{{Rsnum
|rsid=10134944
|Gene=SLC35F4
|Chromosome=14
|position=57652478
|Orientation=plus
|GMAF=0.1506
|Gene_s=SLC35F4
|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 | 83.9 | 16.1 | 0.0
| HCB | 65.4 | 30.1 | 4.4
| JPT | 62.5 | 30.4 | 7.1
| YRI | 58.5 | 39.5 | 2.0
| ASW | 51.8 | 41.1 | 7.1
| CHB | 65.4 | 30.1 | 4.4
| CHD | 0.0 | 0.0 | 0.0
| GIH | 73.3 | 23.8 | 3.0
| LWK | 62.6 | 26.2 | 11.2
| MEX | 82.8 | 17.2 | 0.0
| MKK | 77.4 | 21.3 | 1.3
| TSI | 81.4 | 17.6 | 1.0
| HapMapRevision=28
}}[[rs10134944]] 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 1.45 (CI 1.24-1.68), and for homozygotes, 1.32 (CI 0.74-2.33). {{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=0.000001
|OR=None
|ORtxt=None
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs10134944
|overall_frequency_n=18
|overall_frequency_d=128
|overall_frequency=0.140625
|n_genomes=14
|n_genomes_annotated=0
|n_haplomes=16
|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}}