{{Rsnum
|rsid=757863
|Gene=MAGI2
|Chromosome=7
|position=78042064
|Orientation=plus
|GMAF=0.3838
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=MAGI2
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 25.7 | 55.8 | 18.6
| HCB | 57.7 | 40.1 | 2.2
| JPT | 49.6 | 39.8 | 10.6
| YRI | 27.2 | 53.1 | 19.7
| ASW | 24.6 | 52.6 | 22.8
| CHB | 57.7 | 40.1 | 2.2
| CHD | 56.0 | 39.4 | 4.6
| GIH | 51.5 | 35.6 | 12.9
| LWK | 24.5 | 46.4 | 29.1
| MEX | 55.2 | 34.5 | 10.3
| MKK | 25.6 | 55.1 | 19.2
| TSI | 25.5 | 52.9 | 21.6
| HapMapRevision=28
}}This SNP was associated with amyotrophic lateral sclerosis ([[ALS]]) based on a study of 1,152 patients.{{PMID|17671248}}

{{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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}