{{Rsnum
|rsid=648202
|Gene=KL
|Chromosome=13
|position=33061326
|Orientation=plus
|GMAF=0.27
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=KL
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 72.6 | 25.7 | 1.8
| HCB | 39.4 | 48.2 | 12.4
| JPT | 46.9 | 41.6 | 11.5
| YRI | 26.5 | 46.9 | 26.5
| ASW | 54.4 | 31.6 | 14.0
| CHB | 39.4 | 48.2 | 12.4
| CHD | 38.5 | 45.0 | 16.5
| GIH | 65.3 | 29.7 | 5.0
| LWK | 24.5 | 54.5 | 20.9
| MEX | 65.5 | 31.0 | 3.4
| MKK | 32.1 | 44.2 | 23.7
| TSI | 83.3 | 14.7 | 2.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=20394945
|Title=Infantile hypercalcemia and hypercalciuria: new insights into a vitamin D-dependent mechanism and response to ketoconazole treatment
}}

{{PMID Auto
|PMID=20401335
|Title=Sickle Cell Disease in the Post Genomic Era: A Monogenic Disease with a Polygenic Phenotype.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}