{{Rsnum
|rsid=7495052
|Gene=SLCO3A1
|Chromosome=15
|position=92008799
|Orientation=plus
|GMAF=0.477
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=SLCO3A1
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 14.2 | 50.4 | 35.4
| HCB | 55.9 | 36.8 | 7.4
| JPT | 50.0 | 38.4 | 11.6
| YRI | 9.5 | 40.1 | 50.3
| ASW | 12.3 | 45.6 | 42.1
| CHB | 55.9 | 36.8 | 7.4
| CHD | 69.7 | 28.4 | 1.8
| GIH | 19.8 | 47.5 | 32.7
| LWK | 8.3 | 46.8 | 45.0
| MEX | 27.6 | 44.8 | 27.6
| MKK | 9.8 | 45.1 | 45.1
| TSI | 19.6 | 50.0 | 30.4
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=18821565
|Trait=Inattentive symptoms
|Title=Genome-wide association scan of quantitative traits for [[attention deficit hyperactivity disorder]] identifies novel associations and confirms candidate gene associations
|RiskAllele=
|Pval=0.000003
|OR=NR
|ORtxt=NR
}}

{{PMID Auto
|PMID=20148275
|Title=Shared heritability of attention-deficit/hyperactivity disorder and autism spectrum disorder.
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs7495052
|overall_frequency_n=56
|overall_frequency_d=128
|overall_frequency=0.4375
|n_genomes=33
|n_genomes_annotated=0
|n_haplomes=45
|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 | Illumina Human 1M}}