{{Rsnum
|rsid=7544736
|Chromosome=1
|position=96698787
|Orientation=plus
|GMAF=0.2296
|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 | 66.4 | 29.2 | 4.4
| HCB | 67.2 | 32.8 | 0.0
| JPT | 61.1 | 35.4 | 3.5
| YRI | 34.2 | 50.0 | 15.8
| ASW | 43.9 | 43.9 | 12.3
| CHB | 67.2 | 32.8 | 0.0
| CHD | 63.9 | 29.6 | 6.5
| GIH | 63.4 | 33.7 | 3.0
| LWK | 50.9 | 31.8 | 17.3
| MEX | 67.2 | 29.3 | 3.4
| MKK | 37.2 | 45.5 | 17.3
| TSI | 54.9 | 40.2 | 4.9
| HapMapRevision=28
}}
{{PMID Auto GWAS
|PMID=19571811
|Trait=Schizophrenia
|Title=Common polygenic variation contributes to risk of schizophrenia and bipolar disorder
|RiskAllele=G
|Pval=6E-7
|OR=1.25
|ORtxt=None
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs7544736
|overall_frequency_n=29
|overall_frequency_d=128
|overall_frequency=0.226562
|n_genomes=22
|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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}