{{Rsnum
|rsid=1572299
|Chromosome=9
|position=118584139
|Orientation=minus
|GMAF=0.2466
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 16.8 | 54.0 | 29.2
| HCB | 100.0 | 0.0 | 0.0
| JPT | 96.5 | 3.5 | 0.0
| YRI | 94.5 | 5.5 | 0.0
| ASW | 78.9 | 21.1 | 0.0
| CHB | 100.0 | 0.0 | 0.0
| CHD | 98.1 | 1.9 | 0.0
| GIH | 60.0 | 35.0 | 5.0
| LWK | 97.2 | 2.8 | 0.0
| MEX | 49.1 | 38.6 | 12.3
| MKK | 87.0 | 13.0 | 0.0
| TSI | 19.6 | 53.9 | 26.5
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=19571808
|Trait=Schizophrenia
|Title=Common variants conferring risk of schizophrenia
|RiskAllele=A
|Pval=0.000004
|OR=1.08
|ORtxt=[NR]
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1572299
|overall_frequency_n=30
|overall_frequency_d=126
|overall_frequency=0.238095
|n_genomes=19
|n_genomes_annotated=0
|n_haplomes=25
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

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