{{Rsnum
|rsid=2615374
|Chromosome=8
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=KCNK9
|position=139618747
|Gene_s=KCNK9
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 14.2 | 49.6 | 36.3
| HCB | 7.3 | 36.5 | 56.2
| JPT | 8.8 | 38.9 | 52.2
| YRI | 0.7 | 21.8 | 77.6
| ASW | 1.8 | 26.3 | 71.9
| CHB | 7.3 | 36.5 | 56.2
| CHD | 15.6 | 39.4 | 45.0
| GIH | 7.9 | 49.5 | 42.6
| LWK | 0.0 | 16.4 | 83.6
| MEX | 15.5 | 37.9 | 46.6
| MKK | 0.6 | 12.8 | 86.5
| TSI | 16.7 | 48.0 | 35.3
| HapMapRevision=28
}}{{PMID Auto
|PMID=24980697
|Title=Screening individuals with intellectual disability, autism and Tourette's syndrome for KCNK9 mutations and aberrant DNA methylation within the 8q24 imprinted cluster
}}

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