{{Rsnum
|rsid=1502844
|Chromosome=5
|position=102523613
|Orientation=plus
|GMAF=0.3921
|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 | 15.9 | 45.1 | 38.9
| HCB | 25.7 | 52.9 | 21.3
| JPT | 30.1 | 46.0 | 23.9
| YRI | 10.2 | 45.6 | 44.2
| ASW | 8.8 | 33.3 | 57.9
| CHB | 25.7 | 52.9 | 21.3
| CHD | 27.8 | 46.3 | 25.9
| GIH | 14.0 | 51.0 | 35.0
| LWK | 9.1 | 45.5 | 45.5
| MEX | 16.1 | 39.3 | 44.6
| MKK | 14.8 | 49.0 | 36.1
| TSI | 13.7 | 50.0 | 36.3
| HapMapRevision=28
}}
{{PMID Auto GWAS
|PMID=19571808
|Trait=Schizophrenia
|Title=Common variants conferring risk of schizophrenia
|RiskAllele=C
|Pval=0.000001
|OR=1.09
|ORtxt=[NR]
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1502844
|overall_frequency_n=82
|overall_frequency_d=126
|overall_frequency=0.650794
|n_genomes=43
|n_genomes_annotated=0
|n_haplomes=69
|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 | Affy GenomeWide 6}}
{{on chip | Illumina Human 1M}}