{{Rsnum
|rsid=2601828
|Gene=ADCY9
|Chromosome=16
|position=4053870
|Orientation=minus
|GMAF=0.2975
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=ADCY9
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 4.4 | 32.7 | 62.8
| HCB | 19.9 | 46.3 | 33.8
| JPT | 19.6 | 52.7 | 27.7
| YRI | 0.7 | 34.9 | 64.4
| ASW | 5.3 | 35.1 | 59.6
| CHB | 19.9 | 46.3 | 33.8
| CHD | 17.4 | 36.7 | 45.9
| GIH | 3.0 | 31.3 | 65.7
| LWK | 1.8 | 34.9 | 63.3
| MEX | 24.6 | 45.6 | 29.8
| MKK | 3.2 | 36.1 | 60.6
| TSI | 5.0 | 32.7 | 62.4
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20522523
|Trait=Partial epilepsies
|Title=Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study
|RiskAllele=A
|Pval=0.000001
|OR=1.12
|ORtxt=[1.12-1.31]
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}