{{Rsnum
|rsid=2227098
|Gene=GRIA3
|Chromosome=X
|position=123361111
|Orientation=minus
|GMAF=0.4281
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=GRIA3
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 40.0 | 23.1 | 36.9
| HCB | 29.5 | 29.5 | 40.9
| JPT | 29.5 | 25.0 | 45.5
| YRI | 30.2 | 22.2 | 47.6
| ASW | 0.0 | 0.0 | 0.0
| CHB | 29.5 | 29.5 | 40.9
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}

This SNP is part of a specific haplotype, [[rs989638]]-[[rs1034428]]-[[rs2227098]] G-T-G (as oriented with respect to dbSNP) with an overall ~2x higher risk in females for [[schizophrenia]] (p=0.0008). {{PMID|18163426}}

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