{{Rsnum
|rsid=11622475
|Gene=TDRD9
|Chromosome=14
|position=104042739
|Orientation=plus
|GMAF=0.2314
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=TDRD9
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 58.2 | 33.6 | 8.2
| HCB | 54.1 | 39.3 | 6.7
| JPT | 46.9 | 44.2 | 8.8
| YRI | 95.9 | 4.1 | 0.0
| ASW | 80.7 | 19.3 | 0.0
| CHB | 54.1 | 39.3 | 6.7
| CHD | 47.7 | 48.6 | 3.7
| GIH | 31.0 | 47.0 | 22.0
| LWK | 94.5 | 4.5 | 0.9
| MEX | 50.0 | 34.5 | 15.5
| MKK | 88.3 | 11.7 | 0.0
| TSI | 41.6 | 47.5 | 10.9
| HapMapRevision=28
}}[[rs11622475]] has been reported in a large study to be associated with [[bipolar disorder]].

The risk allele (oriented to the dbSNP entry) is (C); the odds ratio associated with heterozygotes is 1.13 (CI 0.89-1.44), and for homozygotes, 1.47 (CI 1.17-1.86). {{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 Auto
|PMID=19308021
|Title=Findings from bipolar disorder genome-wide association studies replicate in a Finnish bipolar family-cohort.
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs11622475
|overall_frequency_n=41
|overall_frequency_d=128
|overall_frequency=0.320312
|n_genomes=28
|n_genomes_annotated=0
|n_haplomes=35
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}