{{Rsnum
|rsid=1444768
|Gene=KALRN
|Chromosome=3
|position=124205075
|Orientation=minus
|GMAF=0.4656
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=KALRN
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 8.8 | 46.9 | 44.2
| HCB | 27.9 | 52.2 | 19.9
| JPT | 36.3 | 40.7 | 23.0
| YRI | 75.3 | 21.9 | 2.7
| ASW | 66.7 | 24.6 | 8.8
| CHB | 27.9 | 52.2 | 19.9
| CHD | 36.1 | 38.0 | 25.9
| GIH | 26.0 | 40.0 | 34.0
| LWK | 68.2 | 29.1 | 2.7
| MEX | 13.8 | 55.2 | 31.0
| MKK | 50.0 | 44.9 | 5.1
| TSI | 12.7 | 57.8 | 29.4
| HapMapRevision=28
}}
{{PMID Auto
|PMID=19706030
|Title=Validation Study of Genetic Associations with Coronary Artery Disease on Chromosome 3q13-21 and Potential Effect Modification by Smoking
|OA=1
}}

{{PMID Auto
|PMID=17357071
|Title=Peakwide mapping on chromosome 3q13 identifies the kalirin gene as a novel candidate gene for coronary artery disease.
|OA=1
}}

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