{{Rsnum
|rsid=27388
|Gene=MEGF10
|Chromosome=5
|position=127348117
|Orientation=plus
|GMAF=0.4959
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=MEGF10
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 32.1 | 56.2 | 11.6
| HCB | 15.3 | 54.7 | 29.9
| JPT | 22.1 | 44.2 | 33.6
| YRI | 26.5 | 49.7 | 23.8
| ASW | 21.4 | 55.4 | 23.2
| CHB | 15.3 | 54.7 | 29.9
| CHD | 11.2 | 50.5 | 38.3
| GIH | 18.2 | 51.5 | 30.3
| LWK | 41.8 | 40.9 | 17.3
| MEX | 14.0 | 56.1 | 29.8
| MKK | 32.7 | 50.3 | 17.0
| TSI | 35.6 | 43.6 | 20.8
| HapMapRevision=28
}}[[rs27388]] is a SNP in the [[MEGF10]] gene.

In a case-control study involving 652 Irish patients, [[rs27388]](A) allele carriers were at increased risk for [[schizophrenia]]. (Note that the (A) allele is quite common in many populations.){{PMID|18179784|OA=1
}}

{{PMID|20813413}} No association between schizophrenia and rs27388 of the MEGF10 gene in Chinese case-control sample.

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}