD | 0.0 | 3.7 | 96.3
| GIH | 3.0 | 28.7 | 68.3
| LWK | 21.3 | 48.1 | 30.6
| MEX | 5.2 | 19.0 | 75.9
| MKK | 13.5 | 45.2 | 41.3
| TSI | 3.9 | 29.4 | 66.7
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21116278
|Trait=None
|Title=Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease
|RiskAllele=
|Pval=0.000007
|OR=0.0032
|ORtxt=[NR] unit increase (main effect)
}}

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