{{Rsnum
|rsid=1344484
|Chromosome=16
|position=52878387
|Orientation=plus
|GMAF=0.4784
|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 | 9.7 | 49.6 | 40.7
| HCB | 37.2 | 52.6 | 10.2
| JPT | 23.9 | 53.1 | 23.0
| YRI | 24.5 | 45.6 | 29.9
| ASW | 21.1 | 49.1 | 29.8
| CHB | 37.2 | 52.6 | 10.2
| CHD | 29.4 | 56.9 | 13.8
| GIH | 19.8 | 48.5 | 31.7
| LWK | 25.5 | 40.9 | 33.6
| MEX | 32.8 | 53.4 | 13.8
| MKK | 6.4 | 46.8 | 46.8
| TSI | 12.7 | 48.0 | 39.2
| HapMapRevision=28
}}
[[rs1344484]] has been reported in a large study to be associated with [[bipolar disorder]].

The risk allele (oriented to the dbSNP entry) is (T); the odds ratio associated with heterozygotes is 1.24 (CI 1.03-1.48), and for homozygotes, 1.52 (CI 1.27-1.82). {{PMID|17554300|OA=1
}}

{{PMID Auto GWAS
|PMID=21254220
|Trait=None
|Title=Propensity score-based nonparametric test revealing genetic variants underlying bipolar disorder.
|RiskAllele=
|Pval=0.000002
|OR=None
|ORtxt=None
|OA=1
}}

{{PMID|19308021|OA=1
}} Findings from bipolar disorder genome-wide association studies replicate in a Finnish bipolar family-cohort.

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}