{{Rsnum
|rsid=2306801
|Gene=KCNN4
|Chromosome=19
|position=43776326
|Orientation=plus
|GMAF=0.1354
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=KCNN4
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.9 | 34.5 | 64.6
| HCB | 1.5 | 16.8 | 81.8
| JPT | 3.5 | 23.9 | 72.6
| YRI | 0.7 | 25.2 | 74.1
| ASW | 1.8 | 19.3 | 78.9
| CHB | 1.5 | 16.8 | 81.8
| CHD | 0.9 | 30.3 | 68.8
| GIH | 2.0 | 35.6 | 62.4
| LWK | 0.9 | 26.4 | 72.7
| MEX | 3.4 | 19.0 | 77.6
| MKK | 2.6 | 24.4 | 73.1
| TSI | 1.0 | 30.4 | 68.6
| HapMapRevision=28
}}
{{PMID Auto
|PMID=19644414
|Title=Relationship between haplotypes of KCNN4 gene and susceptibility to human vascular diseases in Japanese
}}

{{PMID Auto
|PMID=20407432
|Title=KCNN4 Gene Variant Is Associated With Ileal Crohn's Disease in the Australian and New Zealand Population
}}

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